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Distribution of APOE gene polymorphism in the Chinese Uyghur children & its association with urolithiasis
BACKGROUND & OBJECTIVES: This study was to survey the apolipoprotein E (APOE) gene polymorphism distribution among Chinese Uyghur children and to explore the relationship between APOE gene polymorphism and the occurrence of urolithiasis. METHODS: A total of 144 Uyghur children with urolithiasis...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8715683/ https://www.ncbi.nlm.nih.gov/pubmed/34782536 http://dx.doi.org/10.4103/ijmr.IJMR_1208_18 |
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author | Huang, Yuanni Bao, Mian Liu, Caixia Zheng, Shukai Du, Taifeng Wu, Kusheng |
author_facet | Huang, Yuanni Bao, Mian Liu, Caixia Zheng, Shukai Du, Taifeng Wu, Kusheng |
author_sort | Huang, Yuanni |
collection | PubMed |
description | BACKGROUND & OBJECTIVES: This study was to survey the apolipoprotein E (APOE) gene polymorphism distribution among Chinese Uyghur children and to explore the relationship between APOE gene polymorphism and the occurrence of urolithiasis. METHODS: A total of 144 Uyghur children with urolithiasis and 274 without the history of urolithiasis were enrolled in this study. Venous blood samples were collected from all participants, and APOE genotyping, derived from rs429358 and rs7412, was performed using Sanger sequencing. RESULTS: Among the 418 children, the most prevalent genotype was E3/3, accounting for 71.3 per cent in the urolithiasis group and 71.4 per cent in the control group, followed by E3/4 and E2/3. Higher frequencies of the ɛ2 and ɛ4 alleles and lower frequencies of the ɛ3 allele were observed in the test group, and the unusual allele ɛ1 was also found in them. However, there were no significant differences between cases and controls at both rs429358 and rs7412 genotype and allele frequencies [odds ratio (OR)=0.98, 95% confidence interval (CI): 0.57-1.67; 0.98 (0.59-1.63); 1.43 (0.75-2.74) and 1.40 (0.74-2.62), respectively]. Likewise, none of significant differences was found between cases and controls at both APOE genotype and allele frequencies [OR=0.88, 95% CI: 0.51-1.53; 0.74 (0.33-1.64); 1.10 (0.73-1.66); 1.13 (0.76-1.67) and 1.14 (0.76-1.70), respectively]. INTERPRETATION & CONCLUSIONS: The present study does not support any association between APOE genotyping and urolithiasis in Uyghur children. |
format | Online Article Text |
id | pubmed-8715683 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-87156832022-01-14 Distribution of APOE gene polymorphism in the Chinese Uyghur children & its association with urolithiasis Huang, Yuanni Bao, Mian Liu, Caixia Zheng, Shukai Du, Taifeng Wu, Kusheng Indian J Med Res Original Article BACKGROUND & OBJECTIVES: This study was to survey the apolipoprotein E (APOE) gene polymorphism distribution among Chinese Uyghur children and to explore the relationship between APOE gene polymorphism and the occurrence of urolithiasis. METHODS: A total of 144 Uyghur children with urolithiasis and 274 without the history of urolithiasis were enrolled in this study. Venous blood samples were collected from all participants, and APOE genotyping, derived from rs429358 and rs7412, was performed using Sanger sequencing. RESULTS: Among the 418 children, the most prevalent genotype was E3/3, accounting for 71.3 per cent in the urolithiasis group and 71.4 per cent in the control group, followed by E3/4 and E2/3. Higher frequencies of the ɛ2 and ɛ4 alleles and lower frequencies of the ɛ3 allele were observed in the test group, and the unusual allele ɛ1 was also found in them. However, there were no significant differences between cases and controls at both rs429358 and rs7412 genotype and allele frequencies [odds ratio (OR)=0.98, 95% confidence interval (CI): 0.57-1.67; 0.98 (0.59-1.63); 1.43 (0.75-2.74) and 1.40 (0.74-2.62), respectively]. Likewise, none of significant differences was found between cases and controls at both APOE genotype and allele frequencies [OR=0.88, 95% CI: 0.51-1.53; 0.74 (0.33-1.64); 1.10 (0.73-1.66); 1.13 (0.76-1.67) and 1.14 (0.76-1.70), respectively]. INTERPRETATION & CONCLUSIONS: The present study does not support any association between APOE genotyping and urolithiasis in Uyghur children. Wolters Kluwer - Medknow 2021-07 /pmc/articles/PMC8715683/ /pubmed/34782536 http://dx.doi.org/10.4103/ijmr.IJMR_1208_18 Text en Copyright: © 2021 Indian Journal of Medical Research https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Huang, Yuanni Bao, Mian Liu, Caixia Zheng, Shukai Du, Taifeng Wu, Kusheng Distribution of APOE gene polymorphism in the Chinese Uyghur children & its association with urolithiasis |
title | Distribution of APOE gene polymorphism in the Chinese Uyghur children & its association with urolithiasis |
title_full | Distribution of APOE gene polymorphism in the Chinese Uyghur children & its association with urolithiasis |
title_fullStr | Distribution of APOE gene polymorphism in the Chinese Uyghur children & its association with urolithiasis |
title_full_unstemmed | Distribution of APOE gene polymorphism in the Chinese Uyghur children & its association with urolithiasis |
title_short | Distribution of APOE gene polymorphism in the Chinese Uyghur children & its association with urolithiasis |
title_sort | distribution of apoe gene polymorphism in the chinese uyghur children & its association with urolithiasis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8715683/ https://www.ncbi.nlm.nih.gov/pubmed/34782536 http://dx.doi.org/10.4103/ijmr.IJMR_1208_18 |
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