Evidence for a major gene accounting for mild elevation in LDL cholesterol: The NHLBI Family Heart Study

Hilary Coon, M. F. Leppert, F. Kronenberg, M. A. Province, R. H. Myers, D. K. Arnett, J. H. Eckfeldt, G. Heiss, R. R. Williams, Steven Hunt

Research output: Contribution to journalArticle

16 Citations (Scopus)

Abstract

Studies of rare Mendelian disorders of low density lipoprotein cholesterol (LDL-C) metabolism have identified specific genetic mutations in the LDL receptor and apolipoprotein B. Although these rare mutations account for a small proportion of LDL-C variation, twin and adoption studies indicate that at least 50% of the overall LDL-C observed variation is genetically determined. In a heterogeneous sample of 3227 subjects from the NHLBI Family Heart Study collected from four US centres, we find evidence for a common major gene accounting for mild elevations (1.25 standard deviations) in LDL-C. The analysis favored a recessive model with a frequency of 0.52 for the gene influencing elevated LDL-C, phenotypic means of 113 mg/dl for the normal genotypes and 146 mg/dl for the abnormal genotype, and a significant polygenic heritability. This statistically-inferred major gene accounted for 24% of the variation in LDL-C, with polygenes accounting for another 28% of the variation. Using parameters for major gene transmission estimated in the segregation analysis, LDL-C showed no linkage to the LDL receptor gene (LDLR), nor to the apolipoprotein E gene (APOE), nor to the cholesterol 7α-hydroxylase gene (CYP7A1), indicating the major gene effect influencing mild elevation in LDL-C is not explained by any of these candidate loci.

Original languageEnglish
Pages (from-to)401-412
Number of pages12
JournalAnnals of Human Genetics
Volume63
Issue number5
DOIs
Publication statusPublished - Sep 1999
Externally publishedYes

Fingerprint

National Heart, Lung, and Blood Institute (U.S.)
LDL Cholesterol
Genes
LDL Receptors
Genotype
Cholesterol 7-alpha-Hydroxylase
Mutation
Twin Studies
Apolipoproteins B
Apolipoproteins E
Gene Frequency

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics

Cite this

Evidence for a major gene accounting for mild elevation in LDL cholesterol : The NHLBI Family Heart Study. / Coon, Hilary; Leppert, M. F.; Kronenberg, F.; Province, M. A.; Myers, R. H.; Arnett, D. K.; Eckfeldt, J. H.; Heiss, G.; Williams, R. R.; Hunt, Steven.

In: Annals of Human Genetics, Vol. 63, No. 5, 09.1999, p. 401-412.

Research output: Contribution to journalArticle

Coon, H, Leppert, MF, Kronenberg, F, Province, MA, Myers, RH, Arnett, DK, Eckfeldt, JH, Heiss, G, Williams, RR & Hunt, S 1999, 'Evidence for a major gene accounting for mild elevation in LDL cholesterol: The NHLBI Family Heart Study', Annals of Human Genetics, vol. 63, no. 5, pp. 401-412. https://doi.org/10.1017/S000348009900771X
Coon, Hilary ; Leppert, M. F. ; Kronenberg, F. ; Province, M. A. ; Myers, R. H. ; Arnett, D. K. ; Eckfeldt, J. H. ; Heiss, G. ; Williams, R. R. ; Hunt, Steven. / Evidence for a major gene accounting for mild elevation in LDL cholesterol : The NHLBI Family Heart Study. In: Annals of Human Genetics. 1999 ; Vol. 63, No. 5. pp. 401-412.
@article{f74ff2598da545b7a1b6a1f68881add3,
title = "Evidence for a major gene accounting for mild elevation in LDL cholesterol: The NHLBI Family Heart Study",
abstract = "Studies of rare Mendelian disorders of low density lipoprotein cholesterol (LDL-C) metabolism have identified specific genetic mutations in the LDL receptor and apolipoprotein B. Although these rare mutations account for a small proportion of LDL-C variation, twin and adoption studies indicate that at least 50{\%} of the overall LDL-C observed variation is genetically determined. In a heterogeneous sample of 3227 subjects from the NHLBI Family Heart Study collected from four US centres, we find evidence for a common major gene accounting for mild elevations (1.25 standard deviations) in LDL-C. The analysis favored a recessive model with a frequency of 0.52 for the gene influencing elevated LDL-C, phenotypic means of 113 mg/dl for the normal genotypes and 146 mg/dl for the abnormal genotype, and a significant polygenic heritability. This statistically-inferred major gene accounted for 24{\%} of the variation in LDL-C, with polygenes accounting for another 28{\%} of the variation. Using parameters for major gene transmission estimated in the segregation analysis, LDL-C showed no linkage to the LDL receptor gene (LDLR), nor to the apolipoprotein E gene (APOE), nor to the cholesterol 7α-hydroxylase gene (CYP7A1), indicating the major gene effect influencing mild elevation in LDL-C is not explained by any of these candidate loci.",
author = "Hilary Coon and Leppert, {M. F.} and F. Kronenberg and Province, {M. A.} and Myers, {R. H.} and Arnett, {D. K.} and Eckfeldt, {J. H.} and G. Heiss and Williams, {R. R.} and Steven Hunt",
year = "1999",
month = "9",
doi = "10.1017/S000348009900771X",
language = "English",
volume = "63",
pages = "401--412",
journal = "Annals of Human Genetics",
issn = "0003-4800",
publisher = "Wiley-Blackwell",
number = "5",

}

TY - JOUR

T1 - Evidence for a major gene accounting for mild elevation in LDL cholesterol

T2 - The NHLBI Family Heart Study

AU - Coon, Hilary

AU - Leppert, M. F.

AU - Kronenberg, F.

AU - Province, M. A.

AU - Myers, R. H.

AU - Arnett, D. K.

AU - Eckfeldt, J. H.

AU - Heiss, G.

AU - Williams, R. R.

AU - Hunt, Steven

PY - 1999/9

Y1 - 1999/9

N2 - Studies of rare Mendelian disorders of low density lipoprotein cholesterol (LDL-C) metabolism have identified specific genetic mutations in the LDL receptor and apolipoprotein B. Although these rare mutations account for a small proportion of LDL-C variation, twin and adoption studies indicate that at least 50% of the overall LDL-C observed variation is genetically determined. In a heterogeneous sample of 3227 subjects from the NHLBI Family Heart Study collected from four US centres, we find evidence for a common major gene accounting for mild elevations (1.25 standard deviations) in LDL-C. The analysis favored a recessive model with a frequency of 0.52 for the gene influencing elevated LDL-C, phenotypic means of 113 mg/dl for the normal genotypes and 146 mg/dl for the abnormal genotype, and a significant polygenic heritability. This statistically-inferred major gene accounted for 24% of the variation in LDL-C, with polygenes accounting for another 28% of the variation. Using parameters for major gene transmission estimated in the segregation analysis, LDL-C showed no linkage to the LDL receptor gene (LDLR), nor to the apolipoprotein E gene (APOE), nor to the cholesterol 7α-hydroxylase gene (CYP7A1), indicating the major gene effect influencing mild elevation in LDL-C is not explained by any of these candidate loci.

AB - Studies of rare Mendelian disorders of low density lipoprotein cholesterol (LDL-C) metabolism have identified specific genetic mutations in the LDL receptor and apolipoprotein B. Although these rare mutations account for a small proportion of LDL-C variation, twin and adoption studies indicate that at least 50% of the overall LDL-C observed variation is genetically determined. In a heterogeneous sample of 3227 subjects from the NHLBI Family Heart Study collected from four US centres, we find evidence for a common major gene accounting for mild elevations (1.25 standard deviations) in LDL-C. The analysis favored a recessive model with a frequency of 0.52 for the gene influencing elevated LDL-C, phenotypic means of 113 mg/dl for the normal genotypes and 146 mg/dl for the abnormal genotype, and a significant polygenic heritability. This statistically-inferred major gene accounted for 24% of the variation in LDL-C, with polygenes accounting for another 28% of the variation. Using parameters for major gene transmission estimated in the segregation analysis, LDL-C showed no linkage to the LDL receptor gene (LDLR), nor to the apolipoprotein E gene (APOE), nor to the cholesterol 7α-hydroxylase gene (CYP7A1), indicating the major gene effect influencing mild elevation in LDL-C is not explained by any of these candidate loci.

UR - http://www.scopus.com/inward/record.url?scp=0033494813&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0033494813&partnerID=8YFLogxK

U2 - 10.1017/S000348009900771X

DO - 10.1017/S000348009900771X

M3 - Article

C2 - 10735582

AN - SCOPUS:0033494813

VL - 63

SP - 401

EP - 412

JO - Annals of Human Genetics

JF - Annals of Human Genetics

SN - 0003-4800

IS - 5

ER -