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The bidirectional longitudinal association between depressive symptoms and HbA(1c): A systematic review and meta‐analysis

AIM: To investigate whether there is a bidirectional longitudinal association of depression with HbA(1c). METHODS: We conducted a systematic literature search in PubMed, PsycINFO, CINAHL and EMBASE for observational, longitudinal studies published from January 2000 to September 2020, assessing the a...

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Detalles Bibliográficos
Autores principales: Beran, Magdalena, Muzambi, Rutendo, Geraets, Anouk, Albertorio‐Diaz, Juan Rafael, Adriaanse, Marcel C., Iversen, Marjolein M., Kokoszka, Andrzej, Nefs, Giesje, Nouwen, Arie, Pouwer, Frans, Huber, Jörg W., Schmitt, Andreas, Schram, Miranda T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9292323/
https://www.ncbi.nlm.nih.gov/pubmed/34407250
http://dx.doi.org/10.1111/dme.14671
Descripción
Sumario:AIM: To investigate whether there is a bidirectional longitudinal association of depression with HbA(1c). METHODS: We conducted a systematic literature search in PubMed, PsycINFO, CINAHL and EMBASE for observational, longitudinal studies published from January 2000 to September 2020, assessing the association between depression and HbA(1c) in adults. We assessed study quality with the Newcastle‐Ottawa‐Scale. Pooled effect estimates were reported as partial correlation coefficients (r(p)) or odds ratios (OR). RESULTS: We retrieved 1642 studies; 26 studies were included in the systematic review and eleven in the meta‐analysis. Most studies (16/26) focused on type 2 diabetes. Study quality was rated as good (n = 19), fair (n = 2) and poor (n = 5). Of the meta‐analysed studies, six investigated the longitudinal association between self‐reported depressive symptoms and HbA(1c) and five the reverse longitudinal association, with a combined sample size of n = 48,793 and a mean follow‐up of 2 years. Higher levels of baseline depressive symptoms were associated with subsequent higher levels of HbA(1c) (partial r = 0.07; [95% CI 0.03, 0.12]; I(2)38%). Higher baseline HbA(1c) values were also associated with 18% increased risk of (probable) depression (OR = 1.18; [95% CI 1.12,1.25]; I(2)0.0%). CONCLUSIONS: Our findings support a bidirectional longitudinal association between depressive symptoms and HbA(1c). However, the observed effect sizes were small and future research in large‐scale longitudinal studies is needed to confirm this association. Future studies should investigate the role of type of diabetes and depression, diabetes distress and diabetes self‐management behaviours. Our results may have clinical implications, as depressive symptoms and HbA(1c) levels could be targeted concurrently in the prevention and treatment of diabetes and depression. REGISTRATION: PROSPERO ID CRD42019147551.