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Novel Cardiovascular Risk Markers in Nigerian Cigarette Smokers

BACKGROUND: Cardiovascular disease (CVD) is the leading cause of mortality and morbidity worldwide. While the effect of cigarette smoking on conventional markers that account for <50% of CVD s has been well studied, there are only a few studies on the effect of cigarette smoking on novel cardiova...

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Autores principales: Adunmo, Godwin O, Adesokan, AbdulFatah Ayoade, Desalu, Olufemi Olumuyiwa, Biliaminu, Sikiru Abayomi, Adunmo, Eyitayo O
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5590377/
https://www.ncbi.nlm.nih.gov/pubmed/28904914
http://dx.doi.org/10.4103/ijabmr.IJABMR_140_16
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author Adunmo, Godwin O
Adesokan, AbdulFatah Ayoade
Desalu, Olufemi Olumuyiwa
Biliaminu, Sikiru Abayomi
Adunmo, Eyitayo O
author_facet Adunmo, Godwin O
Adesokan, AbdulFatah Ayoade
Desalu, Olufemi Olumuyiwa
Biliaminu, Sikiru Abayomi
Adunmo, Eyitayo O
author_sort Adunmo, Godwin O
collection PubMed
description BACKGROUND: Cardiovascular disease (CVD) is the leading cause of mortality and morbidity worldwide. While the effect of cigarette smoking on conventional markers that account for <50% of CVD s has been well studied, there are only a few studies on the effect of cigarette smoking on novel cardiovascular (CV) risk markers. OBJECTIVE: To evaluate the effect of cigarette smoking on the novel CV markers such as homocysteine (HCY), lipoprotein (a) (Lp(a)), and C-reactive protein (CRP). MATERIALS AND METHODS: One hundred and forty smokers, 12 ex-smokers, and 84 controls were recruited for the study. A structured questionnaire was used to obtain information on their clinical history, daily cigarette consumption, and duration of smoking. The smokers were further grouped according to the amount of cigarette consumption: light (<5 sticks/day), moderate (6–10 sticks/day), and heavy (>10 sticks/day) and duration of smoking: short (5–10 years), medium (11–20 years), and long (>20 years). HCY was determined by enzyme-linked immunosorbent assay method, and Lp(a) and CRP were determined spectrophotometrically. RESULTS: HCY, Lp(a), and CRP were significantly elevated in smokers when compared with control (P < 0.05) and they correlated with daily cigarette consumption and duration of smoking. Ex-smokers also exhibited a significant increase in HCY, Lp(a), and CRP level (P < 0.05) when compared with the control, but were significantly lower than the current smokers. CONCLUSION: There is a linear relationship between the intensity and duration of cigarette smoking and serum levels of all three novel risk CV markers. These findings suggest that these markers may be an important mechanism by which smoking promotes atherosclerosis.
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spelling pubmed-55903772017-09-13 Novel Cardiovascular Risk Markers in Nigerian Cigarette Smokers Adunmo, Godwin O Adesokan, AbdulFatah Ayoade Desalu, Olufemi Olumuyiwa Biliaminu, Sikiru Abayomi Adunmo, Eyitayo O Int J Appl Basic Med Res Original Article BACKGROUND: Cardiovascular disease (CVD) is the leading cause of mortality and morbidity worldwide. While the effect of cigarette smoking on conventional markers that account for <50% of CVD s has been well studied, there are only a few studies on the effect of cigarette smoking on novel cardiovascular (CV) risk markers. OBJECTIVE: To evaluate the effect of cigarette smoking on the novel CV markers such as homocysteine (HCY), lipoprotein (a) (Lp(a)), and C-reactive protein (CRP). MATERIALS AND METHODS: One hundred and forty smokers, 12 ex-smokers, and 84 controls were recruited for the study. A structured questionnaire was used to obtain information on their clinical history, daily cigarette consumption, and duration of smoking. The smokers were further grouped according to the amount of cigarette consumption: light (<5 sticks/day), moderate (6–10 sticks/day), and heavy (>10 sticks/day) and duration of smoking: short (5–10 years), medium (11–20 years), and long (>20 years). HCY was determined by enzyme-linked immunosorbent assay method, and Lp(a) and CRP were determined spectrophotometrically. RESULTS: HCY, Lp(a), and CRP were significantly elevated in smokers when compared with control (P < 0.05) and they correlated with daily cigarette consumption and duration of smoking. Ex-smokers also exhibited a significant increase in HCY, Lp(a), and CRP level (P < 0.05) when compared with the control, but were significantly lower than the current smokers. CONCLUSION: There is a linear relationship between the intensity and duration of cigarette smoking and serum levels of all three novel risk CV markers. These findings suggest that these markers may be an important mechanism by which smoking promotes atherosclerosis. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5590377/ /pubmed/28904914 http://dx.doi.org/10.4103/ijabmr.IJABMR_140_16 Text en Copyright: © 2017 International Journal of Applied and Basic Medical Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Adunmo, Godwin O
Adesokan, AbdulFatah Ayoade
Desalu, Olufemi Olumuyiwa
Biliaminu, Sikiru Abayomi
Adunmo, Eyitayo O
Novel Cardiovascular Risk Markers in Nigerian Cigarette Smokers
title Novel Cardiovascular Risk Markers in Nigerian Cigarette Smokers
title_full Novel Cardiovascular Risk Markers in Nigerian Cigarette Smokers
title_fullStr Novel Cardiovascular Risk Markers in Nigerian Cigarette Smokers
title_full_unstemmed Novel Cardiovascular Risk Markers in Nigerian Cigarette Smokers
title_short Novel Cardiovascular Risk Markers in Nigerian Cigarette Smokers
title_sort novel cardiovascular risk markers in nigerian cigarette smokers
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5590377/
https://www.ncbi.nlm.nih.gov/pubmed/28904914
http://dx.doi.org/10.4103/ijabmr.IJABMR_140_16
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