Table 6. Multivariable adjusted associations of somatic versus cognitive symptom dimensions of depression.
Dependent variables | Somatic symptom subscale (0–12) | Cognitive symptom subscale (0–15) | ||
Logistic Regression models,OR (95% CI), p | Linear Regressionmodels, β-estimate(95% CI), p | Logistic Regressionmodels, OR (95% CI), p | Linear Regression models, β-estimate (95% CI), p | |
CHD | 1.25 (1.14, 1.39), <0.0001 | 1.02 (0.92, 1.13), 0.68 | ||
History of MI | 1.22 (1.09, 1.37), <0.001 | 0.99 (0.88, 1.13), 0.92 | ||
Family history of MI# | 1.08 (1.02, 1.14), 0.0055 | 1.02 (0.96, 1.07), 0.51 | ||
Diabetes | 0.97 (0.89, 1.06), 0.53 | 1.05 (0.96, 1.15), 0.29 | ||
Hypertension | 1.01 (0.96, 1.06), 0.77 | 0.96 (0.91, 1.00), 0.064 | ||
Dyslipidemia | 1.09 (1.04, 1.14), <0.001 | 0.99 (0.94, 1.04), 0.62 | ||
Smoking (current) | 1.06 (1.01, 1.12), 0.019 | 1.00 (0.95, 1.06), 0.92 | ||
Obesity (BMI ≥30) | 1.15 (1.09, 1.21), <0.0001 | 0.93 (0.88, 0.98), 0.0035 | ||
Physical Activity score (continuous) | 36.05 (−38.25, 110.36), 0.34 | −27.94 (−103.68, 47.80), 0.47 | ||
Medical history of depression | 1.22 (1.15, 1.30), <0.0001 | 1.39 (1.30, 1.47), <0.0001 | ||
Type D personality | 1.13 (1.08, 1.19), <0.0001 | 1.51 (1.43, 1.60), <0.0001 | ||
Biomarkers * | ||||
CRP≥3 mg/dl (yes vs. no) | 1.02 (0.96, 1.09), 0.44 | 0.98 (0.92, 1.04), 0.45 | ||
IL-18, pg/ml | 0.0061 (−0.0024, 0.015), 0.16 | −0.0056 (−0.014, 0.0030), 0.20 | ||
IL-1-ra, pg/ml | 0.00067 (−0.0090, 0.010), 0.89 | 0.0021 (−0.0077, 0.012), 0.68 | ||
Albumin, mg/l | −0.039 (−0.11, 0.032), 0.28 | −0.011 (−0.082, 0.061), 0.77 | ||
Fibrinogen, mg/dl | 0.0013 (−0.0027, 0.0053), 0.53 | −0.0033 (−0.0074, 0.00079), 0.11 | ||
NT-proBNP, pg/ml | 0.087 (−0.015, 0.032), 0.47 | −0.012 (−0.036, 0.012), 0.32 |
Adjusted for age, sex, dyslipidemia, current smoking, diabetes, hypertension, Body mass index, 5 kg/m2, Activity score (Q1–Q4), FH of MI and socioeconomic status (3–27). The predictors (somatic and cognitive subscale) were entered together in each regression analyses.
Exclusion of subjects with CHD attenuates the relationship of the somatic symptom scale with FH of MI only slightly OR 1.06 (1.00–1.12), p = 0.0361.
For analysis of CRP, IL-18, IL-1-ra, and Albumin subjects with a self reported influenza infection, common cold or other inflammatory diseases during the last week before examination or CRP≥10 mg/dl are excluded. All biomarkers except for Albumin and CRP were log transformed.