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血清血管生成素样蛋白 4 水平及其在脂肪组织中的表达与同卵双胞胎肥胖呈负相关。

Serum angiopoietin-like 4 protein levels and expression in adipose tissue are inversely correlated with obesity in monozygotic twins.

机构信息

National Institute for Health and Welfare, Biomedicum, Helsinki, Finland.

出版信息

J Lipid Res. 2011 Aug;52(8):1575-82. doi: 10.1194/jlr.P015867. Epub 2011 May 19.

DOI:10.1194/jlr.P015867
PMID:21596930
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3137024/
Abstract

Animal studies have suggested that angiopoietin-like 4 (Angptl4) regulates adiposity through central and peripheral mechanisms. The aim of this study was to investigate whether serum concentration and adipose tissue expression of Angptl4 are associated with obesity-related parameters in humans. Altogether, 75 dizygotic (DZ) and 46 monozygotic (MZ) twin pairs were studied, from the FinnTwin12 and FinnTwin16 cohorts. Among the MZ pairs, 21 were discordant for body mass index (BMI) (intra-pair BMI-difference >2.5 kg/m², age 23-33 years). Serum Angptl4 (s-Angptl4) levels were measured by ELISA, and adipose tissue gene expression was analyzed by genome-wide transcript profiling. In MZ twin pairs discordant for BMI, s-Angptl4 and adipose tissue ANGPTL4 mRNA (at-ANGPTL4) levels were significantly decreased (P = 0.04 and P = 0.03, respectively) in obese twins as compared with their nonobese cotwins. In all twins, intra-pair differences in s-Angptl4 levels were inversely correlated with intra-pair differences in BMI (r = -0.27, P = 0.003). In individual MZ twins, at-ANGPTL4 expression was inversely correlated with BMI (r = -0.44, P = 0.001) and positively correlated with at-LIPE (r = 0.24, P = 0.01) and at-ABHD5 (r = 0.41, P = 0.005) expression. Our results demonstrated that variation in Angptl4 concentration was only modestly accounted for by genetic factors and suggest a role for Angptl4 in acquired obesity in humans.

摘要

动物研究表明,血管生成素样 4(Angptl4)通过中枢和外周机制调节脂肪量。本研究旨在探讨血清 Angptl4 浓度和脂肪组织表达与肥胖相关参数在人类中的相关性。总共研究了来自 FinnTwin12 和 FinnTwin16 队列的 75 对异卵双胞胎(DZ)和 46 对同卵双胞胎(MZ)。在 MZ 双胞胎中,21 对 BMI 不一致(同对 BMI 差异>2.5kg/m²,年龄 23-33 岁)。通过 ELISA 测量血清 Angptl4(s-Angptl4)水平,并通过全基因组转录谱分析脂肪组织基因表达。在 BMI 不一致的 MZ 双胞胎中,肥胖双胞胎的 s-Angptl4 和脂肪组织 ANGPTL4 mRNA(at-ANGPTL4)水平显著降低(P=0.04 和 P=0.03)。在所有双胞胎中,s-Angptl4 水平的同对差异与 BMI 的同对差异呈负相关(r=-0.27,P=0.003)。在个体 MZ 双胞胎中,at-ANGPTL4 表达与 BMI 呈负相关(r=-0.44,P=0.001),与 at-LIPE(r=0.24,P=0.01)和 at-ABHD5(r=0.41,P=0.005)表达呈正相关。我们的结果表明,Angptl4 浓度的变异仅由遗传因素适度解释,并表明 Angptl4 在人类获得性肥胖中起作用。

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Podocyte-secreted angiopoietin-like-4 mediates proteinuria in glucocorticoid-sensitive nephrotic syndrome.足细胞分泌的血管生成素样蛋白 4 在糖皮质激素敏感型肾病综合征中的蛋白尿形成中起介导作用。
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