PMID- 37087083 OWN - NLM STAT- MEDLINE DCOM- 20230612 LR - 20230612 IS - 1873-0183 (Electronic) IS - 1568-9972 (Linking) VI - 22 IP - 7 DP - 2023 Jul TI - Biomarkers in alopecia Areata: A systematic review and meta-analysis. PG - 103339 LID - S1568-9972(23)00073-3 [pii] LID - 10.1016/j.autrev.2023.103339 [doi] AB - BACKGROUND: Alopecia areata (AA) is an autoimmune non-scarring alopecia that affects the scalp or any hair-bearing areas in the body. The pathophysiology of AA is complex, but Th1, Th2, and Th17 cytokines dysregulation, as well as chemokines, immunoglobulins and other biomarkers have been shown to play a role in the pathogenesis of the disease. OBJECTIVE: To conduct a systematic review and Meta-analysis to identify biomarkers that reflect AA activity and severity that could be used to better assess disease activity and response in both trials and clinical practice. METHODS: A literature search was conducted using the PUBMED, EMBASE and the Cumulative Index to Nursing and Allied Health Literature (CINAHL) from inception to December 2021. Articles reporting on associations between AA and serum clinical biomarkers (cytokines, chemokines, antibodies, immunoglobulins, and others) were included. Serum biomarkers were identified in patients with AA and were correlated with disease severity and patient characteristics (ex. age, sex, comorbidities). The quality of the studies was assessed using the National Heart, Lung, and Blood Institute's Quality Assessment Tool for Case-Control Studies. Meta-analysis pooling of the standardized mean differences (SMD) by the method of Cohen using the common-effect inverse-variance model was performed. For the Meta-analysis, data was pulled for all the markers with a minimum of 4 studies with means and standard deviations. Analysis of data reported as Median with range or inter-quartile range (IQR) revealed that the data was too skewed to recommend calculation and use of mean with standard deviation (SD). If the data were not skewed, mean and SD were calculated. RESULTS: One thousand seven hundred fourteen studies were screened, with 91 included, reporting on a total of 52 biomarkers. Meta-analyses revealed pooled SMD that were significant for interleukin 6 (IL6), C-reactive protein (CRP) and vitamin D. CONCLUSIONS: Serum IL6 and CRP levels are significantly increased in patients with AA compared to healthy age and sex matched controls. Conversely, serum vitamn D levels are significantly decreased in patients with AA compared to healthy age and sex matched controls. This data has the potential to influence the clinical guidelines for the diagnostic workup of AA to include testing the serum levels of CRP and vitamin D. CI - Copyright (c) 2023 Elsevier B.V. All rights reserved. FAU - Zaaroura, Hiba AU - Zaaroura H AD - Division of Dermatology, Department of Paediatric Medicine, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada. FAU - Gilding, Anthony J AU - Gilding AJ AD - Canadian Alopecia Areata Foundation, Toronto, ON, Canada.; Department of Chemistry & Biology, Faculty of Science, Toronto Metropolitan University, Toronto, ON, Canada. FAU - Sibbald, Cathryn AU - Sibbald C AD - Division of Dermatology, Department of Paediatric Medicine, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada. Electronic address: cathryn.sibbald@mail.utoronto.ca. LA - eng PT - Journal Article PT - Meta-Analysis PT - Review PT - Systematic Review DEP - 20230420 PL - Netherlands TA - Autoimmun Rev JT - Autoimmunity reviews JID - 101128967 RN - 0 (Interleukin-6) RN - 0 (Biomarkers) RN - 0 (Cytokines) RN - 1406-16-2 (Vitamin D) RN - 0 (Chemokines) RN - 9007-41-4 (C-Reactive Protein) RN - 0 (Vitamins) RN - Diffuse alopecia SB - IM MH - Humans MH - *Alopecia Areata/diagnosis/pathology MH - Interleukin-6 MH - Biomarkers MH - Cytokines/metabolism MH - Vitamin D MH - Chemokines MH - C-Reactive Protein MH - Vitamins OTO - NOTNLM OT - Alopecia areata OT - Biomarker OT - Chemokine OT - Cytokine OT - Immunoglobulin COIS- Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Cathryn SIbbald reports a relationship with Pfizer that includes: consulting or advisory, funding grants, and speaking and lecture fees. Cathryn SIbbald reports a relationship with AbbVie Inc. that includes: consulting or advisory. Cathryn SIbbald reports a relationship with LEO Pharma Inc. that includes: consulting or advisory. Cathryn SIbbald reports a relationship with Novartis that includes: speaking and lecture fees. Cathryn SIbbald reports a relationship with Arcutis Biotherapeutics, Inc. that includes: speaking and lecture fees. EDAT- 2023/04/23 00:41 MHDA- 2023/06/12 06:42 CRDT- 2023/04/22 19:29 PHST- 2023/03/22 00:00 [received] PHST- 2023/04/13 00:00 [accepted] PHST- 2023/06/12 06:42 [medline] PHST- 2023/04/23 00:41 [pubmed] PHST- 2023/04/22 19:29 [entrez] AID - S1568-9972(23)00073-3 [pii] AID - 10.1016/j.autrev.2023.103339 [doi] PST - ppublish SO - Autoimmun Rev. 2023 Jul;22(7):103339. doi: 10.1016/j.autrev.2023.103339. Epub 2023 Apr 20.