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作为妊娠高血压标志物的zonulin:一项病例对照研究。

Zonulin as marker of pregnancy induced hypertension: a case control study.

作者信息

Bawah Ahmed Tijani, Tornyi Henry, Seini Mohammed Mustapha, Ngambire Lincoln Toamsoma, Yeboah Francis Agyemang

机构信息

1Department of Medical Laboratory Sciences, University of Health and Allied Science, PMB 31, Ho, Ghana.

2Department of Molecular Medicine, Kwame Nkrumah University Science and Technology, Kumasi, Ghana.

出版信息

Clin Hypertens. 2020 Apr 15;26:7. doi: 10.1186/s40885-020-00139-x. eCollection 2020.

DOI:10.1186/s40885-020-00139-x
PMID:32313692
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7158010/
Abstract

BACKGROUND

Zonulin has been implicated in many metabolic disorders including hypertension and obesity. However, there is insufficient information about the involvement of zonulin in pregnancy induced hypertension (PIH) which comprises preeclampsia (PE) and gestational hypertension (GH). This study was therefore aimed at finding the level of this biochemical marker of regulation of tight junctions among women with PIH.

METHODS

A total of 88 women with PIH and 60 age and body mass index (BMI) matched healthy pregnant women controls were enrolled. Blood pressure at 11-13 weeks and after 20 weeks of gestation, body mass index (BMI) in addition to serum Zonulin levels and lipid profile were compared between the groups. Student's t-test was used for comparisons of the mean between the two groups. Correlation analyses were performed using Pearson's correlation and binary logistic regression was used to evaluate the factors associated with PIH.

RESULTS

Zonulin level was significantly higher in the participants with PIH as compared to the normal pregnant controls 56.81 ± 7.72 ng/ml vs 40.4 ± 8.60 ng/ml  < 0.0001 and had strong positive correlation with PIH (OR = 1.805; CI1.139-1.275; p < 0.0001). However, the association between first trimester lipids and PIH was weak.

CONCLUSION

The results showed a strong positive correlation between zonulin and PIH, thus changes in intestinal permeability occur in early stages of pregnancy and may be involved in the pathogenesis of PIH.

摘要

背景

闭合蛋白与包括高血压和肥胖症在内的多种代谢紊乱有关。然而,关于闭合蛋白在包括先兆子痫(PE)和妊娠期高血压(GH)的妊娠高血压疾病(PIH)中的作用,目前信息不足。因此,本研究旨在确定这种紧密连接调节生化标志物在PIH女性中的水平。

方法

共纳入88例PIH女性和60例年龄及体重指数(BMI)匹配的健康孕妇作为对照。比较两组在妊娠11 - 13周和20周后的血压、BMI、血清闭合蛋白水平及血脂谱。采用学生t检验比较两组均值。使用Pearson相关性进行相关分析,并采用二元逻辑回归评估与PIH相关的因素。

结果

与正常妊娠对照组相比,PIH参与者的闭合蛋白水平显著更高(56.81±7.72 ng/ml对40.4±8.60 ng/ml,<0.0001),且与PIH呈强正相关(OR = 1.805;CI 1.139 - 1.275;p < 0.0001)。然而,孕早期血脂与PIH之间的关联较弱。

结论

结果显示闭合蛋白与PIH之间存在强正相关,因此肠道通透性的变化发生在妊娠早期,可能参与了PIH的发病机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a54/7158010/14b32ec1cbce/40885_2020_139_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a54/7158010/abf1dabfe71c/40885_2020_139_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a54/7158010/14b32ec1cbce/40885_2020_139_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a54/7158010/abf1dabfe71c/40885_2020_139_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a54/7158010/14b32ec1cbce/40885_2020_139_Fig2_HTML.jpg

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本文引用的文献

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Front Cell Infect Microbiol. 2019 Jun 26;9:224. doi: 10.3389/fcimb.2019.00224. eCollection 2019.
2
Adiposity and hyperleptinemia during the first trimester among pregnant women with preeclampsia.先兆子痫孕妇孕早期的肥胖及高瘦素血症。
Int J Womens Health. 2017 Jun 16;9:449-454. doi: 10.2147/IJWH.S134088. eCollection 2017.
3
Increased intestinal permeability, measured by serum zonulin, is associated with metabolic risk markers in overweight pregnant women.
通过血清连蛋白测定的肠道通透性增加与超重孕妇的代谢风险标志物相关。
Metabolism. 2017 Apr;69:43-50. doi: 10.1016/j.metabol.2016.12.015. Epub 2017 Jan 4.
4
Higher Levels of Serum Zonulin May Rather Be Associated with Increased Risk of Obesity and Hyperlipidemia, Than with Gastrointestinal Symptoms or Disease Manifestations.血清中较高水平的zonulin可能与肥胖和高脂血症风险增加有关,而非与胃肠道症状或疾病表现有关。
Int J Mol Sci. 2017 Mar 8;18(3):582. doi: 10.3390/ijms18030582.
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Hypertension-Linked Pathophysiological Alterations in the Gut.肠道中与高血压相关的病理生理改变。
Circ Res. 2017 Jan 20;120(2):312-323. doi: 10.1161/CIRCRESAHA.116.309006. Epub 2016 Oct 31.
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