ORIGINAL RESEARCH article

Front. Aging Neurosci., 31 March 2022

Sec. Neurocognitive Aging and Behavior

Volume 14 - 2022 | https://doi.org/10.3389/fnagi.2022.789190

Functional Cognitive Disorder Presents High Frequency and Distinct Clinical Profile in Patients With Low Education

  • 1. Cognitive and Behavioral Neurology Center, Serviço de Neurologia, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil

  • 2. Graduate Program in Biological Sciences: Pharmacology and Therapeutics, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil

  • 3. Graduate Program in Biological Sciences: Biochemistry, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil

  • 4. Departamento de Farmacologia, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil

Abstract

Introduction:

Functional Cognitive Disorder (FCD) is a non-degenerative, common cause of memory complaint in patients with high educational levels. FCD has been insufficiently described in individuals with low education. Here, we investigated the frequency of FCD among individuals with low education.

Methods:

We analyzed retrospectively all new referrals from primary care to a tertiary memory clinic from 2014 to 2021. Final diagnosis, diagnostic work-up, clinical and cognitive testing data were compared between FCD and other diagnoses, grouped as Neurodegenerative Disorders (NDD). A regression model was used to assess the effect of education on the diagnosis. Data is shown in Mean [SD].

Results:

A total of 516 individuals (70.76 [10.3] years) with low educational attainment (4.5 [3.94] years) were divided into FCD (146, 28.3%) and NDD. Compared with NDD, FCD patients showed lower age at presentation (66.2 [9.4] vs. 72.6 [10.2], p < 0.001), higher Mini-Mental State Examination (MMSE) scores (22.4 [6.2] vs. 14.7 [7.8], p < 0.001) and Geriatric Depression Scale (GDS) scores (7.4 [5.4] vs. 5.3 [3.7], p = 0.0001).

Discussion:

Surprisingly, FCD was the most frequent diagnosis in a low educational setting. However, education was not associated with FCD. Individuals presenting FCD showed a distinct clinical profile, including younger age and higher depressive scores. Strategies to identify FCD in primary care settings may benefit both patients and healthcare systems.

Introduction

Functional cognitive disorder (FCD) is within the umbrella-term “functional neurological disorders.” It indicates the presence of a cognitive complaint not caused by a systemic or brain disease (; ). FCD is a poor predictor of progressive cognitive impairment, and only a minority of individuals with FCD evolve to dementia (). However, this clinical entity is prevalent in memory clinics worldwide (), and it may exhibit different clinical characteristics.

A variety of neurological presentations have been described in patients with FCD. Cognitive complaints, especially memory, are commonly presented by patients with FCD, though not confirmed objectively. This inconsistency between the cognitive evaluation and the clinical interview is a strong indicator of a functional disorder (). By definition, individuals with FCD exhibit cognitive complaints in the absence of detectable cognitive decline, while individuals with Mild Cognitive Impairment (MCI) phenotypically manifest objective impairment. Patients with FCD typically present to the consultation presenting with symptoms of depression or anxiety (). Subjective memory complaints were also often described by these patients (), which is a prevalent clinical entity in memory clinics worldwide. Paradoxically, affective disorders associated with cognitive complaints may be both the etiology and a strong predictor of further cognitive decline (; ). Finally, the complex relationship between psychological distress and neuropathological changes is somewhat controversial.

Studies of the epidemiology of FCD found substantially variable results. Overlapping definitions, heterogeneous diagnostic criteria, and diverse methodology to classify these individuals are sources of variability for measuring its prevalence (). Previous studies suggest that FCD prevalence ranges from 10% to over 50% of diagnoses in different clinical settings (; ; ; ). Most of these studies were conducted in high-income countries, especially with higher levels of education, which does not correspond to the majority of patients living with dementia (). Educational attainment is an important proxy of cognitive reserve, and it plays a significant influence on the pathophysiology of cognitive decline (). An individual’s level of education has also been described as a long-term protective factor for anxiety and depression (; ). However, whether education and FCD are associated remains unclear. Herein, we aimed at identifying the frequency of FCD in a Brazilian tertiary memory clinic with a low education patient profile.

Materials and Methods

Study Design

A retrospective analysis was conducted with all new referrals to our tertiary memory clinic from January, 2014 to January, 2021. Individuals were referred by a general practitioner or family physician from the primary care setting of the Brazilian public health system (SUS, Sistema Único de Saúde). All patients that attended the memory clinic as a primary consultation were included in this study. This study was approved by the institution Ethics Committee under the IRB number 4.645.978.

Data Collection

Patients underwent a routine evaluation comprising a semi-structured interview, cognitive screening evaluation, neurological examination, neuropsychological evaluation according to clinical indication, a neuroimaging exam (either a CT or MRI), and laboratory screening for potentially reversible causes of dementia (syphilis, HIV, B and C hepatitis serology, B12, folate, thyrotropin, creatinine, electrolytes levels, and total blood count). Then, they were classified into dementia syndromes according to the international diagnostic criteria as follows: MCI(), Alzheimer’s disease dementia (AD; ), vascular dementia (VD; ), mixed dementia (AD and VD), and other less prevalent conditions [frontotemporal dementia (FTD; ), Lewy bodies dementia, corticobasal syndrome, among others] (). Individuals with advanced stages of dementia, with indistinguishable clinical characteristics at disease onset, were classified as “Unspecified.” In order to distinguish and characterize FCD from other diagnoses, individuals with a diagnosis of any type of dementia were included in the Neurodegenerative Disorder group (NDD).

Functional Cognitive Disorder was defined according to previously published criteria (), as follows: (1) one or more symptoms of cognitive impairment; (2) clinical evidence of internal inconsistency (discrepancy between a complaint and clinical judgment); (3) symptoms of impairment not explained by another medical condition; and (4) symptoms cause clinically substantial distress or impairment in social, occupational, or other important areas of function, or warrant medical evaluation. Individuals diagnosed with subjective cognitive decline were also included as FCD (). Importantly, FCD is a clinical entity that suggests a psychological/functional basis of cognitive complaint or even cognitive decline.

Outcome Measures

Electronic records of all patients were evaluated for the following demographic and cognitive variables: date of appointment, age, sex, education, use of any substance (alcohol, tobacco, illicit drugs), previous and current pathologies, medication in use, the Mini-Mental State Examination (MMSE; ), the Geriatric Depression Scale–15 item version (GDS; ), and the Functional Activities Questionnaire (FAQ; ).

Statistical Analysis

Frequencies and categorical variables were compared with Chi-squared tests. A logistic regression model was performed using age, education, and total MMSE scores as predictors of NDD. When appropriate, group comparisons between FCD, MCI, and NDD individuals were performed using analysis of variance with Tukey’s post-hoc test, and chi-square tests. We performed Bonferroni’s correction for multiple comparisons and p-values were considered significant at <0.05. Continuous variables were defined as mean ± standard deviation. Data analysis was performed using R 3.6.2 (R foundation for statistical computing, 2016), and variables with missing values above 9% were excluded. Comorbidities that were not described in the records were considered absent, or not diagnosed yet. Missing data are exhibited in the Supplementary Table 1.

Results

Five hundred and sixteen (516) patients (mean age 70.76 ± 10.3 years, 61% females) were referred to the memory clinic from January 2014 to January 2021. The whole sample presented an average of 4.5 (± 3.94) years of education, including 71 (13.75%) illiterates, and mean MMSE score was 14.42 (± 8.17). Clinical comorbidities and use of substances are described in Table 1. Males presented increased alcohol use (Supplementary Table 3, p < 0.001).

TABLE 1

Functional cognitive disorder (n = 146)Mild cognitive impairment (n = 51)Neurodegenerative disorders (n = 299)Corrected p-value
Age, mean (SD)66.2 (± 9.4)73.7 (± 8.4)72.4 (± 10.4)<0.0001
Sex (F)100 (68.5%)29 (56.9%)174 (58.2%)0.87
Education, mean (SD)5.6 (± 3.9)5.3 (± 3.9)4.9 (± 4.0)0.17
Mini-mental state examination, mean (SD)22.4 (± 6.2)21.4 (± 4.4)13.6 (± 7.6)<0.0001
Geriatric depression scale–15 item, mean (SD)7.4 (± 4.5)3.5 (± 3.0)5.7 (± 3.7)<0.0001
Functional assessment questionnaire, mean (SD)6.9 (± 7.6)6.2 (± 5.7)20.2 (± 8.4)<0.0001
Substance use, n (%)
Active smoking13 (8.9%)6 (11.8%)22 (7.4%)0.82
Active alcohol drinking5 (3.4%)3 (5.9%)12 (4.0%)0.55
Comorbidities, n (%)
Hypertension83 (56.8%)34 (66.7%)187 (62.5%)0.37
Diabetes33 (22.6%)17 (33.3%)83 (27.8%)0.26
Dyslipidemia31 (21.2%)20 (39.2%)75 (25.1%)0.04
Malignancy7 (4.8%)3 (5.9%)22 (7.4%)0.65
Heart failure5 (3.4%)010 (2.9%)0.57
Hypothyroidism14 (9.6%)5 (9.8%)23 (7.7%)0.69
Major depression25 (17.1%)3 (5.9%)16 (5.4%)<0.0001
Medications, n (%)
Anti-hypertensive drug79 (54.5%)32 (62.7%)170 (57.0%)0.6
Antidepressant drug69 (47.6%)14 (27.5%)106 (35.6%)0.01
Antipsychotic drug33 (22.8%)3 (5.9%)85 (28.5%)0.0007
Acetylcholinesterase inhibitor5 (3.4%)4 (7.8%)58 (39.7%)<0.001
Benzodiazepines20 (13.8%)5 (9.8%)34 (11.4%)0.8

Demographic and clinical characteristics of patients that attended the memory clinic within the period of 2014–2021.

FCD, functional cognitive disorder; MCI, mild cognitive impairment; NDD, neurodegenerative disorders. Bold represents statistically significant p-values.

Functional cognitive disorder (146, 28.3%) was the most common diagnosis, followed by AD dementia (115, 22.3%), MCI (51, 9.9%), VD (36, 7%) and mixed-type dementia (25, 4.9%) (Figure 1). Other less common diagnoses included behavioral variant FTD (5, 0.9%), Lewy bodies dementia (4, 0.7%), unspecified dementia (72, 13.9%) and others (42, 8.6%). Patients under investigation (19, 3.7%) were not included in this analysis.

FIGURE 1

Ninety-three patients with FCD (63.7%) were diagnosed with a psychiatric disorder, namely major depressive disorder, anxiety or bipolar disorder, and 53 (36.3%) with Subjective Cognitive Decline. FCD accounted for an annual average of 16.79% of all referrals in this period, varying from 9.1% (2020, n = 1/11) to 38.84% (2014, n = 23/66) (Figure 2). Compared with NDD, patients with FCD presented higher MMSE and GDS and lower age and FAQ (Table 1). MCI also exhibited distinct characteristics when compared with FCD (Table 1). Though they presented similar MMSE scores, MCI was significantly older than FCD individuals, and had less depressive symptoms (p < 0.0001 for both).

FIGURE 2

Females presenting NDD were older and exhibited a higher frequency of major depression than males presenting NDD (Supplementary Table 3, p = 0.03 and p < 0.0001, respectively). Duration of symptoms, history of hypertension, diabetes, hypercholesterolemia and heart failure were similar between groups (p > 0.05), but the frequency of major depression was higher in FCD (p < 0.001). Cardiovascular and clinical comorbidities risk factors were similar between groups. It is also important to mention that five (5) FCD individuals were receiving an acetylcholinesterase inhibitor. In a logistic regression model, including age, education, and total MMSE, only age (p < 0.001) and total MMSE scores (p < 0.001) were predictors of FCD diagnosis (Table 2). The FAQ and GDS scores were not included in the regression analysis.

TABLE 2

VariableEstimatez-valuep-valueOR (95% CI)
Age0.050.010.0061.06 (1.03–1.08)
Education0.090.03<0.0011.09 (1.02–1.17)
MMSE scores−0.160.02<0.0010.84 (0.8–0.88)

Logistic regression model using diagnosis of neurodegenerative disorder as outcome.

Discussion

Functional cognitive Disorder was the most frequent diagnosis among patients with low education, even more frequent than Alzheimer’s disease. Our sample consisted of individuals directly referred from primary care within the public health system, which represents the majority of individuals nationally. Although education was not a predictor of FCD, patients presenting FCD showed a distinct profile of clinical presentation.

Patients with low educational attainment are under-represented in studies of neurodegenerative diseases worldwide, even though most patients with dementia live in low and middle-income countries (). High level of education is a proxy of cognitive reserve, and it should be considered in studies of dementia and cognitive decline (). Our findings indicate that FCD is also common in a low educational setting. The frequency we found was similar to observed in studies conducted in contexts with a higher level of education, which ranged from a quarter () to a half of patients consulting in a tertiary memory clinic (). A complex range of reasons may be associated with this similarity. The contrast between cognitive evaluation and the clinical complaint is a hallmark of FCD, which is possibly not associated with brain areas connected to education or cognitive reserve (). Moreover, primary care physicians from high and low educational settings may share similar doubts in diagnosing dementia. Besides, psychological distress is widely spread, but highly underdiagnosed in both settings (; ).

In fact, distinguishing FCD from cognitive symptoms of NDDs is challenging. Cell senescence has been increasingly associated with pathological brain aging, as its biological mechanisms may play a central role in elucidating the aging process and neuroinflammatory response (). Astrocytic and microglial senescence has been linked to age-associated inflammation and decreased neuroprotection (). Cognitive reserve, here proxied by education, has been described as a major neuroprotective factor during brain aging, but its underlying mechanisms are widely unclear. Low education may possibly reflect increased cell senescence process and early cognitive impairment due to many mechanisms (). It is hypothesized that education may interact with glial cells that assume protective states in individuals with higher reserve. Besides, inflammaging is a well described phenomenon () involving astrocyte senescence, microglial dystrophy () and ultimately neuronal integrity (). Plastic cell responses to brain pathology may involve dendritic pruning (), but also astrocytes exhibit detrimental processes in synaptic transmission in cognitive aging (). Astrocytes may particularly contribute to neuroprotection, both stabilizing synapses and improving cell survival (). Elucidating these mechanisms will be pivotal to identify biomarkers that distinguish functional from NDDs in subjective cognitive decline (). Further studies may focus on the neurobiological mechanisms of the interaction between low education and cell senescence phenotypically presenting as cognitive impairment.

Medical diagnosis of major depressive disorder was significantly higher in individuals with FCD when compared with other groups. It is well known that mood disorders are often associated with subjective cognitive complaints or objective cognitive decline (). Besides, cognitive decline is described as a core symptom of depression, indicating that the impairment may also persist after the resolution of depressive symptoms and potentially worsen with repeated episodes (; ). Furthermore, individuals with major depression share a similar pattern of brain atrophy than MCI (), possibly indicating an irreversibility of cognitive manifestations of depression. Referral of individuals with FCD to tertiary memory clinics may have several negative consequences, such as delaying of proper medical care and potential for worsening of symptoms, especially with regard to the risk of suicide, both impacting the public health system.

In a public health context, uncovering the mist around individuals with FCD is beneficial for both patients and healthcare systems. The correct identification of individuals with FCD diminishes the delay between diagnosis and treatment, which improves their quality of life and the clinical management of untreated mental disorders (). This is especially important considering the referral process of public health systems, such as the Brazilian and the United Kingdom systems (), in which the primary care physician is in charge of appointments with specialists. Besides, adequate referral to neurological tertiary care should include patients with a high probability of a NDD, mitigating the financial burden of unnecessary imaging and laboratory exams (). Potential factors underlying the unnecessary referral of FCD to a tertiary memory service include the overidentification of age-related cognitive decline, a lack of training in recognizing functional complaints by primary care professionals, and the stigma present in the elderly with memory complaints. In our study, individuals with FCD were predominantly middle-aged and presented high MMSE scores, which is in agreement with previous studies (; ; ; ). In addition, we did not identify differences between the groups regarding cerebrovascular risk factors. In Brazil, the frequency of those risk factors is frequent in middle-aged individuals, which may explain the similarity between groups (). Additionally, a study found an association of poorer cardiovascular health and psychiatric disease ().

A few strategies may be implemented to optimize the identification and treatment of FCD in primary care and to decrease the number of referrals to a tertiary care level. Primarily, it is necessary to raise primary care physicians’ awareness that FCD is a common clinical entity with potential misdiagnosis with dementia (). Besides, efficient, continuous training for primary care physicians may improve the identification of FCD. In addition, brief screening scales for mood disorders are available in many languages, and it may be useful for general practitioners, such as 2-question screening scales for symptoms of depression () and anxiety (). Lastly, implementing and disclosing the usage of “dementia hotlines” may help identify FCD by general practitioners. Telehealth consultations have been described as critical in improving healthcare in small cities and avoiding unnecessary referrals (; ). Also, recent advances in the development of blood biomarkers promise to optimize referral processes in public health systems, owing mainly to their differential diagnosis capabilities (; ). Further studies may provide evidence in increasing the early identification of FCD in primary care settings and its impact in public health measures.

There are some limitations in this study. First, its retrospective design contributed to the missing data for many variables, such as education, MMSE and GDS, which may reduce the internal validity of the results. Second, as a tertiary service belonging to a public health system lacking specialists, patients with advanced stages of disease may have been referred preferentially, which may hamper the assessment of differences in cognitive tests between FCD and NDD groups. Missing values may also introduce bias, as they were not computed in the analysis. Lastly, it is important to mention that 2020 was atypical because of the COVID-19 pandemic and lockdown measures, which reduced the referral to all specialties, including neurology.

In conclusion, FCD is a common clinical entity among individuals with low educational setting, totaling around one-third of tertiary care referrals. Patients that presented with FCD were younger, showed higher MMSE and higher depressive scores than NDD individuals. Strategies to identify FCD in primary care settings may benefit both patients and healthcare systems, including long-term training for physicians and implementing dementia hotlines.

Publisher’s Note

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.

Statements

Data availability statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics statement

The studies involving human participants were reviewed and approved by the Comitê de Ética em Pesquisa do Hospital de Clinicas de Porto Alegre. Written informed consent for participation was not required for this study in accordance with the national legislation and the institutional requirements.

Author contributions

All authors listed have made a substantial, direct, and intellectual contribution to the work, and approved it for publication.

Funding

The publication of this study was funded by FIPE/HCPA. EZ receives funding from CNPq (435642/2018-9;312410/2018-2); Instituto Serrapilheira (Serra-1912 31365); Brazilian National Institute of Science and Technology in Excitotoxicity and Neuroprotection (465671/2014-4); FAPERGS/MS/CNPq/SESRS–PPSUS (30786.434.24734.23112017); ARD/FAPERGS (54392.632.30451.05032021) and Alzheimer’s Association (AAR GD-21-850670). RC receives funding from Alzheimer’s Association (AARGD-21-846545).

Conflict of interest

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.

Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fnagi.2022.789190/full#supplementary-material

References

Summary

Keywords

cognitive complaint, subjective cognitive decline, dementia, Alzheimer’s disease, public health, subjective memory impairment, major depression

Citation

Borelli WV, de Senna PN, Brum WS, Schumacher-Schuh AF, Zimmer ER, Fagundes Chaves ML and Castilhos RM (2022) Functional Cognitive Disorder Presents High Frequency and Distinct Clinical Profile in Patients With Low Education. Front. Aging Neurosci. 14:789190. doi: 10.3389/fnagi.2022.789190

Received

04 October 2021

Accepted

04 March 2022

Published

31 March 2022

Volume

14 - 2022

Edited by

Tania Araujo Viel, Universidade de São Paulo, Brazil

Reviewed by

Shuen Yee Lee, Singapore Institute of Technology, Singapore; Jeremy M. Silverman, Icahn School of Medicine at Mount Sinai, United States; Andrew Larner, The Walton Centre NHS Foundation Trust, United Kingdom

Updates

Copyright

*Correspondence: Wyllians Vendramini Borelli,

This article was submitted to Neurocognitive Aging and Behavior, a section of the journal Frontiers in Aging Neuroscience

Disclaimer

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.

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