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Relationship between 25-hydroxyvitamin D and metabolic syndrome among Jordanian adults

Evidence of the association between 25-hydroxyvitamin D (25(OH)D) and metabolic syndrome (MeS) remains uncertain and incongruent. This study aimed to determine the association between 25(OH)D and MeS among Jordanian adults. A complex multistage sampling technique was used to select a national popula...

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Autores principales: Khader, Yousef S, Batieha, Anwar, Jaddou, Hashim, Batieha, Zahi, El-Khateeb, Mohammed, Ajlouni, Kamel
Formato: Texto
Lenguaje:English
Publicado: The Korean Nutrition Society and the Korean Society of Community Nutrition 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3085802/
https://www.ncbi.nlm.nih.gov/pubmed/21556227
http://dx.doi.org/10.4162/nrp.2011.5.2.132
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author Khader, Yousef S
Batieha, Anwar
Jaddou, Hashim
Batieha, Zahi
El-Khateeb, Mohammed
Ajlouni, Kamel
author_facet Khader, Yousef S
Batieha, Anwar
Jaddou, Hashim
Batieha, Zahi
El-Khateeb, Mohammed
Ajlouni, Kamel
author_sort Khader, Yousef S
collection PubMed
description Evidence of the association between 25-hydroxyvitamin D (25(OH)D) and metabolic syndrome (MeS) remains uncertain and incongruent. This study aimed to determine the association between 25(OH)D and MeS among Jordanian adults. A complex multistage sampling technique was used to select a national population-based household sample. The present report deals exclusively with adults aged > 18 years who had complete information on all components of MeS (n = 3,234). A structured questionnaire was used to collect all relevant information. Anthropometric, clinical, and laboratory measurements were obtained. MeS was defined according to the International Diabetes Federation (IDF) definition. Of the total, 42.0% had MeS and 31.7% had 25(OH)D < 30 ng/ml. In a stratified analysis, the prevalence of MeS did not differ significantly between subjects with low and normal 25(OH)D levels for men and women in all age groups. In the multivariate analysis, the odds of MeS were not significantly different between subjects with low and normal 25(OH)D levels (OR = 0.85, 95% CI: 0.70, 1.05, P-value = 0.133). The association between 25(OH)D and MeS remained non-significant when 25(OH)D was analyzed as a continuous variable (OR = 1.004, 95% CI; 1.000, 1.008, P = 0.057) and when analyzed based on quartiles. None of the individual components of MeS were significantly associated with 25(OH)D level. This study does not provide evidence to support the association between 25(OH)D level and MeS or its individual components. Prospective studies are necessary to better determine the roles of 25(OH)D levels in the etiology of MeS.
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spelling pubmed-30858022011-05-09 Relationship between 25-hydroxyvitamin D and metabolic syndrome among Jordanian adults Khader, Yousef S Batieha, Anwar Jaddou, Hashim Batieha, Zahi El-Khateeb, Mohammed Ajlouni, Kamel Nutr Res Pract Original Research Evidence of the association between 25-hydroxyvitamin D (25(OH)D) and metabolic syndrome (MeS) remains uncertain and incongruent. This study aimed to determine the association between 25(OH)D and MeS among Jordanian adults. A complex multistage sampling technique was used to select a national population-based household sample. The present report deals exclusively with adults aged > 18 years who had complete information on all components of MeS (n = 3,234). A structured questionnaire was used to collect all relevant information. Anthropometric, clinical, and laboratory measurements were obtained. MeS was defined according to the International Diabetes Federation (IDF) definition. Of the total, 42.0% had MeS and 31.7% had 25(OH)D < 30 ng/ml. In a stratified analysis, the prevalence of MeS did not differ significantly between subjects with low and normal 25(OH)D levels for men and women in all age groups. In the multivariate analysis, the odds of MeS were not significantly different between subjects with low and normal 25(OH)D levels (OR = 0.85, 95% CI: 0.70, 1.05, P-value = 0.133). The association between 25(OH)D and MeS remained non-significant when 25(OH)D was analyzed as a continuous variable (OR = 1.004, 95% CI; 1.000, 1.008, P = 0.057) and when analyzed based on quartiles. None of the individual components of MeS were significantly associated with 25(OH)D level. This study does not provide evidence to support the association between 25(OH)D level and MeS or its individual components. Prospective studies are necessary to better determine the roles of 25(OH)D levels in the etiology of MeS. The Korean Nutrition Society and the Korean Society of Community Nutrition 2011-04 2011-04-23 /pmc/articles/PMC3085802/ /pubmed/21556227 http://dx.doi.org/10.4162/nrp.2011.5.2.132 Text en ©2010 The Korean Nutrition Society and the Korean Society of Community Nutrition http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Khader, Yousef S
Batieha, Anwar
Jaddou, Hashim
Batieha, Zahi
El-Khateeb, Mohammed
Ajlouni, Kamel
Relationship between 25-hydroxyvitamin D and metabolic syndrome among Jordanian adults
title Relationship between 25-hydroxyvitamin D and metabolic syndrome among Jordanian adults
title_full Relationship between 25-hydroxyvitamin D and metabolic syndrome among Jordanian adults
title_fullStr Relationship between 25-hydroxyvitamin D and metabolic syndrome among Jordanian adults
title_full_unstemmed Relationship between 25-hydroxyvitamin D and metabolic syndrome among Jordanian adults
title_short Relationship between 25-hydroxyvitamin D and metabolic syndrome among Jordanian adults
title_sort relationship between 25-hydroxyvitamin d and metabolic syndrome among jordanian adults
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3085802/
https://www.ncbi.nlm.nih.gov/pubmed/21556227
http://dx.doi.org/10.4162/nrp.2011.5.2.132
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