Heritability and genetic loci of fatty liver in familial combined hyperlipidemia

被引:56
作者
Brouwers, Martijn C. G. J. [1 ]
Cantor, Rita M.
Kono, Naoko
Yoon, Jeong Lim
van der Kallen, Carla J. H.
Bilderbeek-Beckers, Monique A. L.
van Greevenbroek, Marleen M. J.
Lusis, Aldons J.
de Bruin, Tjerk W. A.
机构
[1] Acad Hosp Maastricht, Dept Med, Maastricht, Netherlands
[2] Acad Hosp Maastricht, Cardiovasc Res Inst Maastricht, Maastricht, Netherlands
[3] Univ Calif Los Angeles, Dept Human Genet, David Geffen Sch Med, Los Angeles, CA USA
[4] Univ Calif Los Angeles, Dept Pediat, David Geffen Sch Med, Los Angeles, CA 90024 USA
[5] Univ Calif Los Angeles, Dept Med, David Geffen Sch Med, Los Angeles, CA 90024 USA
[6] VieCuri Med Ctr Noord Limburg, Dept Radiol, Venlo, Netherlands
关键词
steatosis; nonalcoholic fatty liver disease; quantitative trait locus; linkage analysis; alanine aminotransferase;
D O I
10.1194/jlr.M600312-JLR200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
VLDL overproduction, a process that is driven by an excess amount of hepatic fat, is a well-documented feature of familial combined hyperlipidemia (FCHL). The aims of this study were to investigate whether fatty liver, measured with ultrasound and as plasma alanine aminotransferase (ALT) levels, develops against a genetic background in FCHL and to identify chromosomal loci that are linked to these traits. In total, 157 FCHL family members and 20 spouses participated in this study. Radiological evidence of fatty liver was more prevalent not only in FCHL probands (40%) but also in their relatives (35%) compared with spouses (15%) (P < 0.05). Heritability calculations revealed that 20-36% of the variability in ALT levels could be attributed to genetic factors. Nonparametric quantitative trait locus (QTL) analysis revealed three significant (P < 0.001) loci with either the ultrasound or the ALT trait in the male sample: 1q42.3, 7p12-21, and 22p13-q11; none was found in the female sample or the entire group. Of these QTLs, the 7p region was consistent over time, because reanalysis with ALT levels that were determined during a visit 5 years earlier yielded similar results. This study shows that fatty liver is a heritable aspect of FCHL. Replication of particularly the 7p region is awaited.
引用
收藏
页码:2799 / 2807
页数:9
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