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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Psychiatry</journal-id>
<journal-title>Frontiers in Psychiatry</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Psychiatry</abbrev-journal-title>
<issn pub-type="epub">1664-0640</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fpsyt.2021.767571</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Psychiatry</subject>
<subj-group>
<subject>Original Research</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Longitudinal Bidirectional Relationships Between Maternal Depressive/Anxious Symptoms and Children&#x00027;s Tic Frequency in Early Adolescence</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name><surname>Yagi</surname> <given-names>Tomoko</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="corresp" rid="c001"><sup>&#x0002A;</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/1375801/overview"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Ando</surname> <given-names>Shuntaro</given-names></name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<xref ref-type="aff" rid="aff3"><sup>3</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/1380968/overview"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Usami</surname> <given-names>Satoshi</given-names></name>
<xref ref-type="aff" rid="aff4"><sup>4</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/667196/overview"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Yamasaki</surname> <given-names>Syudo</given-names></name>
<xref ref-type="aff" rid="aff3"><sup>3</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/1010875/overview"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Morita</surname> <given-names>Masaya</given-names></name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Kiyono</surname> <given-names>Tomoki</given-names></name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/1534097/overview"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Hayashi</surname> <given-names>Noriyuki</given-names></name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Endo</surname> <given-names>Kaori</given-names></name>
<xref ref-type="aff" rid="aff3"><sup>3</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/1047521/overview"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Iijima</surname> <given-names>Yudai</given-names></name>
<xref ref-type="aff" rid="aff3"><sup>3</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Morimoto</surname> <given-names>Yuko</given-names></name>
<xref ref-type="aff" rid="aff5"><sup>5</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/184931/overview"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Kanata</surname> <given-names>Sho</given-names></name>
<xref ref-type="aff" rid="aff6"><sup>6</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Fujikawa</surname> <given-names>Shinya</given-names></name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<xref ref-type="aff" rid="aff7"><sup>7</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Koike</surname> <given-names>Shinsuke</given-names></name>
<xref ref-type="aff" rid="aff8"><sup>8</sup></xref>
<xref ref-type="aff" rid="aff9"><sup>9</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/89045/overview"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Kano</surname> <given-names>Yukiko</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/1418109/overview"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Hiraiwa-Hasegawa</surname> <given-names>Mariko</given-names></name>
<xref ref-type="aff" rid="aff5"><sup>5</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Nishida</surname> <given-names>Atsushi</given-names></name>
<xref ref-type="aff" rid="aff3"><sup>3</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/1057779/overview"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Kasai</surname> <given-names>Kiyoto</given-names></name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<xref ref-type="aff" rid="aff9"><sup>9</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/1472170/overview"/>
</contrib>
</contrib-group>
<aff id="aff1"><sup>1</sup><institution>Department of Child Neuropsychiatry, Graduate School of Medicine, The University of Tokyo</institution>, <addr-line>Tokyo</addr-line>, <country>Japan</country></aff>
<aff id="aff2"><sup>2</sup><institution>Department of Neuropsychiatry, Graduate School of Medicine, The University of Tokyo</institution>, <addr-line>Tokyo</addr-line>, <country>Japan</country></aff>
<aff id="aff3"><sup>3</sup><institution>Department of Psychiatry and Behavioural Sciences, Tokyo Metropolitan Institute of Medical Science</institution>, <addr-line>Tokyo</addr-line>, <country>Japan</country></aff>
<aff id="aff4"><sup>4</sup><institution>Graduate School of Education, The University of Tokyo</institution>, <addr-line>Tokyo</addr-line>, <country>Japan</country></aff>
<aff id="aff5"><sup>5</sup><institution>Department of Evolutionary Studies of Biosystems, School of Advanced Sciences, SOKENDAI (The Graduate University for Advanced Studies)</institution>, <addr-line>Hayama</addr-line>, <country>Japan</country></aff>
<aff id="aff6"><sup>6</sup><institution>Department of Psychiatry, Teikyo University School of Medicine</institution>, <addr-line>Tokyo</addr-line>, <country>Japan</country></aff>
<aff id="aff7"><sup>7</sup><institution>Centre for Adolescent Health, Murdoch Children&#x00027;s Research Institute</institution>, <addr-line>Melbourne, VIC</addr-line>, <country>Australia</country></aff>
<aff id="aff8"><sup>8</sup><institution>University of Tokyo Institute for Diversity and Adaptation of Human Mind, The University of Tokyo</institution>, <addr-line>Tokyo</addr-line>, <country>Japan</country></aff>
<aff id="aff9"><sup>9</sup><institution>The International Research Center for Neurointelligence (WPI-IRCN), The University of Tokyo Institutes for Advanced Study (UTIAS)</institution>, <addr-line>Tokyo</addr-line>, <country>Japan</country></aff>
<author-notes>
<fn fn-type="edited-by"><p>Edited by: Takeo Fujiwara, Tokyo Medical and Dental University, Japan</p></fn>
<fn fn-type="edited-by"><p>Reviewed by: Say How Ong, Institute of Mental Health, Singapore; Diego Gomez-Baya, University of Huelva, Spain</p></fn>
<corresp id="c001">&#x0002A;Correspondence: Tomoko Yagi <email>tomoko-yagi&#x00040;umin.ac.jp</email></corresp>
<fn fn-type="other" id="fn001"><p>This article was submitted to Child and Adolescent Psychiatry, a section of the journal Frontiers in Psychiatry</p></fn></author-notes>
<pub-date pub-type="epub">
<day>24</day>
<month>11</month>
<year>2021</year>
</pub-date>
<pub-date pub-type="collection">
<year>2021</year>
</pub-date>
<volume>12</volume>
<elocation-id>767571</elocation-id>
<history>
<date date-type="received">
<day>31</day>
<month>08</month>
<year>2021</year>
</date>
<date date-type="accepted">
<day>01</day>
<month>11</month>
<year>2021</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x000A9; 2021 Yagi, Ando, Usami, Yamasaki, Morita, Kiyono, Hayashi, Endo, Iijima, Morimoto, Kanata, Fujikawa, Koike, Kano, Hiraiwa-Hasegawa, Nishida and Kasai.</copyright-statement>
<copyright-year>2021</copyright-year>
<copyright-holder>Yagi, Ando, Usami, Yamasaki, Morita, Kiyono, Hayashi, Endo, Iijima, Morimoto, Kanata, Fujikawa, Koike, Kano, Hiraiwa-Hasegawa, Nishida and Kasai</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/"><p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p></license> </permissions>
<abstract><p><bold>Background:</bold> Previous studies have revealed an association between maternal depressive/anxious symptoms and children&#x00027;s tics. However, the longitudinal relationships between these symptoms remain unclear. We examined the longitudinal relationships between maternal depressive/anxious symptoms and children&#x00027;s tic frequency in early adolescence with a population-based sample.</p>
<p><bold>Methods:</bold> The participants consisted of 3,171 children and their mothers from the Tokyo Teen Cohort (TTC) study, a population-representative longitudinal study that was launched in Tokyo in 2012. Maternal depressive/anxious symptoms and children&#x00027;s tics were examined using self-report questionnaires at the ages of 10 (time 1, T1) and 12 (time 2, T2). A cross-lagged model was used to explore the relationships between maternal depressive/anxious symptoms and children&#x00027;s tic frequency.</p>
<p><bold>Results:</bold> Higher levels of maternal depressive/anxious symptoms at T1 were related to an increased children&#x00027;s tic frequency at T2 (&#x003B2; = 0.06, <italic>p</italic> &#x0003C; 0.001). Furthermore, more frequent children&#x00027;s tics at T1 were positively related to maternal depressive/anxious symptoms at T2 (&#x003B2; = 0.06, <italic>p</italic> &#x0003C; 0.001).</p>
<p><bold>Conclusions:</bold> These findings suggest a longitudinal bidirectional relationship between maternal depressive/anxious symptoms and children&#x00027;s tic frequency in early adolescence that may exacerbate each other over time and possibly create a vicious cycle. When an early adolescent has tics, it might be important to identify and treat related maternal depressive/anxious symptoms.</p></abstract>
<kwd-group>
<kwd>tics</kwd>
<kwd>tic frequency</kwd>
<kwd>maternal depressive/anxious symptoms</kwd>
<kwd>longitudinal study</kwd>
<kwd>general population study</kwd>
<kwd>early adolescence</kwd>
</kwd-group>
<contract-num rid="cn001">JP16H06395</contract-num>
<contract-num rid="cn001">JP16H06398</contract-num>
<contract-num rid="cn001">JP16H06399</contract-num>
<contract-num rid="cn001">JP16K15566</contract-num>
<contract-num rid="cn001">JP16K21720</contract-num>
<contract-num rid="cn001">JP17H05931</contract-num>
<contract-num rid="cn001">JP19K17055</contract-num>
<contract-num rid="cn004">JP17ek0109262</contract-num>
<contract-sponsor id="cn001">Japan Society for the Promotion of Science<named-content content-type="fundref-id">10.13039/501100001691</named-content></contract-sponsor>
<contract-sponsor id="cn002">Center for Integrative Science of Human Behavior, University of Tokyo<named-content content-type="fundref-id">10.13039/501100017127</named-content></contract-sponsor>
<contract-sponsor id="cn003">International Research Center for Neurointelligence, University of Tokyo<named-content content-type="fundref-id">10.13039/501100015768</named-content></contract-sponsor>
<contract-sponsor id="cn004">Japan Agency for Medical Research and Development<named-content content-type="fundref-id">10.13039/100009619</named-content></contract-sponsor>
<counts>
<fig-count count="2"/>
<table-count count="2"/>
<equation-count count="0"/>
<ref-count count="72"/>
<page-count count="10"/>
<word-count count="7596"/>
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</article-meta>
</front>
<body>
<sec sec-type="intro" id="s1">
<title>Introduction</title>
<p>Tics are sudden, rapid, recurrent, and non-rhythmic motor movements or vocalizations. The Diagnostic and Statistical Manual of Mental Disorders, 5th edition (DSM-5) includes three tic disorders (<xref ref-type="bibr" rid="B1">1</xref>). Tourette syndrome (TS) is defined by the presence of at least two motor tic behaviors and one vocal tic behavior for a minimum period of a year, manifesting before the age of 18. Chronic tic disorder (CT) is defined by the presence of either motor or vocal tics for at least 1 year, while provisional tic disorder is defined as tics that have been present for less than a year. Recent population-based studies have demonstrated that tics are more common than previously recognized (<xref ref-type="bibr" rid="B2">2</xref>&#x02013;<xref ref-type="bibr" rid="B5">5</xref>). According to the International Classification of Diseases 10th Revision (ICD-10), which is an international diagnostic classification developed by the World Health Organization (WHO), one in five to ten children has experienced tics (<xref ref-type="bibr" rid="B6">6</xref>). Tic disorders impose a psychosocial burden on children and their families because tics are characterized by the visibility of symptoms, which can cause stigma and prejudice (<xref ref-type="bibr" rid="B7">7</xref>&#x02013;<xref ref-type="bibr" rid="B10">10</xref>). Attention-deficit/hyperactivity disorder (ADHD) and obsessive-compulsive disorder (OCD) are common comorbidities of tic disorders (<xref ref-type="bibr" rid="B7">7</xref>, <xref ref-type="bibr" rid="B11">11</xref>, <xref ref-type="bibr" rid="B12">12</xref>). Tic disorders tend to be remitted with age through adolescence (<xref ref-type="bibr" rid="B7">7</xref>, <xref ref-type="bibr" rid="B13">13</xref>, <xref ref-type="bibr" rid="B14">14</xref>). The overall similarity in these patterns of comorbidity and natural history among tic disorders suggests that tic disorders have etiological continuity (<xref ref-type="bibr" rid="B15">15</xref>&#x02013;<xref ref-type="bibr" rid="B17">17</xref>), and a recent diagnosis of &#x0201C;tic spectrum disorders&#x0201D; has been suggested (<xref ref-type="bibr" rid="B18">18</xref>). Many clinical studies and experimental studies historically use tic frequency on measures to assess severity at outcome (<xref ref-type="bibr" rid="B19">19</xref>&#x02013;<xref ref-type="bibr" rid="B24">24</xref>).</p>
<p>Tic disorders consist of a complex involvement of both multiple genes and environmental factors (<xref ref-type="bibr" rid="B25">25</xref>, <xref ref-type="bibr" rid="B26">26</xref>). Little is known about the exact brain mechanisms associated with tic development and expression (<xref ref-type="bibr" rid="B27">27</xref>, <xref ref-type="bibr" rid="B28">28</xref>), although preliminary evidence from neurochemical and neuroimaging investigations suggests a primary role for dysfunction of the dopaminergic pathways within the cortico-striato-cortico-frontal circuitry (<xref ref-type="bibr" rid="B29">29</xref>&#x02013;<xref ref-type="bibr" rid="B31">31</xref>). Environmental factors for tics include infection and autoimmune dysfunction, maternal environment during pregnancy, and psychosocial stress (<xref ref-type="bibr" rid="B11">11</xref>, <xref ref-type="bibr" rid="B28">28</xref>). It has been suggested that psychosocial factors such as trauma and intense daily psychological stress may be risk factors in individuals with genetic vulnerabilities to TS (<xref ref-type="bibr" rid="B11">11</xref>, <xref ref-type="bibr" rid="B32">32</xref>).</p>
<p>The identification of parental psychopathology could be informative in the evaluation of risk factors for the development of tic disorders in children (<xref ref-type="bibr" rid="B33">33</xref>). Previous research has shown that there is an association between maternal psychiatric symptoms and children&#x00027;s tic disorders. Chronic maternal anxious symptoms and prenatal maternal depressive symptoms have been associated with increased odds of children having TS/CT at age 13 (<xref ref-type="bibr" rid="B34">34</xref>). In another study, a maternal history of non-specific psychiatric disorders, including anxiety disorders and depressive disorders, was shown to increase odds of children having TS/CT during childhood and adolescence (<xref ref-type="bibr" rid="B35">35</xref>). It is presumed that maternal depressive/anxious symptoms are associated with the occurrence of children&#x00027;s TS/CT <italic>via</italic> maternal-specific environmental and/or genetic factors (<xref ref-type="bibr" rid="B34">34</xref>, <xref ref-type="bibr" rid="B35">35</xref>).</p>
<p>Although the association between maternal mental health and children&#x00027;s tic disorders has been proved (<xref ref-type="bibr" rid="B34">34</xref>, <xref ref-type="bibr" rid="B35">35</xref>), it is not clear whether maternal psychiatric symptoms are associated with the subsequent course of children&#x00027;s tic disorders. If maternal psychiatric symptoms predict the subsequent course of children&#x00027;s tic disorders, then maternal psychiatric symptoms could possibly be a prognostic factor or an intervention target of tic disorders. To examine this point, we investigated the relationship between maternal depressive/anxious symptoms and children&#x00027;s tic frequency in early adolescence with a longitudinal design.</p>
<p>In addition, we speculated that maternal depressive/anxious symptoms and children&#x00027;s tic frequency influence each other bidirectionally. Some studies have shown bidirectional influences on maternal and children&#x00027;s psychiatric symptoms. For example, depression in mothers increases the risk of emotional and behavioral problems in their children and vice versa (<xref ref-type="bibr" rid="B36">36</xref>, <xref ref-type="bibr" rid="B37">37</xref>). However, no study has investigated the bidirectional relationship between maternal psychiatric symptoms and children&#x00027;s tics. Research on the longitudinal bidirectional relationship between maternal depressive/anxious symptoms and children&#x00027;s tics would be helpful in advancing the research and practices related to tics.</p>
<p>Our aim was therefore to examine the relationships between maternal depressive/anxious symptoms and child&#x00027;s tic frequency in a longitudinal study design using a general population of early adolescent samples. In this population-based study, we referred to a tic or tics instead of the diagnostic term &#x0201C;tic disorders&#x0201D; because we did not make clinical diagnoses of the participants. Our hypotheses were as follows: (1) maternal depressive/anxious symptoms predict children&#x00027;s tic frequency 2 years later, and (2) maternal depressive/anxious symptoms and children&#x00027;s tic frequency influence each other bidirectionally over time.</p></sec>
<sec sec-type="materials and methods" id="s2">
<title>Materials and Methods</title>
<sec>
<title>Participants</title>
<p>This study used data from the Tokyo Teen Cohort (TTC) study (<ext-link ext-link-type="uri" xlink:href="http://ttcp.umin.jp/">http://ttcp.umin.jp/</ext-link>), a population-based longitudinal survey focusing on children&#x00027;s health from biopsychosocial multidisciplinary viewpoints (<xref ref-type="bibr" rid="B38">38</xref>). The TTC study has started from October 2012 and is currently being conducted. The participants were recruited from three municipalities in Tokyo (Setagaya, Mitaka, and Chofu) using the Basic Resident Register. The candidate participants were 14,553 children born between September 1, 2002, and August 31, 2004 (<xref ref-type="fig" rid="F1">Figure 1</xref>). Invitation letters were sent to the primary parents of those children around their 10th birthday. Of these children, 10,234 were successfully contacted, and these children were invited to participate in the cohort study. Of these 10,234 children, 4,478 children participated in the baseline survey named the Tokyo Early Adolescence Survey (T-EAS). This baseline survey was conducted from October 2012 to January 2015, when the participants were approximately 10 years old (time 1, T1). Among the 4,478 participants in the T-EAS, candidates were chosen as participants for the second wave of the TTC study. For the sake of cohort management, the target number of participants to be included in the second wave of the TTC was 3,000 children. When choosing these TTC participants, an oversampling method was used instead of inclusion criteria, considering the low follow-up rate of families with low annual household incomes. Among children who participated in T-EAS and were interested in participating in the cohort study, all 620 children whose household annual income was lower than 4,990 thousand yen were invited. From the remaining 3,858 children, 2,551 children were randomly invited to the second wave of TTC. Thus, 3,171 participants were extracted as targets for the second wave of the TTC study. The second wave of the TTC study was carried out from August 2014 to December 2016, at the time when the participants were approximately 12 years old (time 2, T2). Of the 3,171 children who were invited, 3,007 individuals participated in the second wave of the TTC study (follow-up rate 94.8%). In each wave of the data collection, trained interviewers visited the participants&#x00027; homes. They distributed questionnaires to the children and primary parents (mostly mothers), and they conducted psychological tests on the children.</p>
<fig id="F1" position="float">
<label>Figure 1</label>
<caption><p>Flowchart of participant recruitment.</p></caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fpsyt-12-767571-g0001.tif"/>
</fig></sec>
<sec>
<title>Ethical Approval</title>
<p>Ethical approval for this study was obtained from the research ethics committees of the Tokyo Metropolitan Institute of Medical Science (Approval Number: 12-35), The Graduate University for Advanced Studies, SOKENDAI (2012002), and the Graduate School of Medicine and Faculty of Medicine, The University of Tokyo (10057). We obtained informed assent from the children and written informed consent from their primary parents.</p></sec>
<sec>
<title>Measures</title>
<sec>
<title>Tic Frequency</title>
<p>We evaluated tic frequency at T1 and T2. The participants&#x00027; primary parents answered a questionnaire about the children&#x00027;s tics; this questionnaire has been used in a previous study (<xref ref-type="bibr" rid="B5">5</xref>). The questionnaire includes a section with the following five questions about specific motor and vocal tics in the past year: &#x0201C;Q1: Has your child had any repeated movements of parts of the face and head (e.g., eye blinking, grimacing, sticking tongue out, licking lips, spitting)?&#x0201D;; &#x0201C;Q2: Has your child had repeated movements of the neck, shoulder or trunk (e.g., twisting around, shoulder shrugging, bending over, nodding)?&#x0201D;; &#x0201C;Q3: Has your child had repeated movements of the arms, hands, legs, or feet?&#x0201D;; &#x0201C;Q4: Has your child had repeated noises and sounds (e.g., coughing, clearing throat, grunting, gurgling, and hissing)?&#x0201D;; and &#x0201C;Q5: Has your child had repeated words or phrases?&#x0201D; Each question is answered as either &#x0201C;definitely,&#x0201D; &#x0201C;probably,&#x0201D; or &#x0201C;not at all&#x0201D; present. Furthermore, we asked the following question about the frequency of these repetitive behaviors: &#x0201C;Q6: About how often does/did this happen in the last year?&#x0201D; This question was answered on the following 5-point Likert scale: &#x0201C;1: less than once a month, 2: 1&#x02013;3 times a month, 3: about once a week, 4: more than once a week, 5: every day.&#x0201D; We defined the participants who responded &#x0201C;definitely&#x0201D; or &#x0201C;probably&#x0201D; to any of Q1, Q2, and Q4 as having tics. The participants who only endorsed repeated movements of the arms, hands, legs or feet (Q3) or repeated words or phrases (Q5) in the absence of a positive response to the other questions about the types of tics (Q1, Q2, Q4) were excluded from a case definition to remove non-tic movements such as stereotypy or isolated echolalia. We defined as tics all responses of &#x0201C;definitely&#x0201D; or &#x0201C;probably&#x0201D; to questions concerning motor and/or vocal tics regardless of their frequency because there is no condition of frequency in the diagnostic criteria of tic disorders (<xref ref-type="bibr" rid="B1">1</xref>) and because we aimed to exhaustively find tics in the general population. For those without tics, the frequency of tics was regarded as 0, and for those with tics, the frequency of tics was evaluated on a 5-point scale from the answer in Q6.</p></sec>
<sec>
<title>Maternal Depressive/Anxious Symptoms</title>
<p>We employed the Kessler Psychological Distress Scale (K6) (<xref ref-type="bibr" rid="B39">39</xref>&#x02013;<xref ref-type="bibr" rid="B41">41</xref>) for T1 and the General Health Questionnaire-28 (GHQ-28) (<xref ref-type="bibr" rid="B42">42</xref>, <xref ref-type="bibr" rid="B43">43</xref>) for T2. The K6 and the GHQ-28 are both widely used self-report questionnaires that were developed to evaluate depressive/anxious symptoms. We used different scales between T1 and T2 in the current study because the TTC study also switched the scale used for maternal depressive/anxious symptoms from the K6 to the GHQ-28 starting at T2. The K6 is a short questionnaire consisting of 6 questions about the subjective mental distress of the respondent over the past 30 days that are answered on a 5-point scale, and the scores of the 6 items are added together (0&#x02013;24 points). The GHQ-28 consists of 28 questions about the respondent&#x00027;s subjective physical and mental states over the past few weeks, with a total score being calculated for each item by giving 0 points each for the right two responses and 1 point each for the left two responses (0&#x02013;28 points). Cutoff values are often used to screen for anxiety disorders and depression when assessing the K6 and the GHQ-28. However, in this study, we used raw values of the K6 and the GHQ-28 as continuous scales instead of screening scales, for the purpose of evaluating the severity of depressive/anxious symptoms, including the normal range in the general population. The Cronbach&#x00027;s alpha value was 0.84 for the K6 and 0.88 for the GHQ-28. We found that the distributions of the K6 and the GHQ-28 were similar based on the graphing cumulative distribution of their <italic>Z</italic> scores (<xref ref-type="supplementary-material" rid="SM1">Supplementary Figure 1</xref>). If a primary parent other than a mother answered the K6 or the GHQ-28, we regarded those responses as missing values.</p></sec>
<sec>
<title>Other Variables</title>
<p>Sex (<xref ref-type="bibr" rid="B5">5</xref>, <xref ref-type="bibr" rid="B7">7</xref>, <xref ref-type="bibr" rid="B44">44</xref>), age (<xref ref-type="bibr" rid="B32">32</xref>, <xref ref-type="bibr" rid="B45">45</xref>, <xref ref-type="bibr" rid="B46">46</xref>), maternal age (<xref ref-type="bibr" rid="B35">35</xref>, <xref ref-type="bibr" rid="B47">47</xref>&#x02013;<xref ref-type="bibr" rid="B49">49</xref>), socioeconomic status (<xref ref-type="bibr" rid="B50">50</xref>), and maternal alcohol use during pregnancy (<xref ref-type="bibr" rid="B51">51</xref>) were included in the analyses since previous studies have reported that these factors influence the occurrence of TS/CT. The data for these variables were obtained from the responses to the questionnaires completed by caregivers. To assess socioeconomic status, family income was evaluated on an 11-point scale, which ranged from &#x0201C;0&#x02013;990,000 yen&#x0201D; to &#x0201C;more than 10,000,000 yen.&#x0201D; Information on maternal alcohol use during pregnancy was obtained from maternity record books that were provided for almost all mothers by local public organizations in Japan.</p></sec></sec>
<sec>
<title>Statistical Analysis</title>
<p>Longitudinal relationships between maternal depressive/anxious symptoms and children&#x00027;s tic frequency were studied with structural equation modeling. We used SPSS&#x000AE; (Statistical Package for Social Science; IBM Corp., Armonk, N.Y. USA) version 21.0 for the characteristics of the study participants and Amos ver. 22.0 (IBM Corp, New York) for the structural equation modeling. We used the following two cross-lagged design models. The first model analyzed the longitudinal relationships between maternal depressive/anxious symptoms and children&#x00027;s tic frequency without adjusting for covariates (unadjusted model). The second model adjusted for sex, age in months, family income, maternal age, and maternal alcohol use during pregnancy (adjusted model).</p>
<p>Missing values in the categories of tics, maternal depressive/anxious symptoms, and the covariates were accounted for by full information maximum likelihood procedures available in Amos. This method estimates model parameters and standard errors using all available data while adjusting for the uncertainty associated with missing data (<xref ref-type="bibr" rid="B52">52</xref>).</p>
<p>The threshold for statistical significance was set to <italic>p</italic> &#x0003C; 0.05 (two-sided) for all analyses. We evaluated the fit of our models by using the comparative fit index (CFI) and the root mean square error of approximation (RMSEA). A good model fit was indicated by an RMSEA value smaller than 0.05 and a CFI value larger than 0.95 (<xref ref-type="bibr" rid="B53">53</xref>, <xref ref-type="bibr" rid="B54">54</xref>).</p></sec></sec>
<sec sec-type="results" id="s3">
<title>Results</title>
<sec>
<title>Characteristics of the Study Participants</title>
<p><xref ref-type="table" rid="T1">Table 1</xref> shows the demographic characteristics of the 3,171 study participants. Of the 3,171 included children, 2,601 children (82.0%) had complete data about tics across both time points; 67 (2.1%) and 484 (15.3%) children had missing data about tics in either T1 or T2, respectively, and 19 (0.6%) children had missing data about tics in both T1 and T2. Across both time points, data about maternal depressive/anxious symptoms were complete for 2,683 mothers (84.6%); 24 (0.8%) and 309 (9.7%) mothers had missing scores in either T1 or T2, respectively; and 155 mothers (4.9%) had missing data about maternal depressive/anxious symptoms in both T1 and T2.</p>
<table-wrap position="float" id="T1">
<label>Table 1</label>
<caption><p>Demographic characteristics of the participants.</p></caption>
<table frame="hsides" rules="groups">
<thead><tr>
<th valign="top" align="left"><bold>Variables</bold></th>
<th valign="top" align="center" colspan="2" style="border-bottom: thin solid #000000;"><bold>T1</bold> <bold>(10 years of age)</bold></th>
<th valign="top" align="center" colspan="2" style="border-bottom: thin solid #000000;"><bold>T2</bold> <bold>(12 years of age)</bold></th>
</tr>
<tr>
<th/>
<th valign="top" align="center"><bold>n/<italic>Mean</italic></bold></th>
<th valign="top" align="center"><bold>(%)/<italic>SD</italic></bold></th>
<th valign="top" align="center"><bold>n/<italic>Mean</italic></bold></th>
<th valign="top" align="center"><bold>(%)/<italic>SD</italic></bold></th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left">Sex, male</td>
<td valign="top" align="center">1,684</td>
<td valign="top" align="center">(53.1%)</td>
<td/>
<td/>
</tr>
<tr>
<td valign="top" align="left">Age in months</td>
<td valign="top" align="center"><italic>122.1</italic></td>
<td valign="top" align="center"><italic>3.3</italic></td>
<td valign="top" align="center"><italic>146.0</italic></td>
<td valign="top" align="center"><italic>3.7</italic></td>
</tr>
<tr>
<td valign="top" align="left">Maternal age</td>
<td valign="top" align="center"><italic>42.0</italic></td>
<td valign="top" align="center"><italic>4.2</italic></td>
<td/>
<td/>
</tr>
<tr>
<td valign="top" align="left" colspan="5">Family income<xref ref-type="table-fn" rid="TN1"><sup>a</sup></xref></td>
</tr>
<tr>
<td valign="top" align="left">&#x0003C;5 million yen</td>
<td valign="top" align="center">620</td>
<td valign="top" align="center">(20.4%)</td>
<td valign="top" align="center">448</td>
<td valign="top" align="center">(16.5%)</td>
</tr>
<tr>
<td valign="top" align="left">&#x02265;5 million yen, &#x0003C;8 million yen</td>
<td valign="top" align="center">941</td>
<td valign="top" align="center">(31.0%)</td>
<td valign="top" align="center">782</td>
<td valign="top" align="center">(28.8%)</td>
</tr>
<tr>
<td valign="top" align="left">&#x02265;8 million yen, &#x0003C;10 million yen</td>
<td valign="top" align="center">568</td>
<td valign="top" align="center">(18.6%)</td>
<td valign="top" align="center">518</td>
<td valign="top" align="center">(19.1%)</td>
</tr>
<tr>
<td valign="top" align="left">&#x02265;10 million yen</td>
<td valign="top" align="center">917</td>
<td valign="top" align="center">(30.1%)</td>
<td valign="top" align="center">970</td>
<td valign="top" align="center">(35.7%)</td>
</tr>
<tr>
<td valign="top" align="left">Maternal alcohol use during pregnancy</td>
<td valign="top" align="center">748</td>
<td valign="top" align="center">(27.2%)</td>
<td/>
<td/>
</tr>
<tr>
<td valign="top" align="left" colspan="5"><bold>Tic frequency</bold></td>
</tr>
<tr>
<td valign="top" align="left">No tics</td>
<td valign="top" align="center">2,365</td>
<td valign="top" align="center">(76.7%)</td>
<td valign="top" align="center">2,042</td>
<td valign="top" align="center">(76.5%)</td>
</tr>
<tr>
<td valign="top" align="left">With tics</td>
<td valign="top" align="center">720</td>
<td valign="top" align="center">(23.3%)</td>
<td valign="top" align="center">626</td>
<td valign="top" align="center">(23.5%)</td>
</tr>
<tr>
<td valign="top" align="left">&#x000A0;&#x000A0;&#x000A0;Less than once a month</td>
<td valign="top" align="center">138</td>
<td valign="top" align="center">(4.5%)</td>
<td valign="top" align="center">122</td>
<td valign="top" align="center">(4.6%)</td>
</tr>
<tr>
<td valign="top" align="left">&#x000A0;&#x000A0;&#x000A0;1&#x02013;3 times a month</td>
<td valign="top" align="center">114</td>
<td valign="top" align="center">(3.7%)</td>
<td valign="top" align="center">115</td>
<td valign="top" align="center">(4.3%)</td>
</tr>
<tr>
<td valign="top" align="left">&#x000A0;&#x000A0;&#x000A0;About once a week</td>
<td valign="top" align="center">37</td>
<td valign="top" align="center">(1.2%)</td>
<td valign="top" align="center">66</td>
<td valign="top" align="center">(2.5%)</td>
</tr>
<tr>
<td valign="top" align="left">&#x000A0;&#x000A0;&#x000A0;More than once a week</td>
<td valign="top" align="center">206</td>
<td valign="top" align="center">(6.7%)</td>
<td valign="top" align="center">161</td>
<td valign="top" align="center">(6.0%)</td>
</tr>
<tr>
<td valign="top" align="left">&#x000A0;&#x000A0;&#x000A0;Every day</td>
<td valign="top" align="center">225</td>
<td valign="top" align="center">(7.3%)</td>
<td valign="top" align="center">162</td>
<td valign="top" align="center">(6.1%)</td>
</tr>
<tr>
<td valign="top" align="left" colspan="5"><bold>Maternal depressive/anxious symptoms</bold></td>
</tr>
<tr>
<td valign="top" align="left">T1, K6</td>
<td valign="top" align="center"><italic>2.9</italic></td>
<td valign="top" align="center"><italic>3.3</italic></td>
<td/>
<td/>
</tr>
<tr>
<td valign="top" align="left">T2, GHQ-28</td>
<td/>
<td/>
<td valign="top" align="center"><italic>5.4</italic></td>
<td valign="top" align="center"><italic>4.9</italic></td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn id="TN1"><label>a</label><p><italic>Family income was evaluated on the 11-point scale described in section Materials and Method and categorized into the four groups in this table</italic>.</p></fn>
<p><italic>SD, standard deviation; K6, Kessler Psychological Distress Scale; GHQ-28, General Health Questionnaire-28</italic>.</p>
</table-wrap-foot>
</table-wrap>
<p>Of the participants, 23.3% children (720 of 3,085 available data) at T1 and 23.5% children (626 of 2,668 available data) at T2 had tics. These prevalence rates are consistent with previous studies that have estimated the point prevalence of tics in childhood to be approximately 20&#x02013;29% (<xref ref-type="bibr" rid="B2">2</xref>&#x02013;<xref ref-type="bibr" rid="B4">4</xref>). Of the 2,601 people whose data on the presence of tics were obtained in both T1 and T2, 332 participants endorsed tics at both T1 and T2, 280 participants endorsed tics only for T1, 265 participants endorsed tics for only T2, and 1,724 did not endorse tics at either time point.</p></sec>
<sec>
<title>Longitudinal Relationships Between Maternal Depressive/Anxious Symptoms and Children&#x00027;s Tic Frequency in Early Adolescence</title>
<p>We investigated the relationships between maternal depressive/anxious symptoms and children&#x00027;s tic frequency in a cross-lagged model analysis (<xref ref-type="fig" rid="F2">Figure 2</xref>, <xref ref-type="table" rid="T2">Table 2</xref>). There was a cross-sectional association between maternal depressive/anxious symptoms and child&#x00027;s tic frequency at T1 and T2. Higher levels of maternal depressive/anxious symptoms at T1 significantly increased children&#x00027;s tic frequency at T2 (adjusted model: &#x003B2; = 0.06, <italic>p</italic> &#x0003C; 0.001). In contrast, higher frequency of children&#x00027;s tics at T1 was related to higher levels of maternal depressive/anxious symptoms at T2 (adjusted model: &#x003B2; = 0.06, <italic>p</italic> &#x0003C; 0.001). All of these models indicated good model fit to the data (adjusted model: CFI = 0.950, RMSEA = 0.046). These results revealed that maternal depressive/anxious symptoms and children&#x00027;s tic frequency had longitudinal, bidirectional relationships with each other.</p>
<fig id="F2" position="float">
<label>Figure 2</label>
<caption><p>Cross-lagged model of relationships between maternal depressive/anxious symptoms and children&#x00027;s tic frequency. This figure shows the results of the adjusted model in <xref ref-type="table" rid="T2">Table 2</xref>. Paths from covariates are omitted from the figure. e, error variable; T1, 10 years of age; T2, 12 years of age. &#x0002A;&#x0002A;&#x0002A;<italic>p</italic> &#x0003C; 0.001.</p></caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fpsyt-12-767571-g0002.tif"/>
</fig>
<table-wrap position="float" id="T2">
<label>Table 2</label>
<caption><p>Relationships between maternal depressive/anxious symptoms and children&#x00027;s tic frequency (n = 3,171).</p></caption>
<table frame="hsides" rules="groups">
<thead><tr>
<th/>
<th valign="top" align="center" colspan="5" style="border-bottom: thin solid #000000;"><bold>Unadjusted model</bold></th>
<th valign="top" align="center" colspan="5" style="border-bottom: thin solid #000000;"><bold>Adjusted model</bold></th>
</tr>
<tr>
<th valign="top" align="left"><bold>Path</bold></th>
<th valign="top" align="center"><bold>&#x003B2;</bold></th>
<th valign="top" align="center"><bold>B</bold></th>
<th valign="top" align="center"><bold>SE</bold></th>
<th valign="top" align="center"><bold>95% CI</bold></th>
<th valign="top" align="center"><bold><italic>p-</italic>value</bold></th>
<th valign="top" align="center"><bold>&#x003B2;</bold></th>
<th valign="top" align="center"><bold>B</bold></th>
<th valign="top" align="center"><bold>SE</bold></th>
<th valign="top" align="center"><bold>95% CI</bold></th>
<th valign="top" align="center"><bold><italic>p-</italic>value</bold></th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left">Maternal depressive/anxious symptoms T1 &#x021D4;<break/> Children&#x00027;s tic frequency T1</td>
<td valign="top" align="center">0.10</td>
<td valign="top" align="center">0.50</td>
<td valign="top" align="center">0.10</td>
<td valign="top" align="center">0.31&#x02013;0.70</td>
<td valign="top" align="center">&#x0003C;0.001</td>
<td valign="top" align="center">0.09</td>
<td valign="top" align="center">0.49</td>
<td valign="top" align="center">0.10</td>
<td valign="top" align="center">0.30&#x02013;0.69</td>
<td valign="top" align="center">&#x0003C;0.001</td>
</tr>
<tr>
<td valign="top" align="left">Maternal depressive/anxious symptoms T2 &#x021D4;<break/> Children&#x00027;s tic frequency T2</td>
<td valign="top" align="center">0.09</td>
<td valign="top" align="center">0.52</td>
<td valign="top" align="center">0.12</td>
<td valign="top" align="center">0.28&#x02013;0.75</td>
<td valign="top" align="center">&#x0003C;0.001</td>
<td valign="top" align="center">0.08</td>
<td valign="top" align="center">0.50</td>
<td valign="top" align="center">0.12</td>
<td valign="top" align="center">0.26&#x02013;0.73</td>
<td valign="top" align="center">&#x0003C;0.001</td>
</tr>
<tr>
<td valign="top" align="left">Maternal depressive/anxious symptoms T1 &#x02192; <break/> Maternal depressive/anxious symptoms T2</td>
<td valign="top" align="center">0.47</td>
<td valign="top" align="center">0.69</td>
<td valign="top" align="center">0.03</td>
<td valign="top" align="center">0.09&#x02013;0.74</td>
<td valign="top" align="center">&#x0003C;0.001</td>
<td valign="top" align="center">0.46</td>
<td valign="top" align="center">0.68</td>
<td valign="top" align="center">0.03</td>
<td valign="top" align="center">0.63&#x02013;0.73</td>
<td valign="top" align="center">&#x0003C;0.001</td>
</tr>
<tr>
<td valign="top" align="left">Children&#x00027;s tic frequency t1 &#x02192; <break/> Children&#x00027;s tic frequency T2</td>
<td valign="top" align="center">0.41</td>
<td valign="top" align="center">0.39</td>
<td valign="top" align="center">0.02</td>
<td valign="top" align="center">0.35&#x02013;0.42</td>
<td valign="top" align="center">&#x0003C;0.001</td>
<td valign="top" align="center">0.40</td>
<td valign="top" align="center">0.38</td>
<td valign="top" align="center">0.02</td>
<td valign="top" align="center">0.35&#x02013;0.41</td>
<td valign="top" align="center">&#x0003C;0.001</td>
</tr>
<tr>
<td valign="top" align="left">Maternal depressive/anxious symptoms T1 &#x02192; <break/> Children&#x00027;s tic frequency T2</td>
<td valign="top" align="center">0.06</td>
<td valign="top" align="center">0.03</td>
<td valign="top" align="center">0.01</td>
<td valign="top" align="center">0.01&#x02013;0.05</td>
<td valign="top" align="center">&#x0003C;0.001</td>
<td valign="top" align="center">0.06</td>
<td valign="top" align="center">0.03</td>
<td valign="top" align="center">0.01</td>
<td valign="top" align="center">0.01&#x02013;0.04</td>
<td valign="top" align="center">&#x0003C;0.001</td>
</tr>
<tr>
<td valign="top" align="left">Children&#x00027;s tic frequency T1 &#x02192; <break/> Maternal depressive/anxious symptoms T2</td>
<td valign="top" align="center">0.07</td>
<td valign="top" align="center">0.20</td>
<td valign="top" align="center">0.05</td>
<td valign="top" align="center">0.10&#x02013;0.30</td>
<td valign="top" align="center">&#x0003C;0.001</td>
<td valign="top" align="center">0.06</td>
<td valign="top" align="center">0.19</td>
<td valign="top" align="center">0.05</td>
<td valign="top" align="center">0.09&#x02013;0.30</td>
<td valign="top" align="center">&#x0003C;0.001</td>
</tr> <tr style="border-top: thin solid #000000;">
<td/>
<td valign="top" align="center" colspan="5">&#x003C7;<sup>2</sup> = 0, Degrees of freedom = 0, <italic>p</italic> = -, CFI = 1.0, RMSEA = 0 (saturated model)</td>
<td valign="top" align="center" colspan="5">&#x003C7;<sup>2</sup> = 77.834, Degrees of freedom = 10, <italic>p</italic> &#x0003C; 0.001, CFI = 0.950, RMSEA = 0.046</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p><italic>T1, 10 years of age; T2, 12 years of age; &#x003B2;, standardized coefficient; B, coefficient; SE, standard error; CI, confidence interval; CFI, comparative fit index; RMSEA, root mean square error of approximation</italic>.</p>
</table-wrap-foot>
</table-wrap>
</sec></sec>
<sec sec-type="discussion" id="s4">
<title>Discussion</title>
<p>This was the first study to examine the longitudinal relationships between maternal depressive/anxious symptoms and children&#x00027;s tic frequency in a population-based early adolescent sample. The following two findings were obtained. First, when more severe maternal depressive/anxious symptoms are present, children are likely to present more frequent tics 2 years later. Second, the severity of maternal depressive/anxious symptoms and children&#x00027;s tic frequency are longitudinally associated with each other.</p>
<p>The present results showed cross-sectional relationship between maternal anxiety/depressive symptoms and children&#x00027;s tic frequency and small but significant longitudinal bidirectional relationship between them. Previous studies showed relationship between past maternal mental symptoms and children&#x00027;s TS/CT, and presumed that maternal mental symptoms are associated with the occurrence of children&#x00027;s TS/CT <italic>via</italic> maternal-specific environmental and/or genetic factors (<xref ref-type="bibr" rid="B34">34</xref>, <xref ref-type="bibr" rid="B35">35</xref>). The present results is consistent with those previous studies and provided a new perspective that suggests longitudinal bidirectional relationship between maternal anxiety/depressive symptoms and children&#x00027;s tic frequency.</p>
<p>Several explanations may be possible for the significant magnitude-response relationship between maternal depressive/anxious symptoms and children&#x00027;s later tic frequency. First, maternal depressive/anxious symptoms may affect the occurrence, persistence, and exacerbation of children&#x00027;s tics as an environmental factor because environmental factors such as psychosocial stresses are known to exacerbate tics (<xref ref-type="bibr" rid="B55">55</xref>&#x02013;<xref ref-type="bibr" rid="B59">59</xref>). In addition, several studies have shown that tic frequency can be influenced by antecedent environmental events and social consequences although they referred relatively immediate and short term reaction. For example, some activities reduce tic frequency such as focusing attention away from tics (<xref ref-type="bibr" rid="B60">60</xref>), aerobic exercise training (<xref ref-type="bibr" rid="B61">61</xref>) and participation in musical activity (<xref ref-type="bibr" rid="B62">62</xref>). There are no reports of an association between maternal psychiatric symptoms and the course of children&#x00027;s tics. However, some studies have shown an association between maternal psychiatric symptoms and the course of children&#x00027;s psychiatric symptoms. For example, maternal depression has been shown to be associated with increased psychiatric diagnoses and emotional and behavioral problems in children, and when maternal depression is remitted, the children&#x00027;s problems are more likely to also be in remission (<xref ref-type="bibr" rid="B63">63</xref>). Furthermore, improvement in parental depression has a positive impact on the health, emotional, cognitive, academic and overall functioning of children (<xref ref-type="bibr" rid="B64">64</xref>). Thus, similar to these reports, maternal depressive/anxious symptoms might affect the course of children&#x00027;s tics as an environmental factor. Second, there might be genetic relationships between maternal depressive/anxious symptoms and the occurrence, persistence, and exacerbation of tics. Family studies of TS have suggested that TS has genetic correlations with depressive disorders and anxiety disorders (<xref ref-type="bibr" rid="B65">65</xref>, <xref ref-type="bibr" rid="B66">66</xref>), although these correlations are possibly mediated through ADHD and OCD (<xref ref-type="bibr" rid="B66">66</xref>). There has been no research examining the genetic relationships between maternal depressive/anxious symptoms and the persistence or exacerbation of tics, but the results of this research could not rule out these possibilities. Furthermore, there is also a possibility that an interaction of genetic and environmental factors is involved in the relationships between maternal depressive/anxious symptoms and children&#x00027;s tics. The results of this study could not distinguish genetic and environmental contributors to the relationships between maternal depressive/anxious symptoms and children&#x00027;s tics.</p>
<p>Our findings on the association between children&#x00027;s tic frequency and increased maternal depressive/anxious symptoms 2 years later can be explained by several potential mechanisms. One of the possible mechanisms is that the parenting stress associated with bringing up children with tics might influence maternal depressive/anxious symptoms. Parents of children with TS experience increased levels of caregiver burdens and parenting stress compared to parents of children without TS (<xref ref-type="bibr" rid="B67">67</xref>, <xref ref-type="bibr" rid="B68">68</xref>). The visible nature of tics can have an impact on the parent-child relationship, with parents becoming overprotective of, worrying about, struggling to accept or trying to control children&#x00027;s tics, which can lead to family conflicts, poor parent-child relationships and increased frustrations in parenting (<xref ref-type="bibr" rid="B7">7</xref>, <xref ref-type="bibr" rid="B9">9</xref>, <xref ref-type="bibr" rid="B10">10</xref>, <xref ref-type="bibr" rid="B69">69</xref>, <xref ref-type="bibr" rid="B70">70</xref>). Parenting stress in parents of children with tics could also occur due to children&#x00027;s comorbidities, such as ADHD, OCD, and behavioral problems (<xref ref-type="bibr" rid="B67">67</xref>, <xref ref-type="bibr" rid="B68">68</xref>). In a previous population-based study, 21.2% of children had tics, and children with tics were more affected by psychopathologies, including ADHD and OCD, than were children without tics (<xref ref-type="bibr" rid="B12">12</xref>). In addition to these environmental factors, both genetic factors and genetic/environmental interactions might have an effect of children&#x00027;s tics on maternal depressive/anxious symptoms.</p>
<p>The implications of this study were that the longitudinal bidirectional relationships between maternal depressive/anxious symptoms and children&#x00027;s tic frequency may suggest a vicious cycle in which maternal depressive/anxious symptoms make tic frequency increased, and children&#x00027;s tic frequency make maternal depressive/anxious symptoms worse. This study also suggested that not only intervention in children&#x00027;s tics but also intervention in maternal depressive/anxious symptoms might be important for the treatment of tics. However, the present study was unable to separate genetic and environmental factors in the association between children&#x00027;s tic frequency and maternal depressive/anxious symptoms; therefore, further research is needed to determine the effect of intervention on maternal anxiety/depressive symptoms. While there has been a consensus on the importance of family psychoeducation in the treatment of tics (<xref ref-type="bibr" rid="B7">7</xref>, <xref ref-type="bibr" rid="B27">27</xref>), it is not known whether maternal psychiatric problems influence the course of children&#x00027;s tics. This study provides new insights for future research and practice.</p>
<p>The strength of this study was that, for the first time, it was shown that higher levels of maternal depressive/anxious symptoms are related to an increased children&#x00027;s tic frequency 2 years later and that there are longitudinal relationships between maternal depressive/anxious symptoms and children&#x00027;s tic frequency. Other strengths were the large sample size, the high follow-up rate of the study, and the inclusion of non-clinical tics. In contrast, this study also had several limitations. First, we used different measures of maternal depressive/anxious symptoms for T1 and T2. We found that the distributions of the K6 and the GHQ-28 were similar by graphing the cumulative distribution of the <italic>Z</italic> scores of the K6 and the GHQ-28 (<xref ref-type="supplementary-material" rid="SM1">Supplementary Figure 1</xref>). Additionally, this limitation did not influence the course from maternal depressive/anxious symptoms to children&#x00027;s tic frequency. Second, in this study, children&#x00027;s tics were evaluated not by direct clinical assessments but by questionnaires to caregivers. However, we deliberately chose rigorous tic definitions and sought to exclude participants with non-tic movement disorders (e.g., stereotypies associated with autism or an intellectual disability, repetitive arm/leg movements that could be better explained by tremor, or motor restlessness) (<xref ref-type="bibr" rid="B5">5</xref>). In this study, the prevalence of tics was 23.3% at age 10 and 23.5% at age 12. These prevalence rates could be considered reasonable based on the following evidence. Point prevalence depends strongly on age; the highest rate is estimated to be approximately 20% at age 5&#x02013;10, and the lifetime prevalence is much higher (<xref ref-type="bibr" rid="B3">3</xref>). In previous studies that have directly observed children, tics were found in 29.2% of fourth-grade children in an elementary school in Washington D.C. (<xref ref-type="bibr" rid="B2">2</xref>) and in 21.2% of children aged 9&#x02013;17 years old (mean 13.1 years old) in Monroe County, Rochester, New York (<xref ref-type="bibr" rid="B4">4</xref>). The prevalence rates of tics in the present study were consistent with those found in these previous studies. Third, the data analysis in this study could not adjust for ADHD and OCD, which are frequently comorbid with tics. That may be because of the strong association of tics with ADHD and OCD. Future studies are needed to examine the effects of ADHD and OCD on the bidirectional relationships between maternal depressive/anxious symptoms and children&#x00027;s tic frequency. The fourth limitation was that the research interval in this longitudinal study was relatively short. Typically, tics improve gradually during adolescence, with repeated periods of remission and exacerbation. Thus, it might be difficult to capture change in the short research period of 2 years. Longer-term follow-up periods are needed in the future. The fifth limitation was that we did not collect information about the maternal history of tics. Given the low rate of medical consultation for tics (<xref ref-type="bibr" rid="B5">5</xref>, <xref ref-type="bibr" rid="B12">12</xref>, <xref ref-type="bibr" rid="B65">65</xref>) and the clinical outcome that tics often improve or disappear after adolescence (<xref ref-type="bibr" rid="B7">7</xref>, <xref ref-type="bibr" rid="B13">13</xref>, <xref ref-type="bibr" rid="B14">14</xref>), it is probably not possible to obtain accurate information on the maternal history of tics. Finally, there were also some limitations inherent to the cross-lagged model (<xref ref-type="bibr" rid="B71">71</xref>); i.e., there is a possibility that there are multiple potential additional factors (not included in the model) that influence the bidirectional relationship over time.</p>
<p>The following two studies would be helpful in testing the viability of the relationships between maternal depressive/anxious symptoms and children&#x00027;s tic frequency and in advancing research and practice. First, if the course of children&#x00027;s tic frequency could be observed at three or more time points, it would be possible to confirm the vicious cycle that develops between maternal depressive/anxious symptoms and children&#x00027;s tics and to investigate the mediating factors. For example, children&#x00027;s anxiety/depression symptoms might mediate the relationships between maternal depressive/anxious symptoms and children&#x00027;s tic frequency. In addition, comorbidities or poor quality of life might mediate the relationships between children&#x00027;s tic frequency and maternal depressive/anxious symptoms. Second, intervention studies could examine whether improvements in maternal depressive/anxious symptoms improve children&#x00027;s tics.</p>
<p>This study was the first to show the relationship between preceding maternal depressive/anxious symptoms and an increased children&#x00027;s tic frequency 2 years later in early adolescence. Furthermore, we found longitudinal bidirectional relationships between maternal depressive/anxious symptoms and children&#x00027;s tic frequency. Although we could not separate environmental factors and genetic factors in this research, the findings implied that it may be important to care not only for children with tics but also for their mothers&#x00027; depressive/anxious symptoms when tics are treated in early adolescence.</p></sec>
<sec sec-type="data-availability" id="s5">
<title>Data Availability Statement</title>
<p>The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.</p></sec>
<sec id="s6">
<title>Ethics Statement</title>
<p>The studies involving human participants were reviewed and approved by the Tokyo Metropolitan Institute of Medical Science (Approval Number: 12-35), the Graduate University for Advanced Studies, SOKENDAI (2012002), the Graduate School of Medicine and Faculty of Medicine, the University of Tokyo (10057). Written informed consent to participate in this study was provided by the participants&#x00027; legal guardian/next of kin.</p></sec>
<sec id="s7">
<title>Author Contributions</title>
<p>TY conceptualized and designed the study, drafted the initial manuscript, reviewed and revised the manuscript, and being supervised by SA. AN, SY, YK, and KK critically reviewed the manuscript for important intellectual content and contributed to the discussion. SU supervised the statistical analysis. All authors contributed to and have approved the final manuscript.</p></sec>
<sec sec-type="funding-information" id="s8">
<title>Funding</title>
<p>This work was supported by Grant-in-Aid for Scientific Research on Innovative Areas (JP23118002 and JP16H01689; Adolescent Mind and Self-Regulation) from the Ministry of Education, Culture, Sports, Science, and Technology of Japan. This study was also supported in part by JSPS KAKENHI Grant Numbers JP16H06395, JP16H06398, JP16H06399, JP16K15566, JP16K21720, JP17H05931, and JP19K17055, by UTokyo Center for Integrative Science of Human Behavior (CiSHuB), by the International Research Center for Neurointelligence (WPI-IRCN) at the University of Tokyo Institutes for Advanced Study (UTIAS), and by AMED under Grant Number JP17ek0109262. The funding source had no role in the preparation, review, or approval of the manuscript, and the decision to submit the manuscript for publication.</p>
</sec>
<sec sec-type="COI-statement" id="conf1">
<title>Conflict of Interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p></sec>
<sec sec-type="disclaimer" id="s9">
<title>Publisher&#x00027;s Note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p></sec> </body>
<back>
<ack><p>The authors would like to gratefully acknowledge the collaboration of all participants in this study. This manuscript has been previously published as a preprint in Research Square (<xref ref-type="bibr" rid="B72">72</xref>).</p>
</ack>
<sec sec-type="supplementary-material" id="s10">
<title>Supplementary Material</title>
<p>The Supplementary Material for this article can be found online at: <ext-link ext-link-type="uri" xlink:href="https://www.frontiersin.org/articles/10.3389/fpsyt.2021.767571/full#supplementary-material">https://www.frontiersin.org/articles/10.3389/fpsyt.2021.767571/full#supplementary-material</ext-link></p>
<supplementary-material xlink:href="Image_1.jpg" id="SM1" mimetype="image/jpeg" xmlns:xlink="http://www.w3.org/1999/xlink"/></sec>
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<glossary>
<def-list>
<title>Abbreviations</title>
<def-item><term>ADHD</term>
<def><p>attention-deficit/hyperactivity disorder</p></def></def-item>
<def-item><term>CFI</term>
<def><p>comparative fit index</p></def></def-item>
<def-item><term>CI</term>
<def><p>confidence interval</p></def></def-item>
<def-item><term>CT</term>
<def><p>chronic tic disorder</p></def></def-item>
<def-item><term>DSM-5</term>
<def><p>Diagnostic and Statistical Manual of Mental Disorders 5th edition</p></def></def-item>
<def-item><term>GHQ-28</term>
<def><p>General Health Questionnaire-28</p></def></def-item>
<def-item><term>K6</term>
<def><p>Kessler Psychological Distress Scale</p></def></def-item>
<def-item><term>OCD</term>
<def><p>obsessive-compulsive disorder</p></def></def-item>
<def-item><term>RMSEA</term>
<def><p>root mean square error of approximation</p></def></def-item>
<def-item><term>SD</term>
<def><p>standard deviation</p></def></def-item>
<def-item><term>TS</term>
<def><p>Tourette syndrome</p></def></def-item>
<def-item><term>TTC</term>
<def><p>Tokyo Teen Cohort.</p></def></def-item>
</def-list>
</glossary> 
</back>
</article> 