4.6 Article

Increased LDL-cholesterol level is associated with deterioration of renal function in males

Journal

CLINICAL KIDNEY JOURNAL
Volume 15, Issue 10, Pages 1888-1895

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/ckj/sfac111

Keywords

chronic kidney disease; dyslipidemia; high-density lipoprotein cholesterol; low-density lipoprotein-cholesterol

Funding

  1. Grants for Education and Research
  2. Sapporo Medical University
  3. Japan Society for the Promotion of Science [19K08708, 20K08913]
  4. Grants-in-Aid for Scientific Research [19K08708, 20K08913] Funding Source: KAKEN

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This study examines the relationship between serum lipid levels and the time course of renal function in a cohort of healthy subjects. The findings suggest that a high LDL-C level may be a risk factor for new-onset chronic kidney disease in apparently healthy males.
Background Relationships between levels of serum lipid fractions and the time course of renal function are discrepant in the literature. Here we examined this issue by analyses of healthy subjects in a cohort. Methods Of all subjects who received health examinations at Keijinkai Maruyama Clinic, Sapporo in 2006, subjects with hypertension, diabetes mellitus or chronic kidney disease (CKD) and those taking medication for dyslipidemia were excluded and a total of 5586 subjects (male/female: 3563/2023, mean age: 43 +/- 8 years) were followed for 10 years. Results Linear mixed effect models showed that baseline low-density lipoprotein-cholesterol (LDL-C) level was negatively associated with estimated glomerular filtration rate (eGFR) during the 10-year follow-up period after adjustment for confounders. Interactions between the follow-up year and baseline level of LDL-C or high-density lipoprotein-cholesterol (HDL-C) for eGFR values during the follow-up period were significant in males but not in females. There were no significant interactions for eGFR between the follow-up year and baseline levels of total cholesterol, triglycerides, or HDL-C/triglycerides ratio. During the follow-up period, 346 males and 223 females developed CKD. When male subjects were divided into subgroups according to tertiles of baseline levels of LDL-C, the adjusted risk for CKD in the third tertial group was significantly higher than that in the first tertile group as a reference [hazard ratio (95% confidence interval): 1.39 (1.02-1.90), P = .035]. Such a difference was not observed for LDL-C tertiles in females or HDL-C tertiles in both sexes. Conclusions A high LDL-C level may be a risk factor for new-onset CKD in apparently healthy males.

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