Peripheral Biomarkers of Anorexia Nervosa: A Meta-Analysis

Author:

Wu Ya-Ke12ORCID,Watson Hunna J.234,Del Re Aaron C.56,Finch Jody E.7,Hardin Sabrina L.8,Dumain Alexis S.9ORCID,Brownley Kimberly A.2,Baker Jessica H.10

Affiliation:

1. School of Nursing, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA

2. Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA

3. School of Psychology, Curtin University, Bentley, WA 6102, Australia

4. School of Paediatrics, Division of Medicine, The University of Western Australia, Crawley, WA 6009, Australia

5. Del Re Data & Statistical Consulting, San Diego, CA 91910, USA

6. Department of Psychology, University of Kassel, 34127 Kassel, Germany

7. Department of Psychology, Georgia State University, Atlanta, GA 30302, USA

8. National Center for PTSD, VA Boston Healthcare System, Boston, MA 02130, USA

9. Department of Psychology and Neuroscience, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA

10. Equip Health, Inc., P.O. Box 131747, Carlsbad, CA 92013, USA

Abstract

The pathogenesis of anorexia nervosa (AN) has been hypothesized to involve several biological systems. However, reliable biomarkers for AN have yet to be established. This study was aimed to identify statistically significant and clinically meaningful peripheral biomarkers associated with AN. A systematic literature search was conducted to identify studies published in English from inception until 30 June 2022. We conducted two-level random-effects meta-analyses to examine the difference between AN and comparison groups across 52 distinct biomarkers and found that acylated ghrelin, adrenocorticotropic hormone (ACTH), carboxy-terminal collagen crosslinks (CTX), cholesterol, cortisol, des-acyl ghrelin, ghrelin, growth hormone (GH), obestatin, and soluble leptin receptor levels were significantly higher in cases of AN compared with those in non-AN controls. Conversely, C-reactive protein (CRP), CD3 positive, CD8, creatinine, estradiol, follicle-stimulating hormone (FSH), free thyroxine, free triiodothyronine, glucose, insulin, insulin-like growth factor 1 (IGF-1), leptin, luteinizing hormone, lymphocyte, and prolactin levels were significantly lower in AN compared with those in non-AN controls. Our findings indicate that peripheral biomarkers may be linked to the pathophysiology of AN, such as processes of adaptation to starvation. Scientific investigation into peripheral biomarkers may ultimately yield breakthroughs in personalized clinical care for AN.

Funder

National Institute of Nursing Research

National Institute of Mental Health

Publisher

MDPI AG

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