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HTRA1 rs11200638 variant and AMD risk from a comprehensive analysis about 15,316 subjects

BACKGROUND: The high-temperature requirement factor A1 (HTRA1) gene located at 10q26 locus has been associated with age-related macular degenerative (AMD), with the significantly related polymorphism being (rs11200638, −625G/A), however, above association is not consistent. We investigated a compreh...

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Autores principales: Liu, Ying, Jin, Huipeng, Wei, Dong, Li, Wenxiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7229611/
https://www.ncbi.nlm.nih.gov/pubmed/32414342
http://dx.doi.org/10.1186/s12881-020-01047-5
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author Liu, Ying
Jin, Huipeng
Wei, Dong
Li, Wenxiu
author_facet Liu, Ying
Jin, Huipeng
Wei, Dong
Li, Wenxiu
author_sort Liu, Ying
collection PubMed
description BACKGROUND: The high-temperature requirement factor A1 (HTRA1) gene located at 10q26 locus has been associated with age-related macular degenerative (AMD), with the significantly related polymorphism being (rs11200638, −625G/A), however, above association is not consistent. We investigated a comprehensive analysis to evaluate the correlations between rs11200638 polymorphism and AMD susceptibility thoroughly addressing this issue. METHODS: An identification was covered from the PubMed and Wanfang databases until 27th Jan, 2020. Odds ratios (OR) with 95% confidence intervals (CI) were applied to evaluate the associations. After a thorough and meticulous search, 35 different articles (33 case-control studies with HWE, 22 case-control studies about wet/dry AMD) were retrieved. RESULTS: Individuals carrying A-allele or AA genotype may have an increased risk to be AMD disease. For example, there has a significantly increased relationship between rs11200638 polymorphism and AMD both for Asians (OR: 2.51, 95%CI: 2.22–2.83 for allelic contrast) and Caucasians [OR (95%CI) = 2.63(2.29–3.02) for allelic contrast]. Moreover, a similar trend in the source of control was detected. To classify the type of AMD, increased association was also observed in both wet (OR: 3.40, 95%CI: 2.90–3.99 for dominant model) and dry (OR: 2.08, 95%CI: 1.24–3.48 for dominant model) AMD. Finally, based on the different genotyping methods, increased relationships were identified by sequencing, TaqMan, PCR-RFLP and RT-PCR. CONCLUSIONS: Our meta-analysis demonstrated that HTRA1 rs11200638 polymorphism may be related to the AMD development, especially about individuals carrying A-allele or AA genotype, who may be as identified targets to detect and intervene in advance. Further studies using Larger sample size studies, including information about gene-environment interactions will be necessary to carry out.
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spelling pubmed-72296112020-05-27 HTRA1 rs11200638 variant and AMD risk from a comprehensive analysis about 15,316 subjects Liu, Ying Jin, Huipeng Wei, Dong Li, Wenxiu BMC Med Genet Research Article BACKGROUND: The high-temperature requirement factor A1 (HTRA1) gene located at 10q26 locus has been associated with age-related macular degenerative (AMD), with the significantly related polymorphism being (rs11200638, −625G/A), however, above association is not consistent. We investigated a comprehensive analysis to evaluate the correlations between rs11200638 polymorphism and AMD susceptibility thoroughly addressing this issue. METHODS: An identification was covered from the PubMed and Wanfang databases until 27th Jan, 2020. Odds ratios (OR) with 95% confidence intervals (CI) were applied to evaluate the associations. After a thorough and meticulous search, 35 different articles (33 case-control studies with HWE, 22 case-control studies about wet/dry AMD) were retrieved. RESULTS: Individuals carrying A-allele or AA genotype may have an increased risk to be AMD disease. For example, there has a significantly increased relationship between rs11200638 polymorphism and AMD both for Asians (OR: 2.51, 95%CI: 2.22–2.83 for allelic contrast) and Caucasians [OR (95%CI) = 2.63(2.29–3.02) for allelic contrast]. Moreover, a similar trend in the source of control was detected. To classify the type of AMD, increased association was also observed in both wet (OR: 3.40, 95%CI: 2.90–3.99 for dominant model) and dry (OR: 2.08, 95%CI: 1.24–3.48 for dominant model) AMD. Finally, based on the different genotyping methods, increased relationships were identified by sequencing, TaqMan, PCR-RFLP and RT-PCR. CONCLUSIONS: Our meta-analysis demonstrated that HTRA1 rs11200638 polymorphism may be related to the AMD development, especially about individuals carrying A-allele or AA genotype, who may be as identified targets to detect and intervene in advance. Further studies using Larger sample size studies, including information about gene-environment interactions will be necessary to carry out. BioMed Central 2020-05-15 /pmc/articles/PMC7229611/ /pubmed/32414342 http://dx.doi.org/10.1186/s12881-020-01047-5 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Liu, Ying
Jin, Huipeng
Wei, Dong
Li, Wenxiu
HTRA1 rs11200638 variant and AMD risk from a comprehensive analysis about 15,316 subjects
title HTRA1 rs11200638 variant and AMD risk from a comprehensive analysis about 15,316 subjects
title_full HTRA1 rs11200638 variant and AMD risk from a comprehensive analysis about 15,316 subjects
title_fullStr HTRA1 rs11200638 variant and AMD risk from a comprehensive analysis about 15,316 subjects
title_full_unstemmed HTRA1 rs11200638 variant and AMD risk from a comprehensive analysis about 15,316 subjects
title_short HTRA1 rs11200638 variant and AMD risk from a comprehensive analysis about 15,316 subjects
title_sort htra1 rs11200638 variant and amd risk from a comprehensive analysis about 15,316 subjects
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7229611/
https://www.ncbi.nlm.nih.gov/pubmed/32414342
http://dx.doi.org/10.1186/s12881-020-01047-5
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