Why the study?
The etiology of depression remains poorly understood, and previous study findings regarding the association of blood lipid levels with depression and suicide have been mixed.
Do genetically predicted blood lipid levels causally affect depression phenotypes?
Observational (n=668,936)
Yes
Do genetically predicted blood lipid levels causally affect depression phenotypes?
Mendelian randomization suggests a causal relationship between elevated triglycerides and increased risk of depressive symptoms and self-harm.
Supports causal TG-depression link via MR; hypothesis-generating for lipid trials before practice change.
BACKGROUND: The etiology of depression remains poorly understood. Changes in blood lipid levels were reported to be associated with depression and suicide, however study findings were mixed. METHODS: We performed a two-sample Mendelian randomisation (MR) analysis to investigate the causal relationship between blood lipids and depression phenotypes, based on large-scale GWAS summary statistics (N = 188 577/480 359 for lipid/depression traits respectively). Five depression-related phenotypes were included, namely major depression (MD; from PGC), depressive symptoms (DS; from SSGAC), longest duration and number of episodes of low mood, and history of deliberate self-harm (DSH)/suicide (from UK Biobank). MR was conducted with inverse-variance weighted (MR-IVW), Egger and Generalised Summary-data-based MR (GSMR) methods. RESULTS: There was consistent evidence that triglyceride (TG) is causally associated with DS (MR-IVW β for one-s.d. increase in TG = 0.0346, 95% CI 0.0114-0.0578), supported by MR-IVW and GSMR and multiple r2 clumping thresholds. We also observed relatively consistent associations of TG with DSH/suicide (MR-Egger OR = 2.514, CI 1.579-4.003). There was moderate evidence for positive associations of TG with MD and the number of episodes of low mood. For HDL-c, we observed moderate evidence for causal associations with DS and MD. LDL-c and TC did not show robust causal relationships with depression phenotypes, except for weak evidence that LDL-c is inversely related to DSH/suicide. We did not detect significant associations when depression phenotypes were treated as exposures. CONCLUSIONS: This study provides evidence to a causal relationship between TG, and to a lesser extent, altered cholesterol levels with depression phenotypes. Further studies on its mechanistic basis and the effects of lipid-lowering therapies are warranted.
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So et al. (2020) conducted an observational in Depression phenotypes (n=668,936). Blood lipids (Triglycerides, HDL-c, LDL-c, Total Cholesterol) was evaluated on Depressive symptoms (DS) (β 0.0346, 95% CI 0.0114-0.0578).
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