Analysis of the association of ANO3/MUC15, COL4A4, RRBP1, and KLK1 polymorphisms with COPD susceptibility in the Kashi population
Abstract Objective Chronic obstructive pulmonary disease (COPD) is a complex, multifactorial, polygenic disease. The rate of occurrence of COPD in the Kashi population (Uyghur) is significantly higher than that observed nationwide. The identification of COPD-related genes in the Chinese Uyghur popul...
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BMC
2022-05-01
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Series: | BMC Pulmonary Medicine |
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Online Access: | https://doi.org/10.1186/s12890-022-01975-3 |
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author | Lifeng Tang Xuemei Zhong Hui Gong Maimaitiaili Tuerxun Tao Ma Jie Ren Chengxin Xie Aifang Zheng Zulipikaer Abudureheman Ayiguzali Abudukadeer Paierda Aini Subinuer Yilamujiang Li Li |
author_facet | Lifeng Tang Xuemei Zhong Hui Gong Maimaitiaili Tuerxun Tao Ma Jie Ren Chengxin Xie Aifang Zheng Zulipikaer Abudureheman Ayiguzali Abudukadeer Paierda Aini Subinuer Yilamujiang Li Li |
author_sort | Lifeng Tang |
collection | DOAJ |
description | Abstract Objective Chronic obstructive pulmonary disease (COPD) is a complex, multifactorial, polygenic disease. The rate of occurrence of COPD in the Kashi population (Uyghur) is significantly higher than that observed nationwide. The identification of COPD-related genes in the Chinese Uyghur population could provide useful insights that could help us understand this phenomenon. Our previous whole-exome sequencing study of three Uyghur families with COPD demonstrated that 72 mutations in 55 genes might be associated with COPD; these included rs15783G > A in the anoctamin 3 (ANO3) gene/mucin 15 (MUC15) gene, rs1800517G > A in the collagen type IV alpha 4 chain (COL4A4) gene, rs11960G > A in the ribosome binding protein 1 (RRBP1) gene, and rs5516C > G in the kallikrein 1 (KLK1) gene. This case–control study aimed to further validate the association of the four mutations with COPD in the Chinese Uyghur population. Methods Sanger sequencing was used for the genotyping of four polymorphisms (ANO3/MUC15 rs15783, COL4A4 rs1800517, RRBP1 rs11960, and KLK1 rs5516) in 541 unrelated Uyghur COPD patients and 534 Uyghur healthy controls. We then conducted stratified analyses based on the smoking status and airflow limitation severity, to explore the correlation between selected gene polymorphisms and COPD. Results ANO3/MUC15 rs15783 and KLK1 rs5516 polymorphisms could significantly reduce COPD risk (p < 0.05), but COL4A4 rs1800517 and RRBP1 rs11960 polymorphisms were not correlated with COPD in the entire population. In a stratified analysis of smoking status, non-smokers with the ANO3/MUC15 rs15783G/G genotype (OR = 0.63, p = 0.032) or COL4A4 rs1800517 allele G (OR = 0.80, p = 0.023) had a reduced risk of COPD. Smokers with the RRBP1 rs11960A/G genotype had a lower risk of COPD (OR = 0.41, p = 0.025). The KLK1 rs5516G > C polymorphism was associated with a decreased risk of COPD (OR < 1, p < 0.05), irrespective of the smoking status of individuals. No significant association with COPD severity was observed in individuals with these four polymorphisms (p > 0.05). Conclusion We identified four previously unreported mutations (ANO3/MUC15 rs15783, COL4A4 rs1800517, RRBP1 rs11960, and KLK1 rs5516) that might decrease the COPD risk in individuals with different smoking statuses in the Chinese Uyghur population. Our findings provide new light for the genetic risk factors associated with the occurrence of COPD. |
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issn | 1471-2466 |
language | English |
last_indexed | 2024-04-13T08:19:04Z |
publishDate | 2022-05-01 |
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series | BMC Pulmonary Medicine |
spelling | doaj.art-838d0ddc37474846ad3e733494a89b312022-12-22T02:54:41ZengBMCBMC Pulmonary Medicine1471-24662022-05-0122111210.1186/s12890-022-01975-3Analysis of the association of ANO3/MUC15, COL4A4, RRBP1, and KLK1 polymorphisms with COPD susceptibility in the Kashi populationLifeng Tang0Xuemei Zhong1Hui Gong2Maimaitiaili Tuerxun3Tao Ma4Jie Ren5Chengxin Xie6Aifang Zheng7Zulipikaer Abudureheman8Ayiguzali Abudukadeer9Paierda Aini10Subinuer Yilamujiang11Li Li12Department of Respiratory and Critical Care Medicine, First People’s Hospital of KashiDepartment of Respiratory and Critical Care Medicine, First People’s Hospital of KashiClinical Research Center of Infectious Diseases (Pulmonary Tuberculosis), First People’s Hospital of KashiDepartment of Respiratory and Critical Care Medicine, First People’s Hospital of KashiDepartment of Respiratory and Critical Care Medicine, First People’s Hospital of KashiDepartment of Respiratory and Critical Care Medicine, First People’s Hospital of KashiDepartment of Respiratory and Critical Care Medicine, First People’s Hospital of KashiDepartment of Respiratory and Critical Care Medicine, First People’s Hospital of KashiClinical Research Center of Infectious Diseases (Pulmonary Tuberculosis), First People’s Hospital of KashiDepartment of Respiratory and Critical Care Medicine, First People’s Hospital of KashiDepartment of Respiratory and Critical Care Medicine, First People’s Hospital of KashiClinical Research Center of Infectious Diseases (Pulmonary Tuberculosis), First People’s Hospital of KashiDepartment of Respiratory and Critical Care Medicine, First People’s Hospital of KashiAbstract Objective Chronic obstructive pulmonary disease (COPD) is a complex, multifactorial, polygenic disease. The rate of occurrence of COPD in the Kashi population (Uyghur) is significantly higher than that observed nationwide. The identification of COPD-related genes in the Chinese Uyghur population could provide useful insights that could help us understand this phenomenon. Our previous whole-exome sequencing study of three Uyghur families with COPD demonstrated that 72 mutations in 55 genes might be associated with COPD; these included rs15783G > A in the anoctamin 3 (ANO3) gene/mucin 15 (MUC15) gene, rs1800517G > A in the collagen type IV alpha 4 chain (COL4A4) gene, rs11960G > A in the ribosome binding protein 1 (RRBP1) gene, and rs5516C > G in the kallikrein 1 (KLK1) gene. This case–control study aimed to further validate the association of the four mutations with COPD in the Chinese Uyghur population. Methods Sanger sequencing was used for the genotyping of four polymorphisms (ANO3/MUC15 rs15783, COL4A4 rs1800517, RRBP1 rs11960, and KLK1 rs5516) in 541 unrelated Uyghur COPD patients and 534 Uyghur healthy controls. We then conducted stratified analyses based on the smoking status and airflow limitation severity, to explore the correlation between selected gene polymorphisms and COPD. Results ANO3/MUC15 rs15783 and KLK1 rs5516 polymorphisms could significantly reduce COPD risk (p < 0.05), but COL4A4 rs1800517 and RRBP1 rs11960 polymorphisms were not correlated with COPD in the entire population. In a stratified analysis of smoking status, non-smokers with the ANO3/MUC15 rs15783G/G genotype (OR = 0.63, p = 0.032) or COL4A4 rs1800517 allele G (OR = 0.80, p = 0.023) had a reduced risk of COPD. Smokers with the RRBP1 rs11960A/G genotype had a lower risk of COPD (OR = 0.41, p = 0.025). The KLK1 rs5516G > C polymorphism was associated with a decreased risk of COPD (OR < 1, p < 0.05), irrespective of the smoking status of individuals. No significant association with COPD severity was observed in individuals with these four polymorphisms (p > 0.05). Conclusion We identified four previously unreported mutations (ANO3/MUC15 rs15783, COL4A4 rs1800517, RRBP1 rs11960, and KLK1 rs5516) that might decrease the COPD risk in individuals with different smoking statuses in the Chinese Uyghur population. Our findings provide new light for the genetic risk factors associated with the occurrence of COPD.https://doi.org/10.1186/s12890-022-01975-3Chronic obstructive pulmonary diseaseANO3/MUC15COL4A4KLK1RRBP1Genetic polymorphism |
spellingShingle | Lifeng Tang Xuemei Zhong Hui Gong Maimaitiaili Tuerxun Tao Ma Jie Ren Chengxin Xie Aifang Zheng Zulipikaer Abudureheman Ayiguzali Abudukadeer Paierda Aini Subinuer Yilamujiang Li Li Analysis of the association of ANO3/MUC15, COL4A4, RRBP1, and KLK1 polymorphisms with COPD susceptibility in the Kashi population BMC Pulmonary Medicine Chronic obstructive pulmonary disease ANO3/MUC15 COL4A4 KLK1 RRBP1 Genetic polymorphism |
title | Analysis of the association of ANO3/MUC15, COL4A4, RRBP1, and KLK1 polymorphisms with COPD susceptibility in the Kashi population |
title_full | Analysis of the association of ANO3/MUC15, COL4A4, RRBP1, and KLK1 polymorphisms with COPD susceptibility in the Kashi population |
title_fullStr | Analysis of the association of ANO3/MUC15, COL4A4, RRBP1, and KLK1 polymorphisms with COPD susceptibility in the Kashi population |
title_full_unstemmed | Analysis of the association of ANO3/MUC15, COL4A4, RRBP1, and KLK1 polymorphisms with COPD susceptibility in the Kashi population |
title_short | Analysis of the association of ANO3/MUC15, COL4A4, RRBP1, and KLK1 polymorphisms with COPD susceptibility in the Kashi population |
title_sort | analysis of the association of ano3 muc15 col4a4 rrbp1 and klk1 polymorphisms with copd susceptibility in the kashi population |
topic | Chronic obstructive pulmonary disease ANO3/MUC15 COL4A4 KLK1 RRBP1 Genetic polymorphism |
url | https://doi.org/10.1186/s12890-022-01975-3 |
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