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Lack of association of the alpha-ketoglutarate-dependent dioxygenase (FTO) gene polymorphisms with pulmonary tuberculosis risk: a systematic review and meta-analysis

OBJECTIVE: Our meta-analysis aims to explore the association of two single nucleotide variants; rs9939609 and rs8050136, within the FTO gene with risk of pulmonary tuberculosis (PTB). METHODS: The association of two single nucleotide variants with PTB in three genetic models was evaluated using pool...

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Autores principales: Lamichhane, Pratik, Qureshi, Maha Rahim, Islam, Nabila, Sanipini, Sailakshmn, Gopaul, Vakeanand, Razick, Shakira Dilfazeer, Agrawal, Anushka, Falfan-Valencia, Ramces
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10553135/
https://www.ncbi.nlm.nih.gov/pubmed/37811091
http://dx.doi.org/10.1097/MS9.0000000000001188
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author Lamichhane, Pratik
Qureshi, Maha Rahim
Islam, Nabila
Sanipini, Sailakshmn
Gopaul, Vakeanand
Razick, Shakira Dilfazeer
Agrawal, Anushka
Falfan-Valencia, Ramces
author_facet Lamichhane, Pratik
Qureshi, Maha Rahim
Islam, Nabila
Sanipini, Sailakshmn
Gopaul, Vakeanand
Razick, Shakira Dilfazeer
Agrawal, Anushka
Falfan-Valencia, Ramces
author_sort Lamichhane, Pratik
collection PubMed
description OBJECTIVE: Our meta-analysis aims to explore the association of two single nucleotide variants; rs9939609 and rs8050136, within the FTO gene with risk of pulmonary tuberculosis (PTB). METHODS: The association of two single nucleotide variants with PTB in three genetic models was evaluated using pooled odds ratios (ORs) with 95% CIs. RESULTS: No significant association was observed between the rs9939609 polymorphism and PTB when assuming an allelic model (OR: 1.10; 95% CI: 0.85–1.41; P=0.47; I(2) = 64.98%), a recessive model (OR: 2.04; 95% CI: 0.87–4.77; P=0.10; I(2) = 67.18%), or a dominant model (OR: 0.96; 95% CI: 0.83–1.11; P=0.56; I(2) = 27.45%). Likewise, no association was observed between rs8050136 polymorphism and PTB when assuming allelic model (OR: 1.17; 95% CI: 0.87–1.58; P=0.31; I(2) = 64.20%) or recessive model (OR: 1.04; 95% CI: 0.32–3.38; P=0.95; I(2) = 68.82%) or dominant model (OR: 1.22; 95% CI: 0.87–1.71; P=0.26; I(2) = 58.69%). CONCLUSION: There might be no association between the rs9939609 and rs8050136 variants in the FTO gene, and the risk of PTB.
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spelling pubmed-105531352023-10-06 Lack of association of the alpha-ketoglutarate-dependent dioxygenase (FTO) gene polymorphisms with pulmonary tuberculosis risk: a systematic review and meta-analysis Lamichhane, Pratik Qureshi, Maha Rahim Islam, Nabila Sanipini, Sailakshmn Gopaul, Vakeanand Razick, Shakira Dilfazeer Agrawal, Anushka Falfan-Valencia, Ramces Ann Med Surg (Lond) Reviews OBJECTIVE: Our meta-analysis aims to explore the association of two single nucleotide variants; rs9939609 and rs8050136, within the FTO gene with risk of pulmonary tuberculosis (PTB). METHODS: The association of two single nucleotide variants with PTB in three genetic models was evaluated using pooled odds ratios (ORs) with 95% CIs. RESULTS: No significant association was observed between the rs9939609 polymorphism and PTB when assuming an allelic model (OR: 1.10; 95% CI: 0.85–1.41; P=0.47; I(2) = 64.98%), a recessive model (OR: 2.04; 95% CI: 0.87–4.77; P=0.10; I(2) = 67.18%), or a dominant model (OR: 0.96; 95% CI: 0.83–1.11; P=0.56; I(2) = 27.45%). Likewise, no association was observed between rs8050136 polymorphism and PTB when assuming allelic model (OR: 1.17; 95% CI: 0.87–1.58; P=0.31; I(2) = 64.20%) or recessive model (OR: 1.04; 95% CI: 0.32–3.38; P=0.95; I(2) = 68.82%) or dominant model (OR: 1.22; 95% CI: 0.87–1.71; P=0.26; I(2) = 58.69%). CONCLUSION: There might be no association between the rs9939609 and rs8050136 variants in the FTO gene, and the risk of PTB. Lippincott Williams & Wilkins 2023-08-16 /pmc/articles/PMC10553135/ /pubmed/37811091 http://dx.doi.org/10.1097/MS9.0000000000001188 Text en Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Reviews
Lamichhane, Pratik
Qureshi, Maha Rahim
Islam, Nabila
Sanipini, Sailakshmn
Gopaul, Vakeanand
Razick, Shakira Dilfazeer
Agrawal, Anushka
Falfan-Valencia, Ramces
Lack of association of the alpha-ketoglutarate-dependent dioxygenase (FTO) gene polymorphisms with pulmonary tuberculosis risk: a systematic review and meta-analysis
title Lack of association of the alpha-ketoglutarate-dependent dioxygenase (FTO) gene polymorphisms with pulmonary tuberculosis risk: a systematic review and meta-analysis
title_full Lack of association of the alpha-ketoglutarate-dependent dioxygenase (FTO) gene polymorphisms with pulmonary tuberculosis risk: a systematic review and meta-analysis
title_fullStr Lack of association of the alpha-ketoglutarate-dependent dioxygenase (FTO) gene polymorphisms with pulmonary tuberculosis risk: a systematic review and meta-analysis
title_full_unstemmed Lack of association of the alpha-ketoglutarate-dependent dioxygenase (FTO) gene polymorphisms with pulmonary tuberculosis risk: a systematic review and meta-analysis
title_short Lack of association of the alpha-ketoglutarate-dependent dioxygenase (FTO) gene polymorphisms with pulmonary tuberculosis risk: a systematic review and meta-analysis
title_sort lack of association of the alpha-ketoglutarate-dependent dioxygenase (fto) gene polymorphisms with pulmonary tuberculosis risk: a systematic review and meta-analysis
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10553135/
https://www.ncbi.nlm.nih.gov/pubmed/37811091
http://dx.doi.org/10.1097/MS9.0000000000001188
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