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Association of metabolic syndrome and level of hs-CRP, Lp(a), and serum ferritin in young Asian patients (≤45 years) with acute myocardial infarction
AIMS: This study was aimed to determine the levels of hs-CRP, serum ferritin, and Lp(a) and to study the prevalence of metabolic syndrome (MetS) in young patients (≤45 years) with and without acute myocardial infarction (AMI). METHODS: This was a cross-sectional, case–control study conducted at a te...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Akadémiai Kiadó
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6167620/ https://www.ncbi.nlm.nih.gov/pubmed/30363361 http://dx.doi.org/10.1556/1646.10.2018.14 |
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author | Ramesh, Gadepalli Sai, Nyayapathi Venkata Balakrishna Gururaj, Pramod Bhupal, Reddy Patel, Nilesh |
author_facet | Ramesh, Gadepalli Sai, Nyayapathi Venkata Balakrishna Gururaj, Pramod Bhupal, Reddy Patel, Nilesh |
author_sort | Ramesh, Gadepalli |
collection | PubMed |
description | AIMS: This study was aimed to determine the levels of hs-CRP, serum ferritin, and Lp(a) and to study the prevalence of metabolic syndrome (MetS) in young patients (≤45 years) with and without acute myocardial infarction (AMI). METHODS: This was a cross-sectional, case–control study conducted at a tertiary care center in India. Equal number of patients with matched age and sex (n = 51) were included in case group (with AMI) and in control group (without AMI). Subjects were assessed for the presence of MetS as per modified ATP III criteria. The hs-CRP, Lp(a), and serum ferritin were also measured. RESULTS: The prevalence of MetS was found to be 62.74% in case group, whereas 33.33% in control group with decreased HDL level as the most prevalent parameter. The hs-CRP level was found to be 15.35 ± 8.27 mg/dl in case group and 1.85 ± 1.05 mg/dl in control group and Lp(a) was 33.84 ± 23.69 mg/dl in case group and 19.68 ± 10.39 mg/dl in control group. No significant difference was observed in the serum ferritin level in case (264.2 ± 40.6 ng/dl) and control (225.51 ± 45.35 ng/dl) groups. CONCLUSION: From this study, we can conclude that the assessment of these novel risk factors [hs-CRP, Lp(a), and MetS] may be used for the risk estimation and can help to prevent future mortality and morbidity due to CVD. |
format | Online Article Text |
id | pubmed-6167620 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Akadémiai Kiadó |
record_format | MEDLINE/PubMed |
spelling | pubmed-61676202018-10-24 Association of metabolic syndrome and level of hs-CRP, Lp(a), and serum ferritin in young Asian patients (≤45 years) with acute myocardial infarction Ramesh, Gadepalli Sai, Nyayapathi Venkata Balakrishna Gururaj, Pramod Bhupal, Reddy Patel, Nilesh Interv Med Appl Sci Original Paper AIMS: This study was aimed to determine the levels of hs-CRP, serum ferritin, and Lp(a) and to study the prevalence of metabolic syndrome (MetS) in young patients (≤45 years) with and without acute myocardial infarction (AMI). METHODS: This was a cross-sectional, case–control study conducted at a tertiary care center in India. Equal number of patients with matched age and sex (n = 51) were included in case group (with AMI) and in control group (without AMI). Subjects were assessed for the presence of MetS as per modified ATP III criteria. The hs-CRP, Lp(a), and serum ferritin were also measured. RESULTS: The prevalence of MetS was found to be 62.74% in case group, whereas 33.33% in control group with decreased HDL level as the most prevalent parameter. The hs-CRP level was found to be 15.35 ± 8.27 mg/dl in case group and 1.85 ± 1.05 mg/dl in control group and Lp(a) was 33.84 ± 23.69 mg/dl in case group and 19.68 ± 10.39 mg/dl in control group. No significant difference was observed in the serum ferritin level in case (264.2 ± 40.6 ng/dl) and control (225.51 ± 45.35 ng/dl) groups. CONCLUSION: From this study, we can conclude that the assessment of these novel risk factors [hs-CRP, Lp(a), and MetS] may be used for the risk estimation and can help to prevent future mortality and morbidity due to CVD. Akadémiai Kiadó 2018-04-13 2018-06 /pmc/articles/PMC6167620/ /pubmed/30363361 http://dx.doi.org/10.1556/1646.10.2018.14 Text en © 2018 The Author(s) http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium for non-commercial purposes, provided the original author and source are credited, a link to the CC License is provided, and changes – if any – are indicated. |
spellingShingle | Original Paper Ramesh, Gadepalli Sai, Nyayapathi Venkata Balakrishna Gururaj, Pramod Bhupal, Reddy Patel, Nilesh Association of metabolic syndrome and level of hs-CRP, Lp(a), and serum ferritin in young Asian patients (≤45 years) with acute myocardial infarction |
title | Association of metabolic syndrome and level of hs-CRP, Lp(a), and serum ferritin in young Asian patients (≤45 years) with acute myocardial infarction |
title_full | Association of metabolic syndrome and level of hs-CRP, Lp(a), and serum ferritin in young Asian patients (≤45 years) with acute myocardial infarction |
title_fullStr | Association of metabolic syndrome and level of hs-CRP, Lp(a), and serum ferritin in young Asian patients (≤45 years) with acute myocardial infarction |
title_full_unstemmed | Association of metabolic syndrome and level of hs-CRP, Lp(a), and serum ferritin in young Asian patients (≤45 years) with acute myocardial infarction |
title_short | Association of metabolic syndrome and level of hs-CRP, Lp(a), and serum ferritin in young Asian patients (≤45 years) with acute myocardial infarction |
title_sort | association of metabolic syndrome and level of hs-crp, lp(a), and serum ferritin in young asian patients (≤45 years) with acute myocardial infarction |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6167620/ https://www.ncbi.nlm.nih.gov/pubmed/30363361 http://dx.doi.org/10.1556/1646.10.2018.14 |
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