Home > Publications database > Mediation of the Association Between Vascular Risk Factors and Depressive Symptoms by C-Reactive Protein: Longitudinal Evidence from the UK Biobank > print |
001 | 941224 | ||
005 | 20230123101919.0 | ||
024 | 7 | _ | |a 10.31234/osf.io/m8zv4 |2 doi |
024 | 7 | _ | |a 2128/33693 |2 Handle |
037 | _ | _ | |a FZJ-2023-00827 |
100 | 1 | _ | |a Romankiewicz, Lina |0 P:(DE-HGF)0 |b 0 |e Corresponding author |
245 | _ | _ | |a Mediation of the Association Between Vascular Risk Factors and Depressive Symptoms by C-Reactive Protein: Longitudinal Evidence from the UK Biobank |
260 | _ | _ | |c 2022 |
336 | 7 | _ | |a Preprint |b preprint |m preprint |0 PUB:(DE-HGF)25 |s 1674114031_13044 |2 PUB:(DE-HGF) |
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336 | 7 | _ | |a Electronic Article |0 28 |2 EndNote |
336 | 7 | _ | |a preprint |2 DRIVER |
336 | 7 | _ | |a ARTICLE |2 BibTeX |
336 | 7 | _ | |a Output Types/Working Paper |2 DataCite |
520 | _ | _ | |a People with vascular risk factors (VRFs) are at higher risk for depressive symptoms. Given recent findings implicating low-grade systemic inflammation in both vascular and mental health, this study examined the extent to which the VRF–depressive symptom association might be mediated by low-grade systemic inflammation. To this end, we analysed longitudinal data of 9,034 participants from the UK Biobank (mean age = 56.54 years), who took part in three consecutive assessments over the course of about 8 years. Cumulative VRF burden at baseline was defined as the presence of 5 VRFs (hypertension, obesity, hypercholesterolemia, diabetes, and smoking). Low-grade systemic inflammation was assessed using serum-derived C-reactive protein (CRP) and depressive symptoms were measured using the Patient Health Questionnaire-9 (PHQ-9). We performed mediation models using longitudinal data and a path analytic framework, while controlling for age, gender, racial-ethnic background, socioeconomic status, and baseline mood. VRFs at baseline showed a small association with higher depressive symptoms at follow-up (total effect = 0.014, 95% CI [0.007; 0.021]). CRP mediated this association (indirect effect = 0.003, 95% CI [0.001; 0.005]) and accounted for 20.10% of the total effect of VRF burden on depressive symptoms. Exploratory analyses taking a symptom-based approach revealed that mediating pathways pertained to specific depressive symptoms: tiredness and changes in appetite. These results suggest that the small association between VRF burden and depressive symptoms may be partly explained by the inflammation-promoting effects of VRFs, which might promote a specific symptom-profile of depression. |
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700 | 1 | _ | |a Nestler, Steffen |0 P:(DE-HGF)0 |b 2 |
700 | 1 | _ | |a Villringer, Arno |0 P:(DE-HGF)0 |b 3 |
700 | 1 | _ | |a Blöchl, Maria |0 P:(DE-HGF)0 |b 4 |
773 | _ | _ | |a 10.31234/osf.io/m8zv4 |
856 | 4 | _ | |u https://juser.fz-juelich.de/record/941224/files/preprint_romankiewicz_vrfinfdep_v1-1.pdf |y OpenAccess |
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914 | 1 | _ | |y 2022 |
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