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Leptin and leptin receptor gene polymorphisms and depression treatment response
Department of Psychiatry, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Department of Psychiatry, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland; Department of Psychiatry, The Pirkanmaa Wellbeing Services County, Tampere, Finland.
Department of Clinical Chemistry, Tampere Univ. Hospital and Fimlab Laboratories and Finnish Cardiovascular Research Center-Tampere, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Department of Clinical Chemistry, Tampere Univ. Hospital and Fimlab Laboratories and Finnish Cardiovascular Research Center-Tampere, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
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2025 (Engelska)Ingår i: Acta Neuropsychiatrica, ISSN 0924-2708, E-ISSN 1601-5215, Vol. 37, artikel-id e38Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Objective: Associations between leptin (LEP) and leptin receptor (LEPR) gene polymorphisms and mood disorders have been found but not yet confirmed in multiple studies. The aim of our study was to study the associations between LEP and LEPR single nucleotide polymorphisms (SNPs) and treatment response of depression. Associations between leptin levels and depression severity were also investigated.

Methods: The data included 242 depressed patients in secondary psychiatric care. Symptoms of depression were assessed with the Montgomery-Asberg Depression Rating Scale (MADRS). Previously found LEP and LEPR SNPs associated with depression and other mood disorders were studied. Furthermore, all available LEP and LEPR SNPs were clumped using proxy SNPs to represent gene areas in r2 > 0.2 linkage disequilibrium and their association with treatment response was analysed with logistic regression.

Results: Two proxy SNPs of LEPR gene, rs12564738 and rs12029311, were associated with MADRS response at 6 weeks (p adjusted = 0.024, p adjusted = 0.024). SNPs from previous studies were not associated with MADRS response, but LEPR rs12145690 from a previous study was strongly associated with rs12564738 (r2 = 0.94). The positive association between leptin levels and MADRS score at baseline after adjusting with age, sex, body mass index (BMI), Alcohol Use Disorders Identification Test score, and smoking was found (p = 0.011).

Conclusion: Our findings suggest that LEPR polymorphisms are associated with depression treatment response. We also found associations between leptin levels and depression independently of BMI. Further studies and meta-Analyses are needed to confirm the significance of found SNPs and the role of leptin in depression.

Ort, förlag, år, upplaga, sidor
Cambridge University Press, 2025. Vol. 37, artikel-id e38
Nyckelord [en]
Depression, genetics, leptin, leptin receptor, treatment outcome
Nationell ämneskategori
Näringslära och dietkunskap
Identifikatorer
URN: urn:nbn:se:umu:diva-232286DOI: 10.1017/neu.2024.43ISI: 001353437400001PubMedID: 39529327Scopus ID: 2-s2.0-85209727418OAI: oai:DiVA.org:umu-232286DiVA, id: diva2:1916614
Forskningsfinansiär
Finlands Akademi, 356405EU, Horisont 2020, 848146Tillgänglig från: 2024-11-28 Skapad: 2024-11-28 Senast uppdaterad: 2025-05-28Bibliografiskt granskad

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Kampman, Olli

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