Suppr超能文献

载脂蛋白基因 PNPLA3-I148M 变异赋予胰岛素抵抗患者抗动脉粥样硬化的脂质谱。

The PNPLA3-I148M Variant Confers an Antiatherogenic Lipid Profile in Insulin-resistant Patients.

机构信息

Department of Medicine, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.

Minerva Foundation Institute for Medical Research, Helsinki, Finland.

出版信息

J Clin Endocrinol Metab. 2021 Jan 1;106(1):e300-e315. doi: 10.1210/clinem/dgaa729.

Abstract

CONTEXT

The I148M (rs738409-G) variant in PNPLA3 increases liver fat content but may be protective against cardiovascular disease. Insulin resistance (IR) amplifies the effect of PNPLA3-I148M on liver fat.

OBJECTIVE

To study whether PNPLA3-I148M confers an antihyperlipidemic effect in insulin-resistant patients.

DESIGN

Cross-sectional study comparing the impact of PNPLA3-I148M on plasma lipids and lipoproteins in 2 cohorts, both divided into groups based on rs738409-G allele carrier status and median HOMA-IR.

SETTING

Tertiary referral center.

PATIENTS

A total of 298 obese patients who underwent a liver biopsy during bariatric surgery (bariatric cohort: age 49 ± 9 years, body mass index [BMI] 43.2 ± 6.8 kg/m2), and 345 less obese volunteers in whom liver fat was measured by proton magnetic resonance spectroscopy (nonbariatric cohort: age 45 ± 14 years, BMI 29.7 ± 5.7 kg/m2).

MAIN OUTCOME MEASURES

Nuclear magnetic resonance profiling of plasma lipids, lipoprotein particle subclasses and their composition.

RESULTS

In both cohorts, individuals carrying the PNPLA3-I148M variant had significantly higher liver fat content than noncarriers. In insulin-resistant and homozygous carriers, PNPLA3-I148M exerted a distinct antihyperlipidemic effect with decreased very-low-density lipoprotein (VLDL) and low-density lipoprotein (LDL) particles and their constituents, and increased high-density lipoprotein particles and their constituents, compared with noncarriers. VLDL particles were smaller and LDL particles larger in PNPLA3-I148M carriers. These changes were geometrically opposite to those due to IR. PNPLA3-I148M did not have a measurable effect in patients with lower IR, and its effect was smaller albeit still significant in the less obese than in the obese cohort.

CONCLUSIONS

PNPLA3-I148M confers an antiatherogenic plasma lipid profile particularly in insulin-resistant individuals.

摘要

背景

载脂蛋白 PLA3 基因的 I148M(rs738409-G) 变体可增加肝脏脂肪含量,但可能对心血管疾病具有保护作用。胰岛素抵抗(IR)会放大载脂蛋白 PLA3 基因 I148M 对肝脏脂肪的影响。

目的

研究载脂蛋白 PLA3 基因 I148M 是否在胰岛素抵抗患者中具有抗高脂血症作用。

设计

比较了 2 个队列中载脂蛋白 PLA3 基因 I148M 对血浆脂质和脂蛋白的影响,这 2 个队列均根据 rs738409-G 等位基因携带状态和中位 HOMA-IR 进行分组。

地点

三级转诊中心。

患者

共纳入 298 例因减重手术而行肝活检的肥胖患者(减重组:年龄 49±9 岁,体重指数 [BMI]43.2±6.8kg/m2)和 345 例非肥胖志愿者,他们的肝脂肪通过质子磁共振波谱(非减重组:年龄 45±14 岁,BMI29.7±5.7kg/m2)进行测量。

主要观察指标

对血浆脂质、脂蛋白颗粒亚类及其组成进行核磁共振谱分析。

结果

在这两个队列中,携带载脂蛋白 PLA3 基因 I148M 变体的个体的肝脏脂肪含量明显高于非携带者。在胰岛素抵抗和纯合子携带者中,与非携带者相比,载脂蛋白 PLA3 基因 I148M 具有明显的抗高脂血症作用,表现为极低密度脂蛋白(VLDL)和低密度脂蛋白(LDL)颗粒及其成分减少,高密度脂蛋白颗粒及其成分增加。载脂蛋白 PLA3 基因 I148M 携带者的 VLDL 颗粒更小,LDL 颗粒更大。这些变化与 IR 引起的变化在几何形状上相反。在 IR 较低的患者中,载脂蛋白 PLA3 基因 I148M 没有可测量的作用,而在较不肥胖的患者中,其作用虽小但仍有统计学意义。

结论

载脂蛋白 PLA3 基因 I148M 赋予了一种抗动脉粥样硬化的血浆脂质谱,特别是在胰岛素抵抗个体中。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验