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内脏肥胖调节载脂蛋白 C3 基因变异对肝脂肪含量的影响。

Visceral obesity modulates the impact of apolipoprotein C3 gene variants on liver fat content.

机构信息

Department of Internal Medicine, Division of Endocrinology, Diabetology, Vascular Medicine, Nephrology and Clinical Chemistry, University of Tübingen, Otfried-Müller-Street 10, Tübingen, Germany.

出版信息

Int J Obes (Lond). 2012 Jun;36(6):774-82. doi: 10.1038/ijo.2011.154. Epub 2011 Aug 9.

Abstract

OBJECTIVE

It has not been solved whether subjects carrying the minor alleles of the -455T>C or -482C>T single nucleotide polymorphisms (SNPs) in the apolipoprotein-C3-gene (APOC3) have an increased risk for developing fatty liver and insulin resistance. We investigated the relationships of the SNPs with hepatic APOC3 expression and hypothesized that visceral obesity may modulate the effects of these SNPs on liver fat and insulin sensitivity (IS).

METHODS

APOC3 mRNA expression and triglyceride content were determined in liver biopsies from 50 subjects. In a separate group (N=330) liver fat was measured by (1)H-magnetic resonance spectroscopy. IS was estimated during an oral glucose tolerance test (OGTT) and the euglycemic, hyperinsulinemic clamp (N=222).

RESULTS

APOC3 mRNA correlated positively with triglyceride content in liver biopsies (r=0.29, P=0.036). Carriers of the minor alleles (-455C and -482T) tended to have higher hepatic APOC3 mRNA expression (1.80 (0.45-3.56) vs 0.77 (0.40-1.64), P=0.09), but not higher triglyceride content (P=0.76). In 330 subjects the genotype did not correlate with liver fat (P=0.97) or IS (OGTT: P=0.41; clamp: P=0.99). However, a significant interaction of the genotype with waist circumference in determining liver fat was detected (P=0.02) in which minor allele carriers had higher liver fat only in the lowest tertile of waist circumference (P=0.01). In agreement, during a 9-month lifestyle intervention the minor allele carriers of the SNP -482C>T in the lowest tertile also had less decrease in liver fat (P=0.04).

CONCLUSIONS

APOC3 mRNA expression is increased in fatty liver and is regulated by SNPs in APOC3. The impact of the APOC3 SNPs on fatty liver is small and depends on visceral obesity.

摘要

目的

载脂蛋白 C3 基因(APOC3)-455T>C 或 -482C>T 单核苷酸多态性(SNP)的次要等位基因的个体是否患脂肪肝和胰岛素抵抗的风险增加,目前尚未解决。我们研究了这些 SNP 与肝 APOC3 表达的关系,并假设内脏肥胖可能调节这些 SNP 对肝脂肪和胰岛素敏感性(IS)的影响。

方法

在 50 例肝活检标本中测定 APOC3mRNA 表达和甘油三酯含量。在另一组(N=330)中,通过(1)H 磁共振波谱法测量肝脂肪。在口服葡萄糖耐量试验(OGTT)和正葡萄糖、高胰岛素钳夹(N=222)期间估计 IS。

结果

APOC3mRNA 与肝活检中甘油三酯含量呈正相关(r=0.29,P=0.036)。携带次要等位基因(-455C 和 -482T)的个体肝 APOC3mRNA 表达水平较高(1.80(0.45-3.56)比 0.77(0.40-1.64),P=0.09),但甘油三酯含量无差异(P=0.76)。在 330 例患者中,基因型与肝脂肪(P=0.97)或 IS(OGTT:P=0.41;钳夹:P=0.99)无关。然而,在确定肝脂肪时,基因型与腰围的交互作用显著(P=0.02),其中仅在腰围最低三分位的次要等位基因携带者肝脂肪更高(P=0.01)。一致的是,在 9 个月的生活方式干预中,SNP-482C>T 的最小等位基因携带者的肝脂肪减少也较少(P=0.04)。

结论

APOC3mRNA 表达在脂肪肝中增加,并受 APOC3 的 SNP 调节。APOC3SNP 对脂肪肝的影响较小,且取决于内脏肥胖。

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