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Novel lipid biomarkers and associated gene polymorphism in young ST-segment elevation myocardial infarction
BACKGROUND: There is an increasing prevalence of coronary artery disease (CAD) in younger individuals. Lipid biomarkers such as lipoprotein-a (Lp-a), Apo A1, Apo B and Paraoxonase-1 (PON1) serve as important risk predictors for development of CAD. There is little evidence regarding the role of lipid...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9986731/ https://www.ncbi.nlm.nih.gov/pubmed/36574567 http://dx.doi.org/10.1016/j.ihj.2022.11.014 |
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author | Muheeb, Ghazi Gupta, Mohit Dayal Kunal, Shekhar Basia, Deepak MP, Girish Bansal, Ankit Yusuf, Jamal Mukhopadhyay, Saibal Tyagi, Sanjay Singh, Ritu |
author_facet | Muheeb, Ghazi Gupta, Mohit Dayal Kunal, Shekhar Basia, Deepak MP, Girish Bansal, Ankit Yusuf, Jamal Mukhopadhyay, Saibal Tyagi, Sanjay Singh, Ritu |
author_sort | Muheeb, Ghazi |
collection | PubMed |
description | BACKGROUND: There is an increasing prevalence of coronary artery disease (CAD) in younger individuals. Lipid biomarkers such as lipoprotein-a (Lp-a), Apo A1, Apo B and Paraoxonase-1 (PON1) serve as important risk predictors for development of CAD. There is little evidence regarding the role of lipid biomarkers and their genetic polymorphisms in young (<50 years) ST-segment elevation myocardial infarction (STEMI) patients. METHODS: This study included 110 young (18–50 years) STEMI patients and 110 healthy controls. Serum levels of Apo A1, Apo B, Paraoxonase-1 (PON-1) and Lipoprotein-associated phospholipase A2 (Lp-PLA2) were estimated for both patients as well as controls. Additionally, genetic polymorphisms in the Apo A1 (75G/A) and the PON1 (Q192R) genes were evaluated. RESULTS: Serum levels of apo B (101.31 ± 27.58 vs 75.31 ± 18.77 mg/dl; p < 0.0001), Lp(a) [87.56 ± 74.28 vs 25.81 ± 24.66 mg/dl, p < 0.0001] and Lp-PLA2 [5.97 ± 1.39 vs 3.49 ± 1.27 ng/mL, p < 0.0001] were significantly higher in patients as compared to controls. Serum levels of Apo A1 [44.76 ± 35.65 vs 95.97 ± 29.89; p < 0.0001] and PON1 [2.63 ± 1.5 vs 3.87 ± 1.47 ng/mL, p < 0.0001] were significantly lower in cases as compared with controls. Additionally, patients with genetic polymorphisms in the Apo A1 (75G/A) and the PON1 (Q192R) gene had an increased risk of STEMI. CONCLUSION: Lipid biomarkers such as Apo A1, Apo B and PON1 and their genetic polymorphism are associated with the susceptibility for STEMI in young individuals. |
format | Online Article Text |
id | pubmed-9986731 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-99867312023-03-07 Novel lipid biomarkers and associated gene polymorphism in young ST-segment elevation myocardial infarction Muheeb, Ghazi Gupta, Mohit Dayal Kunal, Shekhar Basia, Deepak MP, Girish Bansal, Ankit Yusuf, Jamal Mukhopadhyay, Saibal Tyagi, Sanjay Singh, Ritu Indian Heart J Research Brief BACKGROUND: There is an increasing prevalence of coronary artery disease (CAD) in younger individuals. Lipid biomarkers such as lipoprotein-a (Lp-a), Apo A1, Apo B and Paraoxonase-1 (PON1) serve as important risk predictors for development of CAD. There is little evidence regarding the role of lipid biomarkers and their genetic polymorphisms in young (<50 years) ST-segment elevation myocardial infarction (STEMI) patients. METHODS: This study included 110 young (18–50 years) STEMI patients and 110 healthy controls. Serum levels of Apo A1, Apo B, Paraoxonase-1 (PON-1) and Lipoprotein-associated phospholipase A2 (Lp-PLA2) were estimated for both patients as well as controls. Additionally, genetic polymorphisms in the Apo A1 (75G/A) and the PON1 (Q192R) genes were evaluated. RESULTS: Serum levels of apo B (101.31 ± 27.58 vs 75.31 ± 18.77 mg/dl; p < 0.0001), Lp(a) [87.56 ± 74.28 vs 25.81 ± 24.66 mg/dl, p < 0.0001] and Lp-PLA2 [5.97 ± 1.39 vs 3.49 ± 1.27 ng/mL, p < 0.0001] were significantly higher in patients as compared to controls. Serum levels of Apo A1 [44.76 ± 35.65 vs 95.97 ± 29.89; p < 0.0001] and PON1 [2.63 ± 1.5 vs 3.87 ± 1.47 ng/mL, p < 0.0001] were significantly lower in cases as compared with controls. Additionally, patients with genetic polymorphisms in the Apo A1 (75G/A) and the PON1 (Q192R) gene had an increased risk of STEMI. CONCLUSION: Lipid biomarkers such as Apo A1, Apo B and PON1 and their genetic polymorphism are associated with the susceptibility for STEMI in young individuals. Elsevier 2023 2022-11-26 /pmc/articles/PMC9986731/ /pubmed/36574567 http://dx.doi.org/10.1016/j.ihj.2022.11.014 Text en © 2022 Published by Elsevier, a division of RELX India, Pvt. Ltd on behalf of Cardiological Society of India. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Brief Muheeb, Ghazi Gupta, Mohit Dayal Kunal, Shekhar Basia, Deepak MP, Girish Bansal, Ankit Yusuf, Jamal Mukhopadhyay, Saibal Tyagi, Sanjay Singh, Ritu Novel lipid biomarkers and associated gene polymorphism in young ST-segment elevation myocardial infarction |
title | Novel lipid biomarkers and associated gene polymorphism in young ST-segment elevation myocardial infarction |
title_full | Novel lipid biomarkers and associated gene polymorphism in young ST-segment elevation myocardial infarction |
title_fullStr | Novel lipid biomarkers and associated gene polymorphism in young ST-segment elevation myocardial infarction |
title_full_unstemmed | Novel lipid biomarkers and associated gene polymorphism in young ST-segment elevation myocardial infarction |
title_short | Novel lipid biomarkers and associated gene polymorphism in young ST-segment elevation myocardial infarction |
title_sort | novel lipid biomarkers and associated gene polymorphism in young st-segment elevation myocardial infarction |
topic | Research Brief |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9986731/ https://www.ncbi.nlm.nih.gov/pubmed/36574567 http://dx.doi.org/10.1016/j.ihj.2022.11.014 |
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