Literature DB >> 21570269

Partial normalization of components of metabolic syndrome does not influence prevalent echocardiographic abnormalities: the HyperGEN study.

G de Simone1, D K Arnett, M Chinali, M De Marco, D C Rao, A T Kraja, S C Hunt, R B Devereux.   

Abstract

BACKGROUND AND AIMS: Metabolic syndrome (MetS) is a complex condition characterized by different phenotypes, according to the combinations of risk factors and is associated with cardiovascular abnormalities. Whether control of MetS components by treatment produces improvement in the associated cardiovascular abnormalities is unknown. We investigated whether partial control of components of MetS was associated with less echocardiographic abnormalities than the complete presentation of MetS based on measured components. METHODS AND
RESULTS: We evaluated markers of echocardiographic preclinical cardiovascular disease in MetS (ATP III) defined by measured components or by history of treatment, in 1421 African-American and 1195 Caucasian non-diabetic HyperGEN participants, without prevalent cardiovascular disease or serum creatinine >2 mg/dL. Of 2616 subjects, 512 subjects had MetS by measured components and 328 by history. Hypertension was found in 16% of participants without MetS, 6% of those with MetS by history and 42% of those with MetS by measured components. Obesity and central fat distribution had similar prevalence in both MetS groups (both p < 0.0001 vs. No-MetS). Blood pressure was similar in MetS by history and No-MetS, and lower than in MetS by measured components (p < 0.0001). LV mass and midwall shortening, left atrial (LA) dimension and LA systolic force were similarly abnormal in both MetS groups (all p < 0.0001 vs. No-MetS) without difference between them.
CONCLUSIONS: There is a little impact of control by treatment of single components of MetS (namely hypertension) on echocardiographic abnormalities. Lower blood pressure in participants with MetS by history was not associated with substantially reduced alterations in cardiac geometry and function.
Copyright © 2011 Elsevier B.V. All rights reserved.

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Year:  2011        PMID: 21570269      PMCID: PMC3158296          DOI: 10.1016/j.numecd.2011.02.004

Source DB:  PubMed          Journal:  Nutr Metab Cardiovasc Dis        ISSN: 0939-4753            Impact factor:   4.222


  42 in total

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3.  Association of left ventricular hypertrophy with metabolic risk factors: the HyperGEN study.

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Journal:  Hypertension       Date:  2001-09       Impact factor: 10.190

7.  NHLBI family blood pressure program: methodology and recruitment in the HyperGEN network. Hypertension genetic epidemiology network.

Authors:  R R Williams; D C Rao; R C Ellison; D K Arnett; G Heiss; A Oberman; J H Eckfeldt; M F Leppert; M A Province; S C Mockrin; S C Hunt
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9.  10-year follow-up of diabetes incidence and weight loss in the Diabetes Prevention Program Outcomes Study.

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10.  Comparison of cardiac structure and function in American Indians with and without the metabolic syndrome (the Strong Heart Study).

Authors:  Marcello Chinali; Richard B Devereux; Barbara V Howard; Mary J Roman; Jonathan N Bella; Jennifer E Liu; Helaine E Resnick; Elisa T Lee; Lyle G Best; Giovanni de Simone
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  3 in total

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Journal:  J Hypertens Manag       Date:  2017-07-20

2.  Target organ damage and incident type 2 diabetes mellitus: the Strong Heart Study.

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Review 3.  Obesity and hypertensive heart disease: focus on body composition and sex differences.

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Journal:  Diabetol Metab Syndr       Date:  2016-11-30       Impact factor: 3.320

  3 in total

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