Cargando…
An evaluation of the metabolic syndrome in a large multi-ethnic study: the Family Blood Pressure Program
BACKGROUND: The Family Blood Pressure Program is an ongoing, NHLBI-sponsored, multi-center program to study the genetic determinants of high blood pressure. The goal of this particular study was to study patterns of metabolic syndrome (MetS) in four ethnic groups: African Americans, Caucasians, Hisp...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2005
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1201342/ https://www.ncbi.nlm.nih.gov/pubmed/16076393 http://dx.doi.org/10.1186/1743-7075-2-17 |
_version_ | 1782124905577316352 |
---|---|
author | Kraja, Aldi T Rao, DC Weder, Alan B Mosley, Thomas H Turner, Stephen T Hsiung, Chao Agnes Quertermous, Thomas Cooper, Richard Curb, J David Province, Michael A |
author_facet | Kraja, Aldi T Rao, DC Weder, Alan B Mosley, Thomas H Turner, Stephen T Hsiung, Chao Agnes Quertermous, Thomas Cooper, Richard Curb, J David Province, Michael A |
author_sort | Kraja, Aldi T |
collection | PubMed |
description | BACKGROUND: The Family Blood Pressure Program is an ongoing, NHLBI-sponsored, multi-center program to study the genetic determinants of high blood pressure. The goal of this particular study was to study patterns of metabolic syndrome (MetS) in four ethnic groups: African Americans, Caucasians, Hispanics, and Asians. METHODS: A major part of participants in three networks GENOA, HyperGEN and SAPPHIRe were recruited mainly through hypertensive probands. MetS was defined as a categorical trait following the National Cholesterol Education Program definition (c-MetS). MetS was also characterized quantitatively through multivariate factor analyses (FA) of 10 risk variables (q-MetS). Logistic regression and frequency tables were used for studying associations among traits. RESULTS: Using the NCEP definition, the Hispanic sample, which by design was enriched for type 2 diabetes (T2D), had a very high prevalence of MetS (73%). In contrast, its prevalence in Chinese was the lowest (17%). In African Americans and Hispanics, c-MetS was more prevalent in women than in men. Association of c-MetS with type 2 diabetes (T2D) was prominent in the Hispanics and African Americans, less pronounced in the Whites and Japanese, (although still significant), and weakest in the Chinese sample. Using FA without rotation, we found that the main factor loaded obesity (OBS) and blood pressure (BP) in African Americans; OBS and insulin (INS) in Hispanics, in Japanese, and in Whites; and OBS alone in Chinese. In Hispanics, Whites, and Japanese, BP loaded as a separate factor. Lipids in combination with INS also loaded in a separate factor. Using FA with Varimax rotation, 4 independent factors were identified: "Obesity-INS," "Blood pressure," "Lipids-INS," and "Central obesity." They explained about 60% of the variance present in the original risk variables. CONCLUSION: MetS ethnic differences were identified. Ascertaining for hypertension or T2D increased the MetS prevalence in networks compared with the one in the US general population. Obesity was the most prominent risk factor contributing to both c-MetS and q-MetS. INS contributed in two important factors (obesity and lipids). The information imbedded into c-MetS trait /q-MetS factors scores can contribute in future research of the MetS, especially its utilization in the genetic analysis. |
format | Text |
id | pubmed-1201342 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-12013422005-09-13 An evaluation of the metabolic syndrome in a large multi-ethnic study: the Family Blood Pressure Program Kraja, Aldi T Rao, DC Weder, Alan B Mosley, Thomas H Turner, Stephen T Hsiung, Chao Agnes Quertermous, Thomas Cooper, Richard Curb, J David Province, Michael A Nutr Metab (Lond) Research BACKGROUND: The Family Blood Pressure Program is an ongoing, NHLBI-sponsored, multi-center program to study the genetic determinants of high blood pressure. The goal of this particular study was to study patterns of metabolic syndrome (MetS) in four ethnic groups: African Americans, Caucasians, Hispanics, and Asians. METHODS: A major part of participants in three networks GENOA, HyperGEN and SAPPHIRe were recruited mainly through hypertensive probands. MetS was defined as a categorical trait following the National Cholesterol Education Program definition (c-MetS). MetS was also characterized quantitatively through multivariate factor analyses (FA) of 10 risk variables (q-MetS). Logistic regression and frequency tables were used for studying associations among traits. RESULTS: Using the NCEP definition, the Hispanic sample, which by design was enriched for type 2 diabetes (T2D), had a very high prevalence of MetS (73%). In contrast, its prevalence in Chinese was the lowest (17%). In African Americans and Hispanics, c-MetS was more prevalent in women than in men. Association of c-MetS with type 2 diabetes (T2D) was prominent in the Hispanics and African Americans, less pronounced in the Whites and Japanese, (although still significant), and weakest in the Chinese sample. Using FA without rotation, we found that the main factor loaded obesity (OBS) and blood pressure (BP) in African Americans; OBS and insulin (INS) in Hispanics, in Japanese, and in Whites; and OBS alone in Chinese. In Hispanics, Whites, and Japanese, BP loaded as a separate factor. Lipids in combination with INS also loaded in a separate factor. Using FA with Varimax rotation, 4 independent factors were identified: "Obesity-INS," "Blood pressure," "Lipids-INS," and "Central obesity." They explained about 60% of the variance present in the original risk variables. CONCLUSION: MetS ethnic differences were identified. Ascertaining for hypertension or T2D increased the MetS prevalence in networks compared with the one in the US general population. Obesity was the most prominent risk factor contributing to both c-MetS and q-MetS. INS contributed in two important factors (obesity and lipids). The information imbedded into c-MetS trait /q-MetS factors scores can contribute in future research of the MetS, especially its utilization in the genetic analysis. BioMed Central 2005-08-02 /pmc/articles/PMC1201342/ /pubmed/16076393 http://dx.doi.org/10.1186/1743-7075-2-17 Text en Copyright © 2005 Kraja et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Kraja, Aldi T Rao, DC Weder, Alan B Mosley, Thomas H Turner, Stephen T Hsiung, Chao Agnes Quertermous, Thomas Cooper, Richard Curb, J David Province, Michael A An evaluation of the metabolic syndrome in a large multi-ethnic study: the Family Blood Pressure Program |
title | An evaluation of the metabolic syndrome in a large multi-ethnic study: the Family Blood Pressure Program |
title_full | An evaluation of the metabolic syndrome in a large multi-ethnic study: the Family Blood Pressure Program |
title_fullStr | An evaluation of the metabolic syndrome in a large multi-ethnic study: the Family Blood Pressure Program |
title_full_unstemmed | An evaluation of the metabolic syndrome in a large multi-ethnic study: the Family Blood Pressure Program |
title_short | An evaluation of the metabolic syndrome in a large multi-ethnic study: the Family Blood Pressure Program |
title_sort | evaluation of the metabolic syndrome in a large multi-ethnic study: the family blood pressure program |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1201342/ https://www.ncbi.nlm.nih.gov/pubmed/16076393 http://dx.doi.org/10.1186/1743-7075-2-17 |
work_keys_str_mv | AT krajaaldit anevaluationofthemetabolicsyndromeinalargemultiethnicstudythefamilybloodpressureprogram AT raodc anevaluationofthemetabolicsyndromeinalargemultiethnicstudythefamilybloodpressureprogram AT wederalanb anevaluationofthemetabolicsyndromeinalargemultiethnicstudythefamilybloodpressureprogram AT mosleythomash anevaluationofthemetabolicsyndromeinalargemultiethnicstudythefamilybloodpressureprogram AT turnerstephent anevaluationofthemetabolicsyndromeinalargemultiethnicstudythefamilybloodpressureprogram AT hsiungchaoagnes anevaluationofthemetabolicsyndromeinalargemultiethnicstudythefamilybloodpressureprogram AT quertermousthomas anevaluationofthemetabolicsyndromeinalargemultiethnicstudythefamilybloodpressureprogram AT cooperrichard anevaluationofthemetabolicsyndromeinalargemultiethnicstudythefamilybloodpressureprogram AT curbjdavid anevaluationofthemetabolicsyndromeinalargemultiethnicstudythefamilybloodpressureprogram AT provincemichaela anevaluationofthemetabolicsyndromeinalargemultiethnicstudythefamilybloodpressureprogram AT krajaaldit evaluationofthemetabolicsyndromeinalargemultiethnicstudythefamilybloodpressureprogram AT raodc evaluationofthemetabolicsyndromeinalargemultiethnicstudythefamilybloodpressureprogram AT wederalanb evaluationofthemetabolicsyndromeinalargemultiethnicstudythefamilybloodpressureprogram AT mosleythomash evaluationofthemetabolicsyndromeinalargemultiethnicstudythefamilybloodpressureprogram AT turnerstephent evaluationofthemetabolicsyndromeinalargemultiethnicstudythefamilybloodpressureprogram AT hsiungchaoagnes evaluationofthemetabolicsyndromeinalargemultiethnicstudythefamilybloodpressureprogram AT quertermousthomas evaluationofthemetabolicsyndromeinalargemultiethnicstudythefamilybloodpressureprogram AT cooperrichard evaluationofthemetabolicsyndromeinalargemultiethnicstudythefamilybloodpressureprogram AT curbjdavid evaluationofthemetabolicsyndromeinalargemultiethnicstudythefamilybloodpressureprogram AT provincemichaela evaluationofthemetabolicsyndromeinalargemultiethnicstudythefamilybloodpressureprogram |