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瘦素-黑皮质素途径变异与肥胖症患者胃排空。

Leptin-Melanocortin pathway variants and gastric emptying in patients with obesity.

机构信息

Precision Medicine for Obesity Program, Division of Gastroenterology and Hepatology, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.

Division of Epidemiology, Department of Quantitative Health Sciences, Mayo Clinic, Rochester, Minnesota, USA.

出版信息

Neurogastroenterol Motil. 2024 May;36(5):e14764. doi: 10.1111/nmo.14764. Epub 2024 Feb 15.

Abstract

BACKGROUND

Accelerated gastric emptying (GE) is a trait seen in obesity. Mutations in the hypothalamic leptin-melanocortin 4 receptor (Leptin-MC4R) pathway have been associated with obesity. We sought to investigate the association of leptin-MC4R pathway variants and GE in patients with obesity.

METHODS

This is a cross-sectional study of patients with a history of severe obesity that were genotyped and completed a GE test by scintigraphy. We evaluated the percentage of GE (GE %) at 2 and 4 h between both groups using ANCOVA with weight and sex as covariates. We subdivide patients into carriers based on the location of the identified variants (i.e., upstream or downstream of the Leptin-MC4R pathway) and compared them with noncarriers using ANOVA. Results are presented as mean and standard deviation (± SD).

KEY RESULTS

A total of 95 patients; nine carriers (67% females; 39.78 ± 12.33 years; BMI: 49.14 ± 12.96 kg/m2) and 86 noncarriers (87% female; 49.98 ± 13.74 years; BMI: 40.75 ± 6.29 kg/m2) were included. At 2 and 4 h, carriers had a delayed GE when compared noncarriers (p = 0.03 and p = 0.005, respectively). In carriers, when compared upstream carriers vs. downstream carriers vs. noncarriers by location there was a significant difference in GE among groups at 2 h and at 4 h (p = 0.02 and p = 0.01, respectively).

CONCLUSIONS & INFERENCES: Carriers of heterozygous variants in the Leptin-MC4R pathway had a delayed GE compared to noncarriers. These findings point the important relationship between the Leptin-MC4R pathway and gastric motility.

摘要

背景

加速胃排空(GE)是肥胖症的一种特征。瘦素-黑素皮质素 4 受体(Leptin-MC4R)通路中的突变与肥胖有关。我们试图研究瘦素-MC4R 通路变异与肥胖患者 GE 的关系。

方法

这是一项对有严重肥胖病史的患者进行的横断面研究,对其进行基因分型并通过闪烁扫描法进行 GE 测试。我们使用协方差分析(ANCOVA)评估两组患者在 2 小时和 4 小时时的 GE 百分比(GE%),体重和性别作为协变量。我们根据鉴定出的变异位置(即瘦素-MC4R 通路的上游或下游)将患者分为携带者,并与非携带者进行比较。结果以平均值和标准差(±SD)表示。

主要结果

共有 95 名患者;9 名携带者(67%为女性;39.78±12.33 岁;BMI:49.14±12.96kg/m2)和 86 名非携带者(87%为女性;49.98±13.74 岁;BMI:40.75±6.29kg/m2)。在 2 小时和 4 小时时,与非携带者相比,携带者的 GE 延迟(p=0.03 和 p=0.005)。在携带者中,根据变异位置将上游携带者与下游携带者与非携带者进行比较时,在 2 小时和 4 小时时,各组之间的 GE 存在显著差异(p=0.02 和 p=0.01)。

结论

Leptin-MC4R 通路杂合变异携带者的 GE 较非携带者延迟。这些发现指出了 Leptin-MC4R 通路与胃动力之间的重要关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b14/11042991/ceea6d0e2514/nihms-1966582-f0002.jpg

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