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Genetic Association of Major Depression With Atypical Features and Obesity-Related Immunometabolic Dysregulations
Open accessAbstract
Importance: The association between major depressive disorder (MDD) and obesity may stem from shared immunometabolic mechanisms particularly evident in MDD with atypical features, characterized by increased appetite and/or weight (A/W) during an active episode. Objective: To determine whether subgroups of patients with MDD stratified according to the A/W criterion had a different degree of genetic overlap with obesity-related traits (body mass index [BMI] and levels of C-reactive protein [CRP] and leptin). Design, Setting, and Patients: This multicenter study assembled genome-wide genotypic and phenotypic measures from 14 data sets of the Psychiatric Genomics Consortium. Data sets were drawn from case-control, cohort, and population-based studies, including 26 628 participants with established psychiatric diagnoses and genome-wide genotype data. Data on BMI were available for 15 237 participants. Data were retrieved and analyzed from September 28, 2015, through May 20, 2017. Main Outcomes and Measures: Lifetime DSM-IV MDD was diagnosed using structured diagnostic instruments. Patients with MDD were stratified into subgroups according to change in the DSM-IV A/W symptoms as decreased or increased. Results: Data included 11 837 participants with MDD and 14 791 control individuals, for a total of 26 628 participants (59.1% female and 40.9% male). Among participants with MDD, 5347 (45.2%) were classified in the decreased A/W and 1871 (15.8%) in the increased A/W subgroups. Common genetic variants explained approximately 10% of the heritability in the 2 subgroups. The increased A/W subgroup showed a strong and positive genetic correlation (SE) with BMI (0.53 [0.15]; P = 6.3 × 10-4), whereas the decreased A/W subgroup showed an inverse correlation (-0.28 [0.14]; P = .06). Furthermore, the decreased A/W subgroup had a higher polygenic risk for increased BMI (odds ratio [OR], 1.18; 95% CI, 1.12-1.25; P = 1.6 × 10-10) and levels of CRP (OR, 1.08; 95% CI, 1.02-1.13; P = 7.3 × 10-3) and leptin (OR, 1.09; 95% CI, 1.06-1.12; P = 1.7 × 10-3). Conclusions and Relevance: The phenotypic associations between atypical depressive symptoms and obesity-related traits may arise from shared pathophysiologic mechanisms in patients with MDD. Development of treatments effectively targeting immunometabolic dysregulations may benefit patients with depression and obesity, both syndromes with important disability.
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“Obese individuals, particularly those presenting attributes of metabolic syndrome (abdominal obesity, hyperglycemia, hypertension, elevated triglycerides), tend to develop the atypical subtype [9] (Box 1).”
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Depression and obesity: evidence of shared biological mechanisms
Milaneschi, Y., Simmons, W. K., van Rossum, E. F. C., & Penninx, B. W. (2019) · Molecular Psychiatry · doi:10.1038/s41380-018-0017-5 · Cited by 1,073
“Recent large-scale analyses [31] involving >25,000 samples reported a strong genetic correlation (0.”
BackgroundInfluentialComorbid depression in medical diseases
Gold, S. M., Köhler‐Forsberg, O., Moss-Morris, R. E., Mehnert-Theuerkauf, A., Miranda, J. J., Bullinger, M., Steptoe, A., Whooley, M. A., & Otte, C. (2020) · Nature Reviews Disease Primers · doi:10.1038/s41572-020-0200-2 · Cited by 583
The menace of obesity to depression and anxiety prevalence
Fulton, S., Décarie-Spain, L., Fioramonti, X., Guiard, B., & Nakajima, S. (2022) · Trends in Endocrinology & Metabolism · doi:10.1016/j.tem.2021.10.005 · Cited by 441
“Obese individuals, particularly those presenting attributes of metabolic syndrome (abdominal obesity, hyperglycemia, hypertension, elevated triglycerides), tend to develop the atypical subtype [9] (Box 1).”
BackgroundDepression Heterogeneity and Its Biological Underpinnings: Toward Immunometabolic Depression
Milaneschi, Y., Lamers, F., Berk, M., & Penninx, B. W. J. H. (2020) · Biological Psychiatry · doi:10.1016/j.biopsych.2020.01.014 · Cited by 451
Machine learning in major depression: from classification to treatment outcome prediction
Gao, S., Calhoun, V. D., & Sui, J. (2018) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.13048 · Cited by 370
Metadata
- Authors
- Milaneschi, Y., Lamers, F., Peyrot, W. J., Baune, B. T., Breen, G., Dehghan, A., Forstner, A. J., Grabe, H. J., Homuth, G., Kan, C., Lewis, C., Mullins, N., Nauck, M., Pistis, G., Preisig, M., Rivera, M., Rietschel, M., Streit, F., Strohmaier, J., Teumer, A., Van der Auwera, S., Wray, N. R., Boomsma, D. I., Penninx, B. W. J. H., & for the CHARGE Inflammation Working Group and the Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
- Affiliations
- Amsterdam Neuroscience (NL)
- The University of Adelaide (AU)
- King's College London (GB)
- Imperial College London (GB)
- University of Bonn (DE)
- Universitätsmedizin Greifswald (DE)
- Centre Hospitalier Universitaire Vaudois (CH)
- Universidad de Granada (ES)
- Heidelberg University (DE)
- Department of Psychiatry and Psychotherapy, University Medicine Greifswald, Greifswald, Germany
- The University of Queensland (AU)
- Vrije Universiteit Amsterdam (NL)
- Corresponding author
- Milaneschi, Yuri
- ORCID
- Milaneschi, Yuri
- Lamers, Femke
- Peyrot, Wouter J.
- Baune, Bernhard T.
- Breen, Gerome
- Dehghan, Abbas
- Grabe, Hans J.
- Homuth, Georg
- Kan, Carol
- Lewis, Cathryn
- Mullins, Niamh
- Pistis, Giorgio
- Preisig, Martin
- Rivera, Margarita
- Rietschel, Marcella
- Streit, Fabian
- Strohmaier, Jana
- Teumer, Alexander
- Wray, Naomi R.
- Boomsma, Dorret I.
- Penninx, Brenda W. J. H.
- Venue
- JAMA Psychiatry
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- Published
- 2017-12-01
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- 74
- Issue
- 12
- Pages
- 1214
- ISSN
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- W2766503838
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- Universität Greifswald
- Ministry of Cultural Affairs
- National Institutes of Health (184.021.007, 389875, EU/QLRT-2001-01254, 1s10od018164-01, 1r01mh081802-01, MH66206, N01MH90003, AA13321, MH059542, AA13320, MH059541, DA12854)
- School of Medicine, Emory University
- University of North Carolina at Chapel Hill
- University of California, San Diego
- McDonnell Center for Systems Neuroscience
- Stanley Center for Psychiatric Research, Broad Institute
- Department of Psychiatry, University of Toronto
- Medical Research Council (G0701420, MR/K026992/1)
- Australian Research Council (FT0991360, FT0991022, 389875, QLG2-CT-2002-01254)
- Queensland Brain Institute
- Institute of Molecular and Cell Biology
- Statens Serum Institut
- Medizinische Fakultät der Albert-Ludwigs-Universität Freiburg
- National Institute on Alcohol Abuse and Alcoholism (R01AA014041, R01AA007535)
- National Institute of Mental Health (MH66206, MH068457, N01‐MH‐90003, U01MH109528, MH-081802, RC2MH089995, MH089951, MH109532, U24MH068457, MH085520, R01MH060912, U01MH109532, R01MH059552, RC2MH089951, R01MH061686, MH089995, R01MH080403)
- National Institute on Drug Abuse (K08DA019951)
- National Cancer Institute
- National Institute of Diabetes and Digestive and Kidney Diseases (U01DK066134)
- Janssen Research and Development
- Institute of Genetics
- Division of Cancer Epidemiology and Genetics, National Cancer Institute
- NHLBI Division of Intramural Research
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Life Sciences › Neuroscience › Biological Psychiatry › Tryptophan and brain disorders
- Health Sciences › Medicine › Pharmacology (medical) › Treatment of Major Depression
- Keywords
- major depressive disorder, atypical depression, obesity, genetic correlation, body mass index, C-reactive protein, leptin, polygenic risk, genetic overlap, Psychiatric Genomics Consortium, heritability
- MeSH terms
- Adult, C-Reactive Protein, Depressive Disorder, Major, Major Depressive Disorder, Female, Humans, International Cooperation, Male, Obesity, Psychiatric Status Rating Scales, Weight Gain, Body Mass Index, Genetic Predisposition to Disease, Diagnostic and Statistical Manual of Mental Disorders, Genome-Wide Association Study, Craving
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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