Journal of Southern Medical University ›› 2015, Vol. 35 ›› Issue (07): 1019-.
Previous Articles Next Articles
Online:
Published:
Abstract: Objective To investigate the association of serum pigment epithelium-derived factor (PEDF) level andpolymorphisms in PEDF gene promoter region -358G→A with non-alcoholic fatty liver disease (NAFLD) in patients with type2 diabetes mellitus (T2DM) of Han Nationality in Fujian Province. Methods A total of 282 T2DM patients with NAFLD (DM1group) and 170 age- and gender-matched T2DM patients without NAFLD (DM2 group) were examined for PEDF geneSNP-358G→A polymorphisms using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP).Serum pigment epithelium-derived factor(PEDF) level, fasting plasma glucose (FPG), fasting insulin (FINS) and glycosylatedhemoglobin (HbA1c) were also measured. Results The patients in DM1 group showed a significantly higher mean level ofserum PEDF than those in DM2 group (P<0.05). Logistic regression analysis revealed that PEDF level was an independent riskfactor for NAFLD in T2DM. The frequencies of PEDF gene -358G→A genotypes (GG, GA, and AA) and alleles (G/A) differedsignificanly between DM1 and DM2 groups (P<0.05). In terms of PEDF gene SNP -358G→A alleles, the GA genotype carriershad a 2.032 times higher risk of developing NAFLD compared with the GG genotype carriers, and the risk increased to 2.068times in the carriers of the A allele (GA and AA genotypes; P<0.05). Conclusion Serum PEDF level is an independent risk factorof NAFLD in T2DM. Elevated serum PEDF level is a protective factor against insulin resistance. In T2DM patients, PEDF genepromoter region -358G→A polymorphism is associated with NAFLD, and the A allele contributes to an increased risk ofNAFLD.
0 / / Recommend
Add to citation manager EndNote|Ris|BibTeX
URL: https://www.j-smu.com/EN/
https://www.j-smu.com/EN/Y2015/V35/I07/1019