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The lncRNA MALAT1 rs619586 G Variant Confers Decreased Susceptibility to Recurrent Miscarriage

Cardiovascula disease and recurrent miscarriage have shared risk factors, and some cardiovascular disease-related candidate genes have been confirmed to be associated with recurrent miscarriage. Metastasis-associated lung adenocarcinoma transcript 1 (MALAT1) is a long non-coding RNA (lncRNA) that is...

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Autores principales: Che, Di, Yang, Yanfang, Xu, Yufen, Fang, Zhenzhen, Pi, Lei, Fu, LanYan, Zhou, Huazhong, Tan, Yaqian, Lu, Zhaoliang, Li, Li, Liang, Qihua, Xuan, Qingshan, Gu, Xiaoqiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6465954/
https://www.ncbi.nlm.nih.gov/pubmed/31024342
http://dx.doi.org/10.3389/fphys.2019.00385
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author Che, Di
Yang, Yanfang
Xu, Yufen
Fang, Zhenzhen
Pi, Lei
Fu, LanYan
Zhou, Huazhong
Tan, Yaqian
Lu, Zhaoliang
Li, Li
Liang, Qihua
Xuan, Qingshan
Gu, Xiaoqiong
author_facet Che, Di
Yang, Yanfang
Xu, Yufen
Fang, Zhenzhen
Pi, Lei
Fu, LanYan
Zhou, Huazhong
Tan, Yaqian
Lu, Zhaoliang
Li, Li
Liang, Qihua
Xuan, Qingshan
Gu, Xiaoqiong
author_sort Che, Di
collection PubMed
description Cardiovascula disease and recurrent miscarriage have shared risk factors, and some cardiovascular disease-related candidate genes have been confirmed to be associated with recurrent miscarriage. Metastasis-associated lung adenocarcinoma transcript 1 (MALAT1) is a long non-coding RNA (lncRNA) that is considered to be associated with susceptibility to cardiovascular disease. However, whether lncRNA MALAT1 polymorphisms are related to recurrent miscarriage susceptibility is unclear. We genotyped three lncRNA MALAT1 polymorphisms (rs591291, rs619586, and rs3200401) in 284 patients and 392 controls using TaqMan methods. Logistic regression was used to evaluate the odds ratios (ORs) and 95% confidence intervals (CIs) adjusted for age. Our results showed that the rs619586 G variant had protective effects against recurrent miscarriage (AG vs. AA: adjusted OR = 0.670, 95% CI = 0.457–0.982, p = 0.040; GG vs. AA: adjusted OR = 0.278, 95% CI = 0.079–0.975, p = 0.046; GG/AG vs. AA adjusted OR = 0.621, 95% CI = 0.429–0.900, p = 0.012). In a combined analyses of protective genotypes, with regard to the three single nucleotide polymorphisms (SNPs), we found that individuals with two or three protective genotypes exhibited a significantly lower risk of recurrent miscarriage than those with no or only one protective genotype (adjusted OR = 0.369, 95% CI = 0.199–0.684, p = 0.002). Moreover, the decrease in recurrent miscarriage risk with two or three protective genotypes was most pronounced in women less than 35 years of age (OR = 0.290, 95% CI = 0.142–0.589, p < 0.001) and in women with 2–3 miscarriages (adjusted OR = 0.270, 95% CI = 0.126–0.580, p < 0.001). In conclusion, our study suggests that the rs619586 G variant may have potential protective effects conferring a decreased risk of recurrent miscarriage in the southern Chinese population.
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spelling pubmed-64659542019-04-25 The lncRNA MALAT1 rs619586 G Variant Confers Decreased Susceptibility to Recurrent Miscarriage Che, Di Yang, Yanfang Xu, Yufen Fang, Zhenzhen Pi, Lei Fu, LanYan Zhou, Huazhong Tan, Yaqian Lu, Zhaoliang Li, Li Liang, Qihua Xuan, Qingshan Gu, Xiaoqiong Front Physiol Physiology Cardiovascula disease and recurrent miscarriage have shared risk factors, and some cardiovascular disease-related candidate genes have been confirmed to be associated with recurrent miscarriage. Metastasis-associated lung adenocarcinoma transcript 1 (MALAT1) is a long non-coding RNA (lncRNA) that is considered to be associated with susceptibility to cardiovascular disease. However, whether lncRNA MALAT1 polymorphisms are related to recurrent miscarriage susceptibility is unclear. We genotyped three lncRNA MALAT1 polymorphisms (rs591291, rs619586, and rs3200401) in 284 patients and 392 controls using TaqMan methods. Logistic regression was used to evaluate the odds ratios (ORs) and 95% confidence intervals (CIs) adjusted for age. Our results showed that the rs619586 G variant had protective effects against recurrent miscarriage (AG vs. AA: adjusted OR = 0.670, 95% CI = 0.457–0.982, p = 0.040; GG vs. AA: adjusted OR = 0.278, 95% CI = 0.079–0.975, p = 0.046; GG/AG vs. AA adjusted OR = 0.621, 95% CI = 0.429–0.900, p = 0.012). In a combined analyses of protective genotypes, with regard to the three single nucleotide polymorphisms (SNPs), we found that individuals with two or three protective genotypes exhibited a significantly lower risk of recurrent miscarriage than those with no or only one protective genotype (adjusted OR = 0.369, 95% CI = 0.199–0.684, p = 0.002). Moreover, the decrease in recurrent miscarriage risk with two or three protective genotypes was most pronounced in women less than 35 years of age (OR = 0.290, 95% CI = 0.142–0.589, p < 0.001) and in women with 2–3 miscarriages (adjusted OR = 0.270, 95% CI = 0.126–0.580, p < 0.001). In conclusion, our study suggests that the rs619586 G variant may have potential protective effects conferring a decreased risk of recurrent miscarriage in the southern Chinese population. Frontiers Media S.A. 2019-04-09 /pmc/articles/PMC6465954/ /pubmed/31024342 http://dx.doi.org/10.3389/fphys.2019.00385 Text en Copyright © 2019 Che, Yang, Xu, Fang, Pi, Fu, Zhou, Tan, Lu, Li, Liang, Xuan and Gu. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Che, Di
Yang, Yanfang
Xu, Yufen
Fang, Zhenzhen
Pi, Lei
Fu, LanYan
Zhou, Huazhong
Tan, Yaqian
Lu, Zhaoliang
Li, Li
Liang, Qihua
Xuan, Qingshan
Gu, Xiaoqiong
The lncRNA MALAT1 rs619586 G Variant Confers Decreased Susceptibility to Recurrent Miscarriage
title The lncRNA MALAT1 rs619586 G Variant Confers Decreased Susceptibility to Recurrent Miscarriage
title_full The lncRNA MALAT1 rs619586 G Variant Confers Decreased Susceptibility to Recurrent Miscarriage
title_fullStr The lncRNA MALAT1 rs619586 G Variant Confers Decreased Susceptibility to Recurrent Miscarriage
title_full_unstemmed The lncRNA MALAT1 rs619586 G Variant Confers Decreased Susceptibility to Recurrent Miscarriage
title_short The lncRNA MALAT1 rs619586 G Variant Confers Decreased Susceptibility to Recurrent Miscarriage
title_sort lncrna malat1 rs619586 g variant confers decreased susceptibility to recurrent miscarriage
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6465954/
https://www.ncbi.nlm.nih.gov/pubmed/31024342
http://dx.doi.org/10.3389/fphys.2019.00385
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