PMID- 35338947 OWN - NLM STAT- MEDLINE DCOM- 20220510 LR - 20220511 IS - 1873-3360 (Electronic) IS - 0306-4530 (Linking) VI - 140 DP - 2022 Jun TI - Diabetes, antidiabetic medications and risk of depression - A population-based cohort and nested case-control study. PG - 105715 LID - S0306-4530(22)00056-7 [pii] LID - 10.1016/j.psyneuen.2022.105715 [doi] AB - OBJECTIVE: Diabetes type 2 is associated with depression, but the impact of antidiabetic drugs is not clear. The objective was to analyze the association between diabetes type 2, antidiabetic drugs, and depression. METHODS: This register-based study included 116.699 patients with diabetes type 2 diagnosed from 2000 to 2012 and an age, gender, and municipality matched reference group of 116.008 individuals without diabetes. All participants were followed for a diagnosis of depression or prescription of antidepressant medication. Based on this, a case-control study was nested within the cohort, using risk set sampling. Antidiabetic medication was categorized into insulin, metformin, sulfonylureas and glinides combined, glitazones, dipeptidyl peptidase 4 (DPP4) inhibitors, glucagon-like peptide 1 (GLP1) analogs, sodium-glucose transport protein 2 (SGLT2) inhibitors and acarbose. The association between diabetes and depression was analyzed using Cox proportional hazards regression, whereas conditional logistic regression was used to analyze the association between use of antidiabetic drugs and depression. RESULTS: Patients with diabetes had higher risk of depression compared to individuals without diabetes (hazard ratio 1.14 (95% confidence interval 1.14-1.15)). Low doses of metformin, DPP4 inhibitors, GLP1 analogs, and SGLT2 inhibitors were associated with lower risk of depression in patients with diabetes compared to non-users, with the lowest risk for sodium-glucose transport protein 2 inhibitor users (odds ratio 0.55 (0.44-0.70)). Use of insulin, sulfonylurea and high doses of metformin were associated with higher risk of depression. CONCLUSION: Patients with diabetes had increased risk of depression. However, users of specific antidiabetic drugs had lower risk of depression compared to non-users. CI - Copyright (c) 2022 The Authors. Published by Elsevier Ltd.. All rights reserved. FAU - Wium-Andersen, Ida Kim AU - Wium-Andersen IK AD - Psychiatric Center Copenhagen, Region Hovedstadens Psykiatri, Edel Sauntes Alle 10, 2100 Copenhagen, Denmark. Electronic address: Ida.kim.wiumandersen@regionh.dk. FAU - Osler, Merete AU - Osler M AD - Center for Clinical Research and Prevention, Bispebjerg-Frederiksberg University Hospital, Nordre Fasanvej 57, 2000 Frederiksberg, Denmark; Section of Epidemiology, Department of Public Health, University of Copenhagen, Oster Farimagsgade 5, 1014 Copenhagen, Denmark. FAU - Jorgensen, Martin Balslev AU - Jorgensen MB AD - Psychiatric Center Copenhagen, Region Hovedstadens Psykiatri, Edel Sauntes Alle 10, 2100 Copenhagen, Denmark. FAU - Rungby, Jorgen AU - Rungby J AD - Department of Endocrinology, Bispebjerg-Frederiksberg University Hospital, Bispebjerg bakke 23, 2400 Copenhagen, Denmark; Copenhagen Center for Translational Research, Bispebjerg-Frederiksberg University hospital, Bispebjerg Bakke 23, 2400 Copenhagen, Denmark. FAU - Wium-Andersen, Marie Kim AU - Wium-Andersen MK AD - Center for Clinical Research and Prevention, Bispebjerg-Frederiksberg University Hospital, Nordre Fasanvej 57, 2000 Frederiksberg, Denmark. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20220315 PL - England TA - Psychoneuroendocrinology JT - Psychoneuroendocrinology JID - 7612148 RN - 0 (Dipeptidyl-Peptidase IV Inhibitors) RN - 0 (Hypoglycemic Agents) RN - 0 (Insulin) RN - 89750-14-1 (Glucagon-Like Peptide 1) RN - 9100L32L2N (Metformin) SB - IM MH - Case-Control Studies MH - Depression/drug therapy MH - *Diabetes Mellitus, Type 2/complications MH - *Dipeptidyl-Peptidase IV Inhibitors/adverse effects MH - Glucagon-Like Peptide 1 MH - Humans MH - Hypoglycemic Agents/adverse effects MH - Insulin/therapeutic use MH - *Metformin/adverse effects EDAT- 2022/03/27 06:00 MHDA- 2022/05/11 06:00 CRDT- 2022/03/26 20:08 PHST- 2021/08/20 00:00 [received] PHST- 2022/01/26 00:00 [revised] PHST- 2022/03/07 00:00 [accepted] PHST- 2022/03/27 06:00 [pubmed] PHST- 2022/05/11 06:00 [medline] PHST- 2022/03/26 20:08 [entrez] AID - S0306-4530(22)00056-7 [pii] AID - 10.1016/j.psyneuen.2022.105715 [doi] PST - ppublish SO - Psychoneuroendocrinology. 2022 Jun;140:105715. doi: 10.1016/j.psyneuen.2022.105715. Epub 2022 Mar 15.