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Journal of Zhejiang University SCIENCE B

ISSN 1673-1581(Print), 1862-1783(Online), Monthly

Activity of metalloproteinases and adiponectin in obese patients—a possible factor of incisional hernias after bariatric procedures

Abstract: Purpose: Metalloproteinases are a key component of the pathogenesis of abdominal hernias. Obesity is considered a risk factor in herniogenesis and hernia recurrence. The aim of this study was to evaluate the serum concentrations of metalloproteinase-2 (MMP-2), MMP-9, MMP-13, and adiponectin in morbidly obese and non-overweight controls. Materials and methods: The participants were recruited from among patients undergoing bariatric and non-bariatric surgery and divided into two groups: I (body mass index (BMI)≥35 kg/m2, n=40) and II (BMI<25 kg/m2, n=30). Serum concentrations of MMP-2, MMP-9, MMP-13, and adiponectin were measured using enzyme-linked immunosorbent assay (ELISA). Results: A statistically significant difference between groups was observed for MMP-2 concentration. The median MMP-9 concentration was higher in the obese group, but the difference was not statistically significant. Median MMP-13 concentrations did not differ between groups. Serum adiponectin concentration was insignificantly higher in the non-obese group. Conclusions: The elevated serum MMP-2 and MMP-9 concentrations in obese individuals may be related to the higher incidence of incisional hernias in this population.

Key words: Metalloproteinase; Adiponectin; Obesity; Incisional hernia

Chinese Summary  <19> 肥胖患者体内金属蛋白酶和脂联素的活性-- 肥胖手术后造成切口疝的可能因素

目的:主要研究病态肥胖患者与正常人血清中金属蛋白酶2(MMP-2)、MMP-9、MMP-13和脂联素的浓度.
创新点:建立血清中MMP-2、MMP-9、MMP-13和脂联素的浓度与肥胖和切口疝的关系.
方法:参与实验的人员为进行肥胖手术的患者和不进行肥胖手术的患者,并将他们分为两组:I(体重指数(BMI)≥35 kg/m2,n=40)和II(BMI<25 kg/m2,n=30),并使用酶联免疫吸附实验测定受试人员体内血清中MMP-2、MMP-9、MMP-13和脂联素的浓度.
结论:MMP-2的浓度在肥胖组中更高,且在两组血清中有显著性差异.虽然MMP-9的浓度在肥胖组中更高,但是两组之间没有显著性差异.MMP-13在两组间没有差异.血清中脂联素的浓度在非肥胖组更高,但无显著性差异.因此,血清中MMP-2和MMP-9的浓度在肥胖人群中与更高的切口疝发病率有关.

关键词组:金属蛋白酶;脂联素;肥胖症;切口疝


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DOI:

10.1631/jzus.B1600383

CLC number:

R656.2

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On-line Access:

2018-01-11

Received:

2016-11-23

Revision Accepted:

2017-03-17

Crosschecked:

2017-12-18

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