Association of the HtrA1 rs11200638 Polymorphism with Neovascular Age-Related Macular Degeneration in Indonesia
Introduction: The aim of this study was to investigate the association of the HtrA1 rs11200638 polymorphism with neovascular age-related macular degeneration (nAMD) in Indonesia. Methods: This case–control study included 80 patients with nAMD and 85 controls. Demographic parameters and whole blood...
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id-ugm-repo.2818142023-11-14T01:35:01Z https://repository.ugm.ac.id/281814/ Association of the HtrA1 rs11200638 Polymorphism with Neovascular Age-Related Macular Degeneration in Indonesia Supanji, Supanji Perdamaian, Ayudha Bahana Ilham Romdhoniyyah, Dewi Fathin Sasongko, Muhammad Bayu Agni, Angela Nurini Wardhana, Firman Setya Widayanti, Tri Wahyu Prayogo, Muhammad Eko Oka, Chio Kawaichi, Masashi Clinical Sciences Introduction: The aim of this study was to investigate the association of the HtrA1 rs11200638 polymorphism with neovascular age-related macular degeneration (nAMD) in Indonesia. Methods: This case–control study included 80 patients with nAMD and 85 controls. Demographic parameters and whole blood were collected from each participant. Genomic DNA was extracted and used to assess the rs11200638 genotype by PCR and restriction enzyme digestion. Associations between the HtrA1 rs11200638 polymorphism and other risk factors for susceptibility to nAMD were assessed using the logistic regression model. Results: Significant allelic associations between the HtrA1 polymorphism and nAMD were detected (odds ratio [OR] 8.67; 95% confidence interval [CI] 4.88–15.41; P \ 0.001). Genotype analysis showed a statistical difference between the nAMD group and the control group (P \ 0.001). In the multiple adjusted logistic regression model, people with the AA genotype were more likely to have nAMD although there was a wide confidence interval (OR 19.65; 95% CI 4.52–85.38; P \ 0.001). Conclusion: Our findings show that the risk of nAMD increased in the presence of risk alleles of HtrA1 rs11200638. Springer 2021-11-02 Article PeerReviewed application/pdf en https://repository.ugm.ac.id/281814/1/Supanji_KKMK.pdf Supanji, Supanji and Perdamaian, Ayudha Bahana Ilham and Romdhoniyyah, Dewi Fathin and Sasongko, Muhammad Bayu and Agni, Angela Nurini and Wardhana, Firman Setya and Widayanti, Tri Wahyu and Prayogo, Muhammad Eko and Oka, Chio and Kawaichi, Masashi (2021) Association of the HtrA1 rs11200638 Polymorphism with Neovascular Age-Related Macular Degeneration in Indonesia. Ophthalmol Ther, 2022 (11). pp. 125-133. ISSN 2193-6528 https://link.springer.com/article/10.1007/s40123-021-00402-w https://doi.org/10.1007/s40123-021-00402-w |
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Clinical Sciences Supanji, Supanji Perdamaian, Ayudha Bahana Ilham Romdhoniyyah, Dewi Fathin Sasongko, Muhammad Bayu Agni, Angela Nurini Wardhana, Firman Setya Widayanti, Tri Wahyu Prayogo, Muhammad Eko Oka, Chio Kawaichi, Masashi Association of the HtrA1 rs11200638 Polymorphism with Neovascular Age-Related Macular Degeneration in Indonesia |
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Introduction: The aim of this study was to investigate the association of the HtrA1 rs11200638 polymorphism with neovascular age-related macular degeneration (nAMD) in
Indonesia. Methods: This case–control study included 80
patients with nAMD and 85 controls. Demographic parameters and whole blood were collected from each participant. Genomic DNA was extracted and used to assess the rs11200638
genotype by PCR and restriction enzyme digestion. Associations between the HtrA1 rs11200638 polymorphism and other risk factors for susceptibility to nAMD were assessed
using the logistic regression model. Results: Significant allelic associations between the HtrA1 polymorphism and nAMD were detected (odds ratio [OR] 8.67; 95% confidence interval [CI] 4.88–15.41; P \ 0.001). Genotype analysis showed a statistical difference between the nAMD group and the control group (P \ 0.001). In the multiple adjusted logistic
regression model, people with the AA genotype were more likely to have nAMD although there was a wide confidence interval (OR 19.65; 95% CI 4.52–85.38; P \ 0.001). Conclusion: Our findings show that the risk of nAMD increased in the presence of risk alleles of HtrA1 rs11200638. |
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Article PeerReviewed |
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Supanji, Supanji Perdamaian, Ayudha Bahana Ilham Romdhoniyyah, Dewi Fathin Sasongko, Muhammad Bayu Agni, Angela Nurini Wardhana, Firman Setya Widayanti, Tri Wahyu Prayogo, Muhammad Eko Oka, Chio Kawaichi, Masashi |
author_facet |
Supanji, Supanji Perdamaian, Ayudha Bahana Ilham Romdhoniyyah, Dewi Fathin Sasongko, Muhammad Bayu Agni, Angela Nurini Wardhana, Firman Setya Widayanti, Tri Wahyu Prayogo, Muhammad Eko Oka, Chio Kawaichi, Masashi |
author_sort |
Supanji, Supanji |
title |
Association of the HtrA1 rs11200638 Polymorphism with Neovascular Age-Related Macular Degeneration in Indonesia |
title_short |
Association of the HtrA1 rs11200638 Polymorphism with Neovascular Age-Related Macular Degeneration in Indonesia |
title_full |
Association of the HtrA1 rs11200638 Polymorphism with Neovascular Age-Related Macular Degeneration in Indonesia |
title_fullStr |
Association of the HtrA1 rs11200638 Polymorphism with Neovascular Age-Related Macular Degeneration in Indonesia |
title_full_unstemmed |
Association of the HtrA1 rs11200638 Polymorphism with Neovascular Age-Related Macular Degeneration in Indonesia |
title_sort |
association of the htra1 rs11200638 polymorphism with neovascular age-related macular degeneration in indonesia |
publisher |
Springer |
publishDate |
2021 |
url |
https://repository.ugm.ac.id/281814/1/Supanji_KKMK.pdf https://repository.ugm.ac.id/281814/ https://link.springer.com/article/10.1007/s40123-021-00402-w https://doi.org/10.1007/s40123-021-00402-w |
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1783956231759593472 |