ORIGINAL RESEARCH article

Front. Immunol., 30 November 2022

Sec. Inflammation

Volume 13 - 2022 | https://doi.org/10.3389/fimmu.2022.949665

The top 100 most cited articles in the last two decades of atopic dermatitis: A bibliometric analysis

  • 1. Department of Allergy, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China

  • 2. Allergy Department, Beijing Key Laboratory of Precision Medicine for Diagnosis and Treatment of Allergic Diseases, National Clinical Research Center for Dermatologic and Immunologic Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China

  • 3. Department of Dermatology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, National Clinical Research Center for Dermatologic and Immunologic Diseases, Beijing, China

Article metrics

View details

10

Citations

4,5k

Views

2,3k

Downloads

Abstract

Background:

Atopic dermatitis (AD) is the leading cause of skin-related disease burden worldwide, affecting a large percentage of the population. Bibliometrics is the statistical analysis of academic literature in a certain field.

Objectives:

We aimed to perform the latest bibliometric analysis of atopic dermatitis literature.

Methods:

We searched the Web of Science database on 29th Nov 2021. We used the keywords “atopic dermatitis,” “atopic eczema,” and “eczema” for our search. All items published between 2001 and 2021 were included. The top 100 most cited articles were identified and analyzed.

Results:

Our study provided a detailed bibliometric analysis of the top 100 most cited articles on atopic dermatitis. These articles were published between 2002 and 2019 and were from 15 different countries, mostly in the USA and Germany. Most articles have focused on the pathogenesis and treatment of AD. The Journal of Allergy and Clinical Immunology made the greatest contribution to the top 100 list, with 28 articles. The most cited article originated from Lancet. The highest number of citations was seen in 2006, with 9220 citations, while the highest number of publications was seen in 2006 with 12 publications.

Conclusions:

Our study aims to provide physicians and researchers with a historical perspective for the scientific progress of atopic dermatitis, and help clinicians effectively obtain useful articles that have a significant impact on the field of atopic dermatitis.

Introduction

Atopic dermatitis (AD) is a chronic relapsing inflammatory skin disease, which is characterized by severe itching, dryness, and erythematous rashes (1). AD may seriously affect the quality of life of patients and their families due to intense pruritus, sleeping loss, psychosocial impact, and substantial economic burden caused by costs of medical treatment (2, 3). The prevalence of AD is approximately 20% among children and it ranges between 7% and 14% among adults (4).

The bibliometric study represents an important study type showing the main research focuses or hotspots and trend topics in a given field (5). It could provide a systematic description and visual representation of the structure of a particular field for physicians and researchers. So far, many dermatologists have published the most cited articles in the form of bibliometric analysis on topics such as hidradenitis suppurativa, rosacea, and psoriasis (68).

The purpose of our study was to analyze the top 100 most cited AD articles published in the biomedical literature during the last 20 years and pave the way for further investigations for AD.

Methods

Search strategy

We have compared the pros and cons for each of them based on AlRyalat et al’s study and we finally chose the Web of Science (WOS) core collection for our bibliometric analysis (9). An important reason for this choice is the availability of a precise and comprehensive description of highly cited papers and hot papers. This feature is not available in other databases. We searched the WOS core database (accessed: 2021-11-29) using the topic “eczema”, “atopic dermatitis”, and “atopic eczema” between 2002 and 2021. There were no limitations on document types or languages. The results were sorted in descending order according to the number of citations cited in the WOS. Two researchers (Lishan Zhang and Yibo Hou) independently screened the abstract to obtain qualified articles. Studies on AD or studies including AD as the main part were included in our analysis scope. Articles not relevant to AD were excluded from our analysis. Under the guidance of senior experts (Yueping Zeng and Jinlyu Sun), two researchers finally reached an agreement on the top 100 most cited articles (T100) list.

Data extraction and conversion

Data including titles, authors, countries, institutes, year of publication, journals of publication, article types, impact factors, and total citations were collected from the WOS core database to excel. The Countries and institutes were recorded based on the information of the first corresponding author. The types of articles were categorized by original research, review article, clinical trial, clinical study, and comment. Journal impact factors were derived from 2020 Journal Citation Reports. As we all know, a citation is an important metric that shows the quality and influence of an article. However, a certain amount of time should be allowed to pass after the publication of an article for it to reach a higher number of citations. In our study, the average citations per year (ACY) score was used to eliminate the time bias, which provides a fairer comparison for junior academics. ACY = citation times/(2021-publication year+1).

Bibliometric analysis

Bibliometrix R-package software, an open-source software, was used for conducting quantitative analysis in our study. R-package was developed by Aria and Cuccurullo and written in R language, which can help users without coding skills to perform bibliometric analysis (10). After installing R on our computer, data downloaded from WOS in Plain Text format was uploaded to the Biblioshiny app. The Biblioshiny interface provides us with a set of tools for conducting statistics. Besides, we classified the selected articles into four categories based on the research topic, including pathogenesis, prevention and treatment, epidemiology, and others. “Pathogenesis” includes studies on exploring the origination and development of AD; “prevention and treatment” includes studies on the prevention and treatment of AD; “epidemiology” is the study of diseases in populations, investigating how, when, and why they occur; “others” includes the studies that do not belong to the above categories.

Ethical statement

This research was designed as a bibliometric analysis of published studies and did not involve any animal experiments or unreported clinical trials of human beings. Thus, approval from an ethics committee was not required.

Results

A total of 37,937 documents were retrieved from the WOS Core Collection databases between 2002 and 2021. The top 100 most cited articles were listed in Table 1 and sorted in descending order according to the number of citations. For the study types of the T100 articles on AD, reviews accounted for 37%, followed by basic science researches 27%, clinical trials 21%, clinical studies 10%, comments 1%, and others 4%.

Table 1

RankArticleCitationsACY*Topic
1Asher M I, Montefort S, Bjorksten B, et al. Worldwide time trends in the prevalence of symptoms of asthma, allergic rhinoconjunctivitis, and eczema in childhood: ISAAC Phases One and Three repeat multicountry cross-sectional surveys. Lancet, 2006,368(9537):733-743.2814187.6Epidemiology
2Compton J G, Munro C S, Palmer C N A, et al. Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis. Nat Genet, 2006,38(4):441-446.1939129.27Pathogenesis
3Soumelis V, Reche P A, Kanzler H. Human epithelial cells trigger dendritic cell-mediated allergic inflammation by producing TSLP. Nat Immunol, 2002,3(7):673-80.150479.16Pathogenesis
4Ong P Y, Ohtake T, Brandt C, et al. Endogenous antimicrobial peptides and skin infections in atopic dermatitis. N Engl J Med, 2002,347(15):1151-1160.140373.84Pathogenesis
5Bieber T. Atopic dermatitis. N Engl J Med, 2008,358(14):1483-1494.1385106.54Pathogenesis
6Galli S J, Tsai M, Piliponsky A M. The development of allergic inflammation. Nature, 2008,454(7203):445-454.115989.15Pathogenesis
7Leung D Y, Boguniewicz M, Howell M D, et al. New insights into atopic dermatitis. J Clin Invest, 2004,113(5):651-657.107863.41Pathogenesis
8Leung D Y, Bieber T. Atopic dermatitis. Lancet, 2003,361(9352):151-160.104458Pathogenesis
9Weidinger S, Novak N. Atopic dermatitis. Lancet, 2016,387(10023):1109-1122.907181.4Pathogenesis
10Kong H, Oh J, Deming C. Temporal shifts in the skin microbiome associated with disease flares and treatment in children with atopic dermatitis. Genome Res, 2012,22(5):850-9.89999.89Pathogenesis
11Kalliomaki M, Salminen S, Poussa T, et al. Probiotics and prevention of atopic disease: 4-year follow-up of a randomised placebo-controlled trial. Lancet, 2003,361(9372):1869-1871.89649.78Prevention and treatment
12Simpson E L, Bieber T, Guttman-Yassky E, et al. Two Phase 3 Trials of Dupilumab versus Placebo in Atopic Dermatitis. N Engl J Med, 2016,375(24):2335-2348.818163.6Prevention and treatment
13Nestle F O, Di Meglio P, Qin J Z, et al. Skin immune sentinels in health and disease. Nat Rev Immunol, 2009,9(10):679-691.77964.92Pathogenesis
14Liew F Y, Pitman N I, McInnes I B. Disease-associated functions of IL-33: the new kid in the IL-1 family. Nat Rev Immunol, 2010,10(2):103-110.77170.09Pathogenesis
15Trifari S, Kaplan C D, Tran E H, et al. Identification of a human helper T cell population that has abundant production of interleukin 22 and is distinct from T(H)-17, T(H)1 and T(H)2 cells. Nat Immunol, 2009,10(8):864-871.76864Pathogenesis
16Beck L A, Thaci D, Hamilton J D. Dupilumab treatment in adults with moderate-to-severe atopic dermatitis. N Engl J Med, 2014,371(2):130-9.760108.57Prevention and treatment
17Greer F R, Sicherer S H, Burks A W. The Effects of Early Nutritional Interventions on the Development of Atopic Disease in Infants and Children: The Role of Maternal Dietary Restriction, Breastfeeding, Hydrolyzed Formulas, and Timing of Introduction of Allergenic Complementary Foods. Pediatrics, 2019,143(4): e20190281.741370.5Prevention and treatment
18Irvine A D, McLean W H, Leung D Y. Filaggrin mutations associated with skin and allergic diseases. N Engl J Med, 2011,365(14):1315-1327.70070Pathogenesis
19Madison K C. Barrier function of the skin: “la raison d’être” of the epidermis. J Invest Dermatol, 2003,121(2):231-41.68137.83Pathogenesis
20Boguniewicz M, Leung D Y. Atopic dermatitis: a disease of altered skin barrier and immune dysregulation. Immunol Rev, 2011,242(1):233-246.67667.6Pathogenesis
21Okada H, Kuhn C, Feillet H. The ‘hygiene hypothesis’ for autoimmune and allergic diseases: an update. Clin Exp Immunol, 2010,160(1):1-9.66360.27Pathogenesis
22Dillon S R, Sprecher C, Hammond A, et al. Interleukin 31, a cytokine produced by activated T cells, induces dermatitis in mice. Nat Immunol, 2004,5(7):752-760.65338.41Pathogenesis
23Ikoma A, Steinhoff M, Stander S, et al. The neurobiology of itch. Nat Rev Neurosci, 2006,7(7):535-547.63442.27Pathogenesis
24Eichenfield L F, Tom W L, Berger T G, et al. Guidelines of care for the management of atopic dermatitis: section 2. Management and treatment of atopic dermatitis with topical therapies. J Am Acad Dermatol, 2014,71(1):116-132.62989.86Prevention and treatment
25Sonkoly E, Muller A, Lauerma A I. IL-31: a new link between T cells and pruritus in atopic skin inflammation. J Allergy Clin Immunol, 2006,117(2):411-7.61040.67Pathogenesis
26Hay R J, Johns N E, Williams H C. The global burden of skin disease in 2010: an analysis of the prevalence and impact of skin conditions. J Invest Dermatol 2014,134(6):1527-1534.59785.29Epidemiology
27Penders J, Thijs C, van den Brandt P A, et al. Gut microbiota composition and development of atopic manifestations in infancy: the KOALA Birth Cohort Study. Gut, 2007,56(5):661-667.57040.71Epidemiology
28Nomura I, Goleva E, Howell M D, et al. Cytokine milieu of atopic dermatitis, as compared to psoriasis, skin prevents induction of innate immune response genes. J Immunol, 2003,171(6):3262-3269.56831.56Pathogenesis
29Salimi M, Barlow J L, Saunders S P. A role for IL-25 and IL-33-driven type-2 innate lymphoid cells in atopic dermatitis. J Exp Med, 2013,210(13):2939-50.56170.13Pathogenesis
30Smits H, Engering A, van der Kleij D, et al. Selective probiotic bacteria induce IL-10-producing regulatory T cells in vitro by modulating dendritic cell function through dendritic cell-specific intercellular adhesion molecule 3-grabbing nonintegrin. J Allergy Clin Immunol, 2005,115(6):1260-1267.54934.31Pathogenesis
31Allakhverdi Z, Comeau M R, Jessup H K, et al. Thymic stromal lymphopoietin is released by human epithelial cells in response to microbes, trauma, or inflammation and potently activates mast cells. J Exp Med, 2007,204(2):253-258.53938.5Pathogenesis
32Eichenfield L F, Tom W L, Chamlin S L, et al. Guidelines of care for the management of atopic dermatitis: section 1. Diagnosis and assessment of atopic dermatitis. J Am Acad Dermatol, 2014,70(2):338-351.53667Prevention and treatment
33Illi S, von Mutius E, Lau S, et al. The natural course of atopic dermatitis from birth to age 7 years and the association with asthma. J Allergy Clin Immunol, 2004,113(5):925-931.53531.47Epidemiology
34Kukkonen K, Savilahti E, Haahtela Tari. Probiotics and prebiotic galacto-oligosaccharides in the prevention of allergic diseases: a randomized, double-blind, placebo-controlled trial. J Allergy Clin Immunol, 2007,119(1):192-8.51234.13Prevention and treatment
35Sun Y G, Chen Z F.A gastrin-releasing peptide receptor mediates the itch sensation in the spinal cord. Nature, 2007,448(7154):700-3.50636.14Pathogenesis
36Wilson S R, The L, Batia L M, et al. The epithelial cell-derived atopic dermatitis cytokine TSLP activates neurons to induce itch. Cell, 2013,155(2):285-295.50262.75Pathogenesis
37Mendell M J, Mirer A G, Cheung K, et al. Respiratory and allergic health effects of dampness, mold, and dampness-related agents: a review of the epidemiologic evidence. Environ Health Perspect, 2011,119(6):748-756.50250.2Epidemiology
38Wang Y H, Angkasekwinai P, Lu N, et al. IL-25 augments type 2 immune responses by enhancing the expansion and functions of TSLP-DC-activated Th2 memory cells. J Exp Med, 2007,204(8):1837-1847.50135.79Pathogenesis
39Odhiambo J A, Williams H C, Clayton T O, et al.Global variations in prevalence of eczema symptoms in children from ISAAC Phase Three. J Allergy Clin Immunol, 2009,124(6):1251-8.e23.50041.67Epidemiology
40Howell M D, Kim B E, Gao P, et al. Cytokine modulation of atopic dermatitis filaggrin skin expression. J Allergy Clin Immunol, 2007,120(1):150-155.49935.64Pathogenesis
41Abrahamsson T R, Jakobsson H E, Andersson A F, et al. Low diversity of the gut microbiota in infants with atopic eczema. J Allergy Clin Immunol, 2012,129(2):434-440, 440-441.49555Pathogenesis
42Blauvelt A, de Bruin-Weller M, Gooderham M, et al. Long-term management of moderate-to-severe atopic dermatitis with dupilumab and concomitant topical corticosteroids (LIBERTY AD CHRONOS): a 1-year, randomised, double-blinded, placebo-controlled, phase 3 trial. Lancet, 2017,389(10086):2287-2303.494123.5Prevention and treatment
43Byrd A L, Belkaid Y, Segre J A. The human skin microbiome. Nat Rev Microbiol, 2018,16(3):143-155.491163.67Pathogenesis
44Gittler J K, Shemer A, Suarez-Farinas M, et al. Progressive activation of T(H)2/T(H)22 cytokines and selective epidermal proteins characterizes acute and chronic atopic dermatitis. J Allergy Clin Immunol, 2012,130(6):1344-1354.48253.56Pathogenesis
45Kim B S, Siracusa M C, Saenz S A, et al. TSLP elicits IL-33-independent innate lymphoid cell responses to promote skin inflammation. Sci Transl Med, 2013,5(170):170ra16.47659.5Pathogenesis
46Shaw T E, Currie G P, Koudelka C W, et al. Eczema prevalence in the United States: data from the 2003 National Survey of Children’s Health. J Invest Dermatol, 2011,131(1):67-73.47147.1Epidemiology
47Hongbo Y, Thomas C L, Harrison M A, et al. Translating the science of quality of life into practice: What do dermatology life quality index scores mean? J Invest Dermatol, 2005,125(4):659-664.46629.13Others
48Koga C, Kabashima K, Shiraishi N, et al. Possible pathogenic role of Th17 cells for atopic dermatitis. J Invest Dermatol, 2008,128(11):2625-2630.46435.69Pathogenesis
49Moro G, Arslanoglu S, Stahl B, et al. A mixture of prebiotic oligosaccharides reduces the incidence of atopic dermatitis during the first six months of age. Arch Dis Child, 2006,91(10):814-819.46330.87Prevention and treatment
50Sandilands A, Sutherland C, Irvine A D, et al. Filaggrin in the frontline: role in skin barrier function and disease. J Cell Sci, 2009,122(Pt 9):1285-1294.45638Pathogenesis
51Cork M J, Danby S G, Vasilopoulos Y, et al. Epidermal barrier dysfunction in atopic dermatitis. J Invest Dermatol, 2009,129(8):1892-1908.45537.92Pathogenesis
52Sidbury R, Davis DM, Cohen DE, et al. Guidelines of care for the management of atopic dermatitis. J Am Acad Dermatol, 2016,315(5):469-479.45464.86Prevention and treatment
53Nograles K E, Zaba L C, Shemer A, et al. IL-22-producing “T22” T cells account for upregulated IL-22 in atopic dermatitis despite reduced IL-17-producing TH17 T cells. J Allergy Clin Immunol, 2009,123(6):1244-1252.45437.83Pathogenesis
54Sandilands A, Terron-Kwiatkowski A, Hull P R, et al. Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema. Nat Genet, 2007,39(5):650-654.44631.86Pathogenesis
55Weidinger S, Illig T, Baurecht H, et al. Loss-of-function variations within the filaggrin gene predispose for atopic dermatitis with allergic sensitizations. J Allergy Clin Immunol, 2006,118(1):214-219.44629.73Pathogenesis
56Bisgaard H, Li N, Bonnelykke K, et al. Reduced diversity of the intestinal microbiota during infancy is associated with increased risk of allergic disease at school age. J Allergy Clin Immunol, 2011,128(3):646-52.e1-5.43643.6Epidemiology
57Steinhoff M, Neisius U, Ikoma A, et al. Proteinase-activated receptor-2 mediates itch: a novel pathway for pruritus in human skin. J Neurosci, 2003,23(15):6176-6180.43624.22Pathogenesis
58Basra M K, Fenech R, Gatt R M, et al. The Dermatology Life Quality Index 1994-2007: a comprehensive review of validation data and clinical results. Br J Dermatol, 2008,159(5):997-1035.43533.46Others
59Simpson E L, Chalmers J R, Hanifin J M, et al. Emollient enhancement of the skin barrier from birth offers effective atopic dermatitis prevention. J Allergy Clin Immunol, 2014,134(4):818-823.43261.71Prevention and treatment
60Yoo J, Omori M, Gyarmati D, et al. Spontaneous atopic dermatitis in mice expressing an inducible thymic stromal lymphopoietin transgene specifically in the skin. J Exp Med, 2005,202(4):541-549.43126.93Pathogenesis
61Bieber T. Atopic Dermatitis. Ann Dermatol, 2010,22(2):125-137.42738.82Pathogenesis
62Nakatsuji T, Chen T H, Narala S, et al. Antimicrobials from human skin commensal bacteria protect against Staphylococcus aureus and are deficient in atopic dermatitis. Sci Transl Med, 2017,9(378):eaah4680.424106Others
63Rosenfeldt V, Benfeldt E, Nielsen S D, et al. Effect of probiotic Lactobacillus strains in children with atopic dermatitis. J Allergy Clin Immunol, 2003,111(2):389-395.41523.06Prevention and treatment
64Nutten A. Atopic dermatitis: gobal epidemiology and risk factors. Ann Nutr Metab, 2015;66 (Suppl 1):8-16.40868Epidemiology
65Hammad H, Lambrecht B N. Barrier Epithelial Cells and the Control of Type 2 Immunity. Immunity, 2015,43(1):29-40.40868Pathogenesis
66Rautava S, Kalliomäki M, Isolauri E. Probiotics during pregnancy and breast-feeding might confer immunomodulatory protection against atopic disease in the infant. J Allergy Clin Immunol, 2002,109(1):119-21.40521.32Prevention and treatment
67Ziegler S F, Artis D. Sensing the outside world: TSLP regulates barrier immunity. Nat Immunol, 2010,11(4):289-293.38935.36Pathogenesis
68Homey B, Steinhoff M, Ruzicka T, et al. Cytokines and chemokines orchestrate atopic skin inflammation. J Allergy Clin Immunol, 2006,118(1):178-8938725.8Pathogenesis
69Taylor A L, Dunstan J A, prescott S L. Probiotic supplementation for the first 6 months of life fails to reduce the risk of atopic dermatitis and increases the risk of allergen sensitization in high-risk children: A randomized controlled trial. J Allergy Clin Immunol, 2007,119(1):184-91.38525.367Prevention and treatment
70Dunstan J A, Mori T A, Barden A, et al. Fish oil supplementation in pregnancy modifies neonatal allergen-specific immune responses and clinical outcomes in infants at high risk of atopy: a randomized, controlled trial. J Allergy Clin Immunol, 2003,112(6):1178-84.37720.94Prevention and treatment
71Weidinger S, Beck L A, Bieber T, et al. Atopic dermatitis. Nat Rev Dis Primers, 2018, 21;4(1):1.375125Pathogenesis
72Arslanoglu S, Moro G E, Schmitt J, et al. Early dietary intervention with a mixture of prebiotic oligosaccharides reduces the incidence of allergic manifestations and infections during the first two years of life. J Nutr, 2008,138(6):1091-5.37328.69Prevention and treatment
73Ring J, Alomar A, Bieber T, et al. Guidelines for treatment of atopic eczema (atopic dermatitis) part I. J Eur Acad Dermatol Venereol, 2012,26(8):1045-60.36740.78Prevention and treatment
74Morgenstern V, Zutavern A, Cyrys J, et al. Atopic diseases, allergic sensitization, and exposure to traffic-related air pollution in children. Am J Respir Crit Care Med, 2008,177(12):1331-7.36628.15Epidemiology
75Akids C A, Akdis M, Bieber T, et al. Diagnosis and treatment of atopic dermatitis in children and adults: European Academy of Allergology and Clinical Immunology/American Academy of Allergy, Asthma and Immunology/PRACTALL Consensus Report. Allergy, 2006,61(8):969-87.36124.07Prevention and treatment
76Williams H, Stewart A, von Mutius E, et al. Is eczema really on the increase worldwide? J Allergy Clin Immunol, 2008,121(4):947-54. e15.35927.62Epidemiology
77Cork M J, Robinson D A, Vasilopoulos, et al. New perspectives on epidermal barrier dysfunction in atopic dermatitis: gene-environment interactions. J Allergy Clin Immunol, 2006,118(1):3-21.35323.53Pathogenesis
78Horimukai K, Morita K, Narita M, et al. Application of moisturizer to neonates prevents development of atopic dermatitis. J Allergy Clin Immunol, 2014,134(4):824-830.e6.35150.14Prevention and treatment
79Williams H C. atopic dermatitis. N Engl J Med, 2005,352(22):2314-24.35021.88Prevention and treatment
80Viljanen M, Savilahti E, Haahtela T, et al. Probiotics in the treatment of atopic eczema/dermatitis syndrome in infants: a double-blind placebo-controlled trial. Allergy,2005,60(4):494-500.34921.81Prevention and treatment
81Gupta R, Sheikh A, Strachan D P, et al. Time trends in allergic disorders in the UK. Thorax, 2007,62(1):91-6.34724.79Epidemiology
82Cevikbas F, Wang X, Akiyama T, et al. sensory neuron-expressed IL-31 receptor mediates T helper cell-dependent itch: Involvement of TRPV1 and TRPA1. J Allergy Clin Immunol, 2014,133(2):448-60.34549.29Pathogenesis
83Wollenberg A, Wagner M, Günther S, et al. Plasmacytoid dendritic cells: a new cutaneous dendritic cell subset with distinct role in inflammatory skin diseases. J Invest Dermatol, 2002,119(5):1096-102.34418.11Pathogenesis
84Abrahamsson T R, Jakobsson T, Böttcher M F, et al. Probiotics in prevention of IgE-associated eczema: a double-blind, randomized, placebo-controlled trial. J Allergy Clin Immunol, 2007,119(5):1174-80.34324.5Prevention and treatment
85Benedetto A D, Rafaels N M, McGirt L Y, et al. Tight junction defects in patients with atopic dermatitis. J Allergy Clin Immunol, 2011,127(3):773-86.e1-7.33933.9Pathogenesis
86Thaci D, Simpson E L, Beck L A, et al. Efficacy and safety of dupilumab in adults with moderate-to-severe atopic dermatitis inadequately controlled by topical treatments: a randomised, placebo-controlled, dose-ranging phase 2b trial. Lancet, 2016,387(10013):40-52.33667.2Prevention and treatment
87Oetjen L K, Mack M R, Feng J, et al. Sensory Neurons Co-opt Classical Immune Signaling Pathways to Mediate Chronic Itch. Cell, 2017,171(1):217-228.e13.32882Pathogenesis
88Fallon P G, Sasaki T, Sandilands A, et al. A homozygous frameshift mutation in the mouse Flg gene facilitates enhanced percutaneous allergen priming. Nat Genet, 2009,41(5):602-8.32627.17Pathogenesis
89Jin H, He R, Oyoshi M, et al. Animal Models of Atopic Dermatitis. J Invest Dermatol, 2009,129(1):31-40.32527.08Others
90Kalliomäki M, Salminen S, Poussa T, et al. Probiotics during the first 7 years of life: a cumulative risk reduction of eczema in a randomized, placebo-controlled trial. J Allergy Clin Immunol, 2007,119(4):1019-21.32523.21Prevention and treatment
91Carroll C L, Balkrishnan R, Feldman S R, et al. The burden of atopic dermatitis: impact on the patient, family, and society. Pediatr Dermatol, 2005;22(3):192-9.32520.31Pathogenesis
92Elias P M, Hatano Y, Williams M L. Basis for the barrier abnormality in atopic dermatitis: Outside-inside-outside pathogenic mechanisms. J Allergy Clin Immunol, 2008,121(6):1337-43.32324.85Pathogenesis
93Devereux G, Seaton A. Diet as a risk factor for atopy and asthma. J Allergy Clin Immunol, 2005,115(6):1109-17.32220.13Epidemiology
94Silverberg J I, Hanifin J M. Adult eczema prevalence and associations with asthma and other health and demographic factors: a US population-based study. J Allergy Clin Immunol, 2013,132(5):1132-8.31839.75Epidemiology
95Brown S J, McLean W H I. One remarkable molecule: filaggrin. J Invest Dermatol, 2012,132(3 Pt 2):751-62.31735.22Pathogenesis
96Segre J A. Epidermal barrier formation and recovery in skin disorders. J Clin Invest, 2006,116(5):1150-8.31621.07Pathogenesis
97Ruzicka T, Mihara R. Anti-Interleukin-31 Receptor A Antibody for Atopic Dermatitis. N Engl J Med, 2017,376(21):2093.31578.75Prevention and treatment
98Huang J T, Abrams M, Tlougan B, et al. Treatment of Staphylococcus aureus colonization in atopic dermatitis decreases disease severity. Pediatrics, 2009,123(5):e808-14.31526.25Prevention and treatment
99Werfel T, Allam J P, Biedermann T, et al. Cellular and molecular immunologic mechanisms in patients with atopic dermatitis. J Allergy Clin Immunol, 2016,138(2):336-49.31262.4Pathogenesis
100Kim B E, Leung D Y M, Boguniewicz M, et al. Loricrin and involucrin expression is down-regulated by Th2 cytokines through STAT-6. Clin Immunol, 2008,126(3):332-7.31023.85Pathogenesis

The top 100 cited articles on atopic dermatitis.

ACY*- average citations per year.

Year of publication

The top 100 most cited articles were published between 2002 and 2019. Figure 1 showed the number of articles published during these 18 years. There was a peak in the region of 2006-2009. The largest number of articles published was 12, which occurred in 2006.

Figure 1

Figure 1

The number of articles published each year.

Citations

The number of citations ranged from 310 to 2814. We found that the most cited article on AD was a study conducted by Asher et al. with the following title, “Worldwide time trends in the prevalence of symptoms of asthma allergic rhinoconjunctivitis, and eczema in childhood: ISAAC Phases One and Three repeat multicountry cross-sectional surveys,” which was published in Lancet, and this article also had the second highest ACY score. The least cited article was “Loricrin and involucrin expression is down-regulated by Th2 cytokines through STAT-6”, which was published in Clinical Immunology. The annual total citations and average article citations per year are shown in Figure 2. The total number of citations was the highest in 2006, reaching 9220, and the most cited article also appeared in 2006. The average number of annual citations was constantly increasing. Additionally, we found that eight articles received more than 1000 citations, and half of them were published in Lancet and The New England Journal of Medicine.

Figure 2

Figure 2

The annual total citations and average annual citations. The orange line represents the average annual citations of the published articles in different year, and the blue line represent the average total citations.

Journal of publication

The 100 articles were published across 37 different journals. The Journal of Allergy and Clinical Immunology published the most (n=28), followed by The Journal of Investigative Dermatology (n=9), The New England Journal of Medicine (n=7), and Lancet (n=6). The top 10 journals were listed in Table 2 with their impact factors and quartile scores. There were 91 articles published in journals in which the “Quartile Score” category was Q1. Of the T100 articles, 74 were published in 24 journals that had an IF>10.

Table 2

JournalNumber of articlesImpact factorQuartile score
Journal of Allergy and Clinical Immunology2810.7931
Journal of Investigative Dermatology98.5511
New England Journal of Medicine791.2451
Lancet679.3211
Nature Immunology425.6061
Journal of Experimental Medicine414.3071
Nature Genetics338.332
Journal of the American Academy of Dermatology311.5271
Nature Reviews Immunology253.1061
Nature249.9621
Cell241.5821
Science Translational Medicine217.9561
Journal Clinical Investigation214.8081
Allergy213.1461
Pediatrics27.1251

Top 10 list of journals with published articles.

Countries and authors

The first corresponding authors of the 100 articles were from 15 different countries. According to the list, the USA (n=41) was the most contributing country, followed by Germany (n=18) and the United Kingdom (n=17) (Table 3). The highest-ranking 10 authors in the T100 cited articles were listed in Table 4. We found that Prof. Donald Leung, from the University of Colorado, produced the most top-cited articles on AD (n=12), followed by Prof. Thomas Bieber (n=10).

Table 3

CountryNumber of articles
USA41
Germany18
United Kingdom17
Finland5
Netherlands3
Australia2
Denmark2
Japan2
New Zealand2
Sweden2

Top 10 list of geographic origin.

Table 4

Corresponding authorNumber of articles
Donald Y.M. Leung12
Thomas Bieber10
Mark Boguniewicz8
W.H. Irwin Mclean8
Eric L. Simpson8
Jon M. Hanifin7
Alan D. Irvine7
Hywel C. Williams7
Lisa A. Beck6
Emma Guttman-Yassky5
Bernhard Homey5
Martin Steinhoff5
Stephan Weidinger5
Andreas Wollenberg5

Top 10 authors with the most published articles.

Keywords analysis, co-occurrence network, and trend topics

Analysis of authors’ most used keywords is an important tool for exploring hot topics in this field and scholars’ focus. The word cloud in Figure 3 showed the frequently used keywords were asthma, filaggrin, and skin barrier besides eczema. In addition, we investigated the keywords’ co-occurrence network to reveal the connections between keywords in works of literature (Figure 4). Notably, filaggrin played an important role in the co-occurrence network. Trend topics analysis gave further insight into the trending topics in terms of keyword occurrences in AD literature over the years (Figure 5). While conducting the analysis, the following parameters were configured. The search field was set to abstract. Word minimum frequency was set to 40 and the number of words per year was set to 2. Cytokines and skin barriers were the most discussed topic between 2006 and 2013. The result also showed that dupilumab (the first biologic agent approved for patients with moderate to severe AD) became a trending topic since 2015.

Figure 3

Figure 3

A visualized word cloud of frequently used keywords in the T100 list. The font size represents the number of repetitive keywords.

Figure 4

Figure 4

A co-occurrence networks. Thick lines indicate a strong relationship between those keywords. Thin lines represent weak association. Keywords without connecting lines indicate that no relationship has been established.

Figure 5

Figure 5

The trend topics analysis presents the hierarchical arrangement of topics in atopic dermatitis (AD) discussed by scholars per year. il, interleukin.

Discussion

AD is the most common chronic inflammatory skin disease in many developed countries (11). Recent trends have indicated that the prevalence of AD has increased in industrialized countries in recent decades and poses a significant burden on population health and healthcare settings (12). As we all know, citation analysis can provide comprehensive information about journals, institutions, and authors, which is available for identifying landmark papers and high-impact journals. Although it may not be possible to present a detailed analysis of all 100 top-cited articles, some features could be found. The bibliometric analysis can not only provide a deep insight into the most popular topics of AD in the past but also reveal the trend of AD research (13).

We found that in our T100, 36% of the articles were published less than 10 years prior, while 64% of them were more than 10 years before. However, the total ACY from 2002 to 2010 (ACY=2618) was lower than those from 2011 to 2019 (ACY=3065). It demonstrated that researchers paid more attention to AD in recent years. Although the 100 top-cited articles appeared in a total of 37 different journals, The Journal of Allergy and Clinical Immunology, Lancet, Cell, Nature, and The New England Journal of Medicine, were the main sources for nearly half of the articles (n=45). We found that core papers related to AD were published in a few top journals and these papers basically covered the overall situations of this field. This finding is consistent with Bradford’s law (14), which estimates the exponentially diminishing returns of extending a search for references in science journals and is commonly applied to determine the core journals in a specific field. Therefore, reading a few top journals could help busy dermatologists to keep updated in this field.

In addition, we noticed that all the articles with a marked influence came from developed countries. However, the latest available data from ISAAC (The International Study of Asthma and Allergies in Childhood), the largest worldwide collaborative research project, showed that AD continued to increase in prevalence specifically in developing countries, such as Latin America or South East Asia (15). Developing countries’ authors have limited involvement mainly due to the imbalance of global health resources between developed countries and developing countries (16).

The Biblioshiny app screens the themes of the literature according to the frequency of keywords in the selected literature. Sometimes it may not be able to reflect the main content of the article well. Therefore, we summarized the topic of the article manually. Articles were classified into one of the following four domains: pathogenesis, prevention and treatment, epidemiology, and others (Figure 6 and Table 1). Studies related to pathogenesis occupied the most articles (n=56). Extensive research has shed light on the multifaceted pathogenesis of the disease. Although an increasing number of studies have focused on AD, the etiology and pathogenesis of AD remain unclear. The bibliometric analysis shows that AD results from interactions among susceptibility, the environment, food allergy, skin barrier defects, gut microbial alterations, and immune disorders. Of these pathogenesis factors, the most critical one is skin barrier function. The most cited pathogenesis-related article was published in 2006, titled “Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis”. This work demonstrated that impaired skin barrier function played a key role in the development of atopic disease. In addition, 15 articles proved that immune cells (Th2 and Th17 cells) and related cytokines (IL-31, IL-25, IL-33, and TSLP) involved in the inflammatory response played an indispensable role in AD. These findings have reflected the direction of research in the last 20 years, and will form an important basis for future research for developing new therapeutic modalities.

Figure 6

Figure 6

Research topic of published research articles.

Recent developments in the understanding of AD pathogenesis have provided multiple options for treatments. In addition to the conventional therapies (application of moisturizers, topic corticosteroids, and immunosuppressants), targeted drugs including biologics and Janus kinase (JAK) inhibitors have been introduced as new options for AD. Of the T100 list, 26% were related to AD therapy. Sorting the literature in descending order of publication year, we observed that clinical trials on the safety and effectiveness of dupilumab were at the top ten list. The most cited article about dupilumab was a clinical trial published in the New England Journal of Medicine, titled “Two Phase 3 Trials of Dupilumab versus Placebo in Atopic Dermatitis”. It is only a 5-year-old article; however, it has 818 citations with an ACY score of 163.6 (rank: fifth). Dupilumab was the first biologic approved for moderate-to-severe AD and has become one of the most promising treatments for AD. Until the emergence of dupilumab, corticosteroids and immunosuppressant agents were the first-line therapies for rapid control of moderate-to-severe AD. Compared with conventional immunosuppressive therapy, dupilumab has good safety and can be used for the long-term treatment of AD (17). However, high cost may be a major consideration for dupilumab. To date, dupilumab has been approved for the remedy of type 2 immune diseases, such as asthma, and chronic rhinosinusitis with nasal polyps. Dupilumab will be used to relieve unmet clinical needs in other type 2 inflammation-related diseases (18). Furthermore, numerous biologics are now under investigation, including anti-IL-31RA monoclonal antibodies (nemolizumab) and anti-IL-13 monoclonal antibodies (tralokinumab and lebrikizumab). Besides, JAK inhibitors represent an emerging treatment option for AD. Abrocitinib, upadacitinib, and baricitinib are three oral JAK inhibitors approved for treating patients with AD, along with topical drugs ruxolitinib and delgocitinib. However, additional real-world studies are necessary to provide valuable data on the response and tolerability of these JAK inhibitors. The Global Burden of Disease has reported that skin diseases continue to be the fourth largest cause of nonfatal disease burden and AD accounts for the highest disease burden among skin diseases (19). Among the T100 list, there were fourteen articles related to the epidemiology of AD. One was a large multicenter cross-sectional survey conducted by Asher et al. and published in the Lancet, which has the highest citation number in the T100 list. Measuring the frequency of AD in a population and identifying how the disease frequency may differ over time or among subgroups are important steps in discovering potential causes and determining effective methods for prevention and care.

When we looked at the T100 list, another point of interest also caught our attention: the relationship between AD and intestinal microflora or skin microflora. Evidence suggested that skin and gut microbes might affect the course of AD. Six articles introduced research in this area. The most cited one was published in Genome Research, titled “Temporal shifts in the skin microbiome associated with disease flares and treatment in children with atopic dermatitis”. Studies indicated that an imbalance of the intestinal flora might be a factor leading to the deterioration of AD. Scientists have also proposed that the application of probiotics can regulate intestinal health by affecting the quantity and abundance of the intestinal microflora and modulating AD progression. Although several articles have described the efficacy of probiotics in AD, the exact curative effect remains uncertain.

In conclusion, this study identified the top 100 most cited articles on AD and analyzed their bibliometric characteristics, which may facilitate further research. However, there are still some shortcomings and limitations in our study. Firstly, the number of citations used did not exclude self-citations. Secondly, we only used the WOS database to conduct our research. Therefore, the list would be different if other databases were used.

Funding

This study was supported by the National High Level Hospital Clinical Research Funding (2022-PUMCH-B-092; Dr. YZ); the National Natural Science Foundation of China (81602765; Dr. YZ), (81971515; Dr. JS).

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.

Author contributions

YZ, JS contributed to conception and design of the study. LZ, YH performed the statistical analysis and wrote the first draft of the manuscript. All authors contributed to manuscript revision, read, and approved the submitted version.

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.

References

  • 1

    BantzSKZhuZZhengT. The atopic march: Progression from atopic dermatitis to allergic rhinitis and asthma. J Clin Cell Immunol (2014) 5(2):202. doi: 10.4172/2155-9899.1000202

  • 2

    AriënsLFMvan NimwegenKJMShamsMde BruinDTvan der SchaftJvan Os-MedendorpHet al. Economic burden of adult patients with moderate to severe atopic dermatitis indicated for systemic treatment. Acta Derm Venereol. (2019) 99(9):762–8. doi: 10.2340/00015555-3212

  • 3

    NaCHChungJSimpsonEL. Quality of life and disease impact of atopic dermatitis and psoriasis on children and their families. Children (Basel) (2019) 6(12):133. doi: 10.3390/children6120133

  • 4

    BylundSKobyletzkiLBSvalstedtMSvenssonA. Prevalence and incidence of atopic dermatitis: A systematic review. Acta Derm Venereol (2020) 100(12):adv00160. doi: 10.2340/00015555-3510

  • 5

    EllegaardOWallinJA. The bibliometric analysis of scholarly production: How great is the impact? Scientometrics (2015) 105(3):1809–31. doi: 10.1007/s11192-015-1645-z

  • 6

    SeivrightJThompsonAVillaNShiVHsiaoJ. Bibliometric analysis of the 50 most cited publications in hidradenitis suppurativa. Skin Appendage Disord (2021) 85(3):B182. doi: 10.1159/000513771

  • 7

    DaouLHageSEWakimESafiSSalamehP. Psoriasis: A bibliometric analysis in the Arab world (2004-2019). Australas J Dermatol (2021) 62(1):e19–23. doi: 10.1111/ajd.13407

  • 8

    WangYZhangHFangRTangKSunQ. The top 100 most cited articles in rosacea: a bibliometric analysis. J Eur Acad Dermatol Venereol (2020) 34(10):2177–82. doi: 10.1111/jdv.16305

  • 9

    AlRyalatSASMalkawiLWMomaniSM. Comparing bibliometric analysis using PubMed, scopus, and web of science databases. J Vis Exp (2019) 24(152):e58494. doi: 10.3791/58494

  • 10

    AriaMCuccurulloC. Bibliometrix: An r-tool for comprehensive science mapping analysis. J Informetrics (2017) 11(4):959–75. doi: 10.1016/j.joi.2017.08.007

  • 11

    BarbarotSAuziereSGadkariAGirolomoniGPuigLSimpsonELet al. Epidemiology of atopic dermatitis in adults: Results from an international survey. Allergy (2018) 73(6):1284–93. doi: 10.1111/all.13401

  • 12

    SweeneyASampathVNadeauKC. Early intervention of atopic dermatitis as a preventive strategy for progression of food allergy. Allergy Asthma Clin Immunol (2021) 17(1):30. doi: 10.1186/s13223-021-00531-8

  • 13

    TiernoaNRGonzalez-CruzTFMartinezJL. An overview of qualitative comparative analysis: a bibliometric analysis. J Innov Knowl (2017) 2(1):1523. doi: 10.1016/j.jik.2016.12.002

  • 14

    BroolesBC. Bradford’s law and the bibliography of science. Nature (1969) 224(5223):953–6. doi: 10.1038/224953a0

  • 15

    MallolJCraneJvon MutiusEOdhiamboJKeilUStewartAet al. ISAAC phase three study group: The international study of asthma and allergies in childhood (ISAAC) phase three: a global synthesis. Allergol Immunopathol (Madr) (2013) 41:7385. doi: 10.1016/j.aller.2012.03.001

  • 16

    GautierLSieleunouIKaloloA. Deconstructing the notion of “global health research partnerships” across northern and African contexts. BMC Med Ethics. (2018) 19(Suppl 1):49. doi: 10.1186/s12910-018-0280-7

  • 17

    DeleuranMThaçiDBeckLAde Bruin-WellerMBlauveltAFormanSet al. Dupilumab shows long-term safety and efficacy in patients with moderate to severe atopic dermatitis enrolled in a phase 3 open-label extension study. J Am Acad Dermatol (2020) 82(2):377–88. doi: 10.1016/j.jaad.2019.07.074

  • 18

    MatsunagaKKatohNFujiedaSIzuharaKOishiK. Dupilumab: Basic aspects and applications to allergic diseases. Allergology Int (2020) 69(2):187–96. doi: 10.1016/j.alit.2020.01.002

  • 19

    LaughterMRMaymoneMBCMashayekhiSArentsBWMKarimkhaniCLanganSMet al. The global burden of atopic dermatitis: lessons from the global burden of disease study 1990-2017. Br J Dermatol (2021) 184(2):304–9. doi: 10.1111/bjd.19580

Summary

Keywords

atopic dermatitis, bibliometric analysis, pathogenesis, treatment, eczema

Citation

Zhang L, Hou Y, Sun J and Zeng Y (2022) The top 100 most cited articles in the last two decades of atopic dermatitis: A bibliometric analysis. Front. Immunol. 13:949665. doi: 10.3389/fimmu.2022.949665

Received

21 May 2022

Accepted

09 November 2022

Published

30 November 2022

Volume

13 - 2022

Edited by

Nanette Silverberg, Icahn School of Medicine at Mount Sinai, United States

Reviewed by

Jarmila Celakovska, Charles University, Czechia; Alvise Sernicola, University of Padua, Italy

Updates

Copyright

*Correspondence: Yueping Zeng, ; Jinlyu Sun,

This article was submitted to Inflammation, a section of the journal Frontiers in Immunology

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.

Outline

Figures

Cite article

Copy to clipboard


Export citation file


Share article

Article metrics