Journal Article Ppublish
PubMed: 39491271 DOI: 10.1080/0886022X.2024.2420841
Lipid metabolism disorders and albuminuria risk: insights from National Health and Nutrition Examination Survey 2001-2018 and Mendelian randomization analyses.
Ren Fail 46(2):2420841
Authors: Yangyang Wang, Sen Li
Affiliations
- Second Medical College of Wenzhou Medical University, Wenzhou, China.
- School of Basic Medical Sciences, Wenzhou Medical University, Wenzhou, China.
Abstract
BACKGROUND
Previous studies have revealed an underlying connection between abnormal lipid metabolism and albuminuria. We aim to investigate the causal relationship between lipid metabolism disorders and the risk of albuminuria from both a population and genetic perspective.
METHODS
A cross-sectional study was conducted by using data from the National Health and Nutrition Examination Survey (NHANES) 2001-2018. Multivariable-adjusted logistic regression, subgroup analysis, interaction tests and restricted cubic spline (RCS) were employed statistically. Mendelian randomization (MR) analysis was performed to validate the causal relationship between exposure and outcome to mitigate confounding factors and reverse causation interference.
RESULTS
After adjusting for confounders, HDL levels (1.03-2.07 nmol/L) were associated with a reduced risk of albuminuria. In contrast, elevated cholesterol levels (>6.2 nmol/L) and triglyceride levels (>2.3 nmol/L) were associated with an increased risk of albuminuria. Serum triglyceride concentration emerged as a potential risk factor for albuminuria. In MR analysis, a reduced risk of albuminuria was associated with serum total HDL level (IVW: OR = 0.91, 95% CI = 0.86-0.97,  = 0.002). In contrast, cholesterol esters in medium VLDL (IVW: OR = 1.05, 95% CI = 1.00-1.10,  = 0.032), chylomicrons and extremely large VLDL (IVW: OR = 1.08, 95% CI = 1.03-1.14,  = 0.003), and triglycerides (IVW: OR = 1.14, 95% CI = 1.09-1.19,  < 0.001) were associated with an increased risk of albuminuria.
CONCLUSION
A causal relationship exists between serum lipid metabolism disorder and albuminuria risk. Further validation of additional blood lipid metabolism biomarkers is imperative for future studies.
MeSH
Serum, Albuminuria, Lipid Metabolism Disorders, Uremia, Cholesterol, Random Allocation, Triglycerides, Acute Kidney Injury