Heritability of features of the insulin resistance syndrome in a community-based study of healthy families
Abstract
Aims To investigate genetic and environmental influences on anthropometric, metabolic and fibrinolytic traits of the insulin resistance syndrome (IRS) in a population not characterized by a high degree of insulin resistance. Methods We recruited 537 adults from 89 randomly ascertained healthy families of white north European origin from the general population. We used maximum likelihood analysis to estimate the heritabilities and effects of environmental covariates on traits of the IRS in these families. Results Adjusted for age, sex and body mass index, the traits showed considerable heritability. For waist-hip ratio, heritability was 15%. The heritabilities of fasting glucose, insulin and estimated insulin resistance were 20%, 23% and 23%, respectively. Heritabilities were 20%, 24% and 43% for triglycerides, LDL-cholesterol and HDL-cholesterol, respectively. For PAI-1 Ag and t-PA Ag they were 20% and 26%. Covariates explained 20-25% of the variance of lipids and insulin resistance and 35-36% of fibrinolytic factors. Childhood household influences significantly affected variance for waist-hip ratio (4%), fasting insulin (11%) and estimated insulin resistance (12%). Conclusions These family data demonstrate significant genetic influence on anthropometric, fibrinolytic and glucose-related traits of the IRS in a healthy white North European population.
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Genetic factors contribute to 47.3% of variation in plasma APP activity in the Leeds Family Study, a healthy population.
“we have shown in a well established and large family study representative of a healthy population, the Leeds Family Study [Freeman et al., 2002a[Freeman et al., , 2002b]], that genetic factors contribute to 47.3% of variation in plasma APP activity.”
From A functional XPNPEP2 promoter haplotype leads to reduced plasma aminopeptidase P and increased risk of ACE inhibitor‐induced angioedema (2011) · cites this paper as Freeman et al., 2002b
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References 36 · Cited by 101
- Authors
- Freeman, M. S., Mansfield, M. W., Barrett, J. H., & Grant, P. J.
- Affiliations
- Leeds General Infirmary (GB)
- University of Leeds (GB)
- Corresponding author
- Freeman, M. S.
- Venue
- Diabetic Medicine
- Publisher
- Wiley
- Published
- 2002-12
- Volume
- 19
- Issue
- 12
- Pages
- 994-999
- ISSN
- 0742-3071 (ISSN-L)
- 1464-5491
- OpenAlex
- W2016370483
- Cited by
- 101
- References
- 36
- Citations by year
- 2024: 1 · 2021: 4 · 2020: 2 · 2019: 1 · 2017: 2 · 2016: 1 · 2015: 3 · 2014: 2 · 2013: 3 · 2012: 4
- FWCI
- 3.23
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Diabetic Medicine (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes, Cardiovascular Risks, and Lipoproteins
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Physical Performance
- Keywords
- metabolic syndrome, heritability, genetic factors, environmental variables, family studies, waist-to-hip ratio, fasting blood glucose, fasting insulin, triglycerides, lipoproteins, fibrinolytic factors, plasminogen activator inhibitor-1, tissue plasminogen activator, anthropometric traits, metabolic phenotypes
- MeSH terms
- Adolescent, Adult, Body Constitution, Child, Female, Humans, Insulin Resistance, Cholesterol, LDL, Male, Middle Aged, Triglycerides, Plasminogen Activator Inhibitor 1, Genetic Predisposition to Disease
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