Somatic and sociodemographic predictors of depression outcome among depressed patients with coronary artery disease - a secondary analysis of the SPIRR-CAD study
Autor: | Martina de Zwaan, Jana Jünger, Martin Hellmich, Karl-Heinz Ladwig, Hans-Christian Deter, Frank Vitinius, Matthias Michal, Katja Petrowski, Cora Weber, Steffen Escherich, Christoph Herrmann-Lingen, Frank Lambertus, Christian Albus, Joram Ronel |
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Jazyk: | angličtina |
Rok vydání: | 2019 |
Předmět: |
Male
medicine.medical_specialty lcsh:RC435-571 Comorbidity Coronary Artery Disease Logistic regression Hospital Anxiety and Depression Scale law.invention Coronary artery disease 03 medical and health sciences 0302 clinical medicine Percutaneous Coronary Intervention Randomized controlled trial law Internal medicine lcsh:Psychiatry Outcome Assessment Health Care Medicine Heart rate variability Humans 030212 general & internal medicine Myocardial infarction Adverse effect Depression (differential diagnoses) Aged business.industry Depression Social Support Middle Aged medicine.disease 3. Good health 030227 psychiatry ddc Psychiatry and Mental health Medically Unexplained Symptoms Treatment Outcome Socioeconomic Factors Mental Disorders Coronary Heart Disease Psychotherapy Type D Personality Female business Depression - mental disorders - coronary heart disease - psychotherapy - type D personality Research Article |
Zdroj: | BMC Psychiatry, Vol 19, Iss 1, Pp 1-9 (2019) BMC Psychiatry 19:57 (2019) BMC Psychiatry |
DOI: | 10.1186/s12888-019-2026-6 |
Popis: | Background Depressive symptoms are common in patients with coronary artery disease (CAD) and are associated with an unfavourable outcome. Establishing prognostic patient profiles prior to the beginning of mental health care may facilitate higher efficacy of targeted interventions. The aim of the current study was to identify sociodemographic and somatic predictors of depression outcome among depressed patients with CAD. Methods Based on the dataset of the multicentre SPIRR-CAD randomised controlled trial (n = 570 patients with CAD and ≥ 8 points on the Hospital Anxiety and Depression Scale (HADS)), 141 potential sociodemographic and somatic predictors of the change in the HADS-D depression score from baseline to 18-month-follow-up were derived in two different ways. We screened for univariable association with response, using either analysis of (co)variance or logistic regression, respectively, both adjusted for baseline HADS-D value and treatment group. To guard against overfitting, multivariable association was evaluated by a linear or binomial (generalised) linear model with lasso regularisation, a machine learning approach. Outcome measures were the change in continuous HADS-D depression scores, as well as three established binary criteria. The Charlson Comorbidity Index (CCI) was calculated to assess possible influences of comorbidities on our results and was also entered in our machine learning approach. Results Higher age (p = 0.002), unknown previous myocardial infarction (p = 0.013), and a higher heart rate variability during numeracy tests (p = .020) were univariably associated with a favourable depression outcome, whereas hyperuricemia (p ≤ 0.003), higher triglycerides (p = 0.014), NYHA class III (p ≤ 0.028), state after resuscitation (p ≤ 0.042), intake of thyroid hormones (p = 0.007), antidiabetic drugs (p = 0.015), analgesic drugs (p = 0.027), beta blockers (p = 0.035), uric acid drugs (p ≤ 0.039), and anticholinergic drugs (p = 0.045) were associated with an adverse effect on the HADS-D depression score. In all analyses, no significant differences between study arms could be found and physical comorbidities also had no significant influence on our results. Conclusion Our findings may contribute to identification of somatic and sociodemographic predictors of depression outcome in patients with CAD. The unexpected effects of specific medication require further clarification and further research is needed to establish a causal association between depression outcome and our predictors. Trial registration www.clinicaltrials.gov NCT00705965 (registered 27th of June, 2008). www.isrctn.com ISRCTN76240576 (registered 27th of March, 2008). |
Databáze: | OpenAIRE |
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