Published online Jul 16, 2024. doi: 10.12998/wjcc.v12.i20.4256
Revised: May 14, 2024
Accepted: May 15, 2024
Published online: July 16, 2024
Processing time: 67 Days and 19.6 Hours
Dyslipidemia is a common complication in patients with diabetes mellitus (DM) that increases the risk of cardiovascular disease. Genetic polymorphisms have been implicated in the development of dyslipidemia.
To investigate the association between polymorphisms of candidate genes involved in lipid metabolism and dyslipidemia in Chinese patients with DM.
A cross-sectional study was conducted on 1098 Chinese patients with DM re
The study population consisted of 578 males (52.6%) and 520 females (47.4%), with a mean age of 58.4 ± 12.2 years. The prevalence of dyslipidemia was 64.8%. Significant associations were found between dyslipidemia and the APOE rs7412 T/T, APOE rs429358 C/C, LPL rs328 G/G, and CETP rs708272 G/G genotypes after adjusting for covariates. Subgroup analyses showed generally consistent associations across subgroups, although some variations in effect sizes were observed.
This study identified significant associations between genetic polymorphisms of APOE, LPL, and CETP genes and dyslipidemia in Chinese patients with DM.
Core Tip: Genetic polymorphisms of APOE, LPL, and CETP genes are significantly associated with dyslipidemia in Chinese patients with diabetes mellitus (DM). Understanding these associations can provide valuable insights into personalized management strategies for dyslipidemia in this population, emphasizing the importance of genetic factors in lipid metabolism and cardiovascular risk assessment. Subgroup analyses further support the robustness of these associations across different patient groups, highlighting the potential for targeted interventions based on genetic profiles in the management of dyslipidemia in Chinese individuals with DM.
