Association of interleukin 1 receptor antagonist (IL1RN) gene polymorphism with recurrent pregnancy loss risk in the North Indian Population and a meta-analysis
| العنوان: | Association of interleukin 1 receptor antagonist (IL1RN) gene polymorphism with recurrent pregnancy loss risk in the North Indian Population and a meta-analysis |
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| المؤلفون: | Rohini R. Nair, Kiran Singh, Anuradha Khanna |
| المصدر: | Molecular Biology Reports. 41:5719-5727 |
| بيانات النشر: | Springer Science and Business Media LLC, 2014. |
| سنة النشر: | 2014 |
| مصطلحات موضوعية: | Adult, Oncology, medicine.medical_specialty, Genotype, Interleukin-1beta, Population, India, Minisatellite Repeats, Biology, Bioinformatics, White People, Young Adult, Pregnancy, Risk Factors, Polymorphism (computer science), Internal medicine, Genetics, medicine, Humans, Genetic Predisposition to Disease, Allele, education, Molecular Biology, Alleles, Genetic association, education.field_of_study, Polymorphism, Genetic, Case-control study, General Medicine, Abortion, Spontaneous, Interleukin 1 Receptor Antagonist Protein, Interleukin 1 receptor antagonist, Case-Control Studies, Population study, Female |
| الوصف: | An appropriate ratio of interleukin 1 beta to interleukin 1 receptor antagonist (IL1Ra) is required for successful pregnancy. Our objective was to study the genetic association between IL1RN variable numbers of tandem repeat (VNTR) polymorphism and recurrent pregnancy loss (RPL). To analyze the association between IL1RN VNTR allele and RPL, we investigated the IL1RN VNTR polymorphism in 136 RPL patients and in 200 healthy control women. Meta-analysis on this polymorphism was conducted to support our findings. PCR based approach was used to analyze IL1RN VNTR polymorphism and it was further confirmed by sequencing. Systematic review and meta-analysis was done using electronic database (Pub-Med, Google Scholar and Ovid) up to February 27, 2013. This meta-analysis was assessed by comprehensive meta-analysis software version 2. For meta-analysis 549 cases and 1,450 controls were included. The frequency of IL1RN genotype 2/2 was significantly higher in RPL compared to control group (AORs 3.10, 95 % CI 1.58-6.11, p = 0.001). The presence of rare allele also increased the risk of RPL significantly (ORs 1.63, 95 % CI 1.16-2.29, p = 0.004). The meta-analysis stratified by ethnicity showed that individuals with allele 2 had increased risk of RPL (OR 1.29, 95 % CI 1.04-1.61, p = 0.01), in Asians population by using fixed model. However the data of the present study clearly suggests that IL1RN VNTR polymorphism is a genetic risk factor for pregnancy loss in the study population. |
| تدمد: | 1573-4978 0301-4851 |
| الوصول الحر: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3369cdf57d2653107b0dc774899cacdTest https://doi.org/10.1007/s11033-014-3443-8Test |
| حقوق: | CLOSED |
| رقم الانضمام: | edsair.doi.dedup.....c3369cdf57d2653107b0dc774899cacd |
| قاعدة البيانات: | OpenAIRE |
| تدمد: | 15734978 03014851 |
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