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Parent-offspring association of metabolic syndrome in the Framingham Heart Study

BACKGROUND: Metabolic syndrome (MetS) is a clustering of five metabolic risk factors including abdominal obesity, elevated blood pressure, hypertriglyceridemia, low high-density lipoprotein cholesterol (HDL-C), and impaired fasting glucose. Few studies have fully reported the strength of clustering...

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Autores principales: Khan, Rumana J, Gebreab, Samson Y, Riestra, Pia, Xu, Ruihua, Davis, Sharon K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4290436/
https://www.ncbi.nlm.nih.gov/pubmed/25584075
http://dx.doi.org/10.1186/1758-5996-6-140
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author Khan, Rumana J
Gebreab, Samson Y
Riestra, Pia
Xu, Ruihua
Davis, Sharon K
author_facet Khan, Rumana J
Gebreab, Samson Y
Riestra, Pia
Xu, Ruihua
Davis, Sharon K
author_sort Khan, Rumana J
collection PubMed
description BACKGROUND: Metabolic syndrome (MetS) is a clustering of five metabolic risk factors including abdominal obesity, elevated blood pressure, hypertriglyceridemia, low high-density lipoprotein cholesterol (HDL-C), and impaired fasting glucose. Few studies have fully reported the strength of clustering of these risk factors in a parent-offspring relationship. This analysis describes the associations between parents and their adult offspring in regard to MetS. It also estimates the association between each risk factor in parents and the presence of MetS in their offspring. METHODS: We analyzed data for 1193 offspring (565 sons, and 628 daughters) from the Framingham Offspring Study who attended examinations 5, 6, and 7. Information about their parents was collected from examinations 13, 14 and 15 of the Framingham Original Cohort study. We used pedigree file to combine parental and offspring’s data. Participants were classified as having the MetS according to the Adult Treatment Panel III criteria. Analyses were conducted separately for mothers and fathers. Logistic regression was used to estimate the associations. RESULTS: After adjusting for age, education, smoking, alcohol consumption and physical activity level of offspring, no significant association was found between father’s and their offspring’s MetS. Mother’s MetS was significantly and positively associated with their daughter’s MetS (adjusted odds ratio or adj OR: 1.63; 95% confidence Interval, CI:1.02-2.61), but not with their sons’ MetS. When analyzed by individual components, maternal impaired glucose (adj OR: 2.03; 95% CI: 1.02- 9.31), abdominal obesity (adj OR: 1.56; 95% CI: 0.98- 2.55) and low HDL-C (adj OR: 2.12; 95% CI: 1.36-3.32) were associated daughter’s MetS. Maternal low HDL-C and raised total cholesterol showed marginal association with son’s MetS. For fathers, only impaired glucose (adj OR: 4.91; 95% CI: 2.07- 11.68) was associated with their daughter’s MetS. CONCLUSIONS: Using the data from Framingham Heart Study, we demonstrate differential association of MetS and its components between parents and offspring. Mother’s MetS was strongly related with daughter’s MetS, but the association was inconsistent with son’s MetS. No association was found between father’s MetS and offspring’s Mets. These results provide evidence that daughters with mother’s MetS are in higher risk than daughters or sons with father’s MetS.
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spelling pubmed-42904362015-01-13 Parent-offspring association of metabolic syndrome in the Framingham Heart Study Khan, Rumana J Gebreab, Samson Y Riestra, Pia Xu, Ruihua Davis, Sharon K Diabetol Metab Syndr Research BACKGROUND: Metabolic syndrome (MetS) is a clustering of five metabolic risk factors including abdominal obesity, elevated blood pressure, hypertriglyceridemia, low high-density lipoprotein cholesterol (HDL-C), and impaired fasting glucose. Few studies have fully reported the strength of clustering of these risk factors in a parent-offspring relationship. This analysis describes the associations between parents and their adult offspring in regard to MetS. It also estimates the association between each risk factor in parents and the presence of MetS in their offspring. METHODS: We analyzed data for 1193 offspring (565 sons, and 628 daughters) from the Framingham Offspring Study who attended examinations 5, 6, and 7. Information about their parents was collected from examinations 13, 14 and 15 of the Framingham Original Cohort study. We used pedigree file to combine parental and offspring’s data. Participants were classified as having the MetS according to the Adult Treatment Panel III criteria. Analyses were conducted separately for mothers and fathers. Logistic regression was used to estimate the associations. RESULTS: After adjusting for age, education, smoking, alcohol consumption and physical activity level of offspring, no significant association was found between father’s and their offspring’s MetS. Mother’s MetS was significantly and positively associated with their daughter’s MetS (adjusted odds ratio or adj OR: 1.63; 95% confidence Interval, CI:1.02-2.61), but not with their sons’ MetS. When analyzed by individual components, maternal impaired glucose (adj OR: 2.03; 95% CI: 1.02- 9.31), abdominal obesity (adj OR: 1.56; 95% CI: 0.98- 2.55) and low HDL-C (adj OR: 2.12; 95% CI: 1.36-3.32) were associated daughter’s MetS. Maternal low HDL-C and raised total cholesterol showed marginal association with son’s MetS. For fathers, only impaired glucose (adj OR: 4.91; 95% CI: 2.07- 11.68) was associated with their daughter’s MetS. CONCLUSIONS: Using the data from Framingham Heart Study, we demonstrate differential association of MetS and its components between parents and offspring. Mother’s MetS was strongly related with daughter’s MetS, but the association was inconsistent with son’s MetS. No association was found between father’s MetS and offspring’s Mets. These results provide evidence that daughters with mother’s MetS are in higher risk than daughters or sons with father’s MetS. BioMed Central 2014-12-15 /pmc/articles/PMC4290436/ /pubmed/25584075 http://dx.doi.org/10.1186/1758-5996-6-140 Text en © Khan et al.; licensee BioMed Central. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Khan, Rumana J
Gebreab, Samson Y
Riestra, Pia
Xu, Ruihua
Davis, Sharon K
Parent-offspring association of metabolic syndrome in the Framingham Heart Study
title Parent-offspring association of metabolic syndrome in the Framingham Heart Study
title_full Parent-offspring association of metabolic syndrome in the Framingham Heart Study
title_fullStr Parent-offspring association of metabolic syndrome in the Framingham Heart Study
title_full_unstemmed Parent-offspring association of metabolic syndrome in the Framingham Heart Study
title_short Parent-offspring association of metabolic syndrome in the Framingham Heart Study
title_sort parent-offspring association of metabolic syndrome in the framingham heart study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4290436/
https://www.ncbi.nlm.nih.gov/pubmed/25584075
http://dx.doi.org/10.1186/1758-5996-6-140
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