Abstract

Previous studies suggest lower concentrations of total and high-density lipoprotein (HDL) cholesterol to be predictive of depression. We therefore investigated the relationship of lipids and lipoprotein distribution with elevated depressive symptoms (EDS) in healthy men and women from the Multi-Ethnic Study of Atherosclerosis (MESA). Participants were followed up over a 9.5-year period. EDS were defined as a Center for Epidemiological Studies Depression (CES-D) score ⩾16 and/or use of antidepressant drugs. Lipoprotein distribution was determined from plasma using nuclear magnetic resonance spectroscopy. Among 4938 MESA participants (mean age=62 years) without EDS at baseline, 1178 (23.9%) developed EDS during follow-up. In multivariable Cox regression analyses, lower total, low-density lipoprotein (LDL) and non-HDL cholesterol concentrations at baseline were associated with incident EDS over 9.5 years (hazards ratio (HR)=1.11–1.12 per s.d. decrease, all P<0.01), after adjusting for demographic factors, traditional risk factors including LDL cholesterol, HDL cholesterol and triglycerides. Lipoprotein particle subclasses and sizes were not associated with incident EDS. Among participants without EDS at both baseline and visit 3, a smaller increase in total or non-HDL cholesterol between these visits was associated with lower risk of incident EDS after visit 3 (HR=0.88–0.90 per s.d. decrease, P<0.05). Lower baseline concentrations of total, LDL and non-HDL cholesterol were significantly associated with a higher risk of incident EDS. However, a short-term increase in cholesterol concentrations did not help to reduce the risk of EDS. Further studies are needed to replicate our findings in cohorts with younger participants.

Highlights

  • Previous studies have suggested a possible relationship between dyslipidemia and depression

  • The characteristics of the 4938 Multi-Ethnic Study of Atherosclerosis (MESA)-included participants and the 1876 excluded participants are shown in Supplementary Table S2

  • The association of lower concentrations of total cholesterol (HR (95% confidence interval (CI)) = 1.11 (1.03–1.19) per s.d. decrease, P = 0.004), low-density lipoprotein (LDL) cholesterol (HR = 1.10 (1.03–1.17) per s.d. decrease, P = 0.004), non-high-density lipoprotein (HDL) cholesterol (HR = 1.11 (1.03–1.19) per s.d. decrease, P = 0.004), total/HDL cholesterol ratio (HR = 1.11 (1.00–1.22) per s.d. decrease, P = 0.04) and LDL/HDL cholesterol ratio (HR = 1.01 (1.01–1.19) per s.d. decrease, P = 0.02) with a higher incident elevated depressive symptoms (EDS) risk remained significant after further adjustment for large high-density lipoprotein particle (HDL-P) concentration

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Summary

Introduction

Previous studies have suggested a possible relationship between dyslipidemia and depression. In a study of 29 133 men aged 50–69 years in Finland with a follow-up period of 5–8 years, a low serum total cholesterol concentration at baseline was associated with major depression and death from suicide.[1] this study assessed total and high-density lipoprotein (HDL) cholesterol concentrations only. As the precise link between lipid profile and depression is not well established, longitudinal studies in other settings are needed to strengthen the evidence for a causal relationship. It is not known whether there is any difference in such a relationship across subgroups of subject characteristics, especially race/ ethnicity, sex and baseline cholesterol concentration

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