Department of Medicine, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Minerva Foundation Institute for Medical Research, Helsinki, Finland.
J Clin Endocrinol Metab. 2021 Jan 1;106(1):e300-e315. doi: 10.1210/clinem/dgaa729.
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.
To study whether PNPLA3-I148M confers an antihyperlipidemic effect in insulin-resistant patients.
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.
Tertiary referral center.
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).
Nuclear magnetic resonance profiling of plasma lipids, lipoprotein particle subclasses and their composition.
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.
PNPLA3-I148M confers an antiatherogenic plasma lipid profile particularly in insulin-resistant individuals.
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。
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。
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。
三级转诊中心。
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。
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。
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。
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。