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Cited by 262

The DOI matches its Crossref record; 40 of the 40 references it cites were found in a registry or an index.

Inheritance of low density lipoprotein subclass patterns in familial combined hyperlipidemia.

Open access
Austin, M A, Brunzell, J D, Fitch, W L, Krauss, R M·1990·Arteriosclerosis: An Official Journal of the American Heart Association, Inc.

Abstract

The inheritance of low density lipoprotein (LDL) subclass patterns was investigated in 234 members of seven large kindreds with familial combined hyperlipidemia (FCHL), a disorder characterized by elevated LDL cholesterol and/or triglyceride and increased coronary disease risk in families. Analysis of LDL subclasses by nondenaturing gradient gel electrophoresis showed a predominance of large, buoyant LDL particles (pattern A) in 71% of the family members and a predominance of small, dense LDL particles (pattern B) in 29% of family members. Based on complex segregation analysis, pattern B appeared to be inherited as an autosomal trait with either a dominant or an additive mode of inheritance and a small, but significant, multifactorial inheritance component. The proposed allele for pattern B was common (frequency = 0.3), and reduced penetrance was observed among men under age 20 and among women under age 50. These results in these FCHL families are consistent with those from a previously reported population-based sample of families, in which pattern B showed an apparent dominant mode of inheritance. In that study, reduced penetrance was observed for men under age 20 and for premenopausal women, but a somewhat lower allele frequency was found for pattern B (0.25). In the FCHL family members, LDL subclass pattern B was associated with significantly increased plasma levels of apolipoprotein B and triglyceride and decreased high density lipoprotein cholesterol. In comparison with a group of controls, the FCHL family members with pattern A had similar mean triglyceride levels, but higher mean apolipoprotein B. Thus, in families with FCHL, a predominance of small, dense LDL particles appears to be inherited as a common, single-gene trait, which is closely associated with the higher plasma triglyceride levels found in these families. The increased plasma apolipoprotein B levels found in FCHL cannot, however, be accounted for by this proposed locus.

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Metadata

Authors
Austin, M. A., Brunzell, J. D., Fitch, W. L., & Krauss, R. M.
Venue
Arteriosclerosis: An Official Journal of the American Heart Association, Inc.
Published
1990-07
Volume
10
Issue
4
Pages
520-530
ISSN
0276-5047 (ISSN-L)
OpenAlex
W2045872267
Cited by
262
References
40
FWCI
24.09
Type
journal article
Language
en
Open access
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CoChat. (2026). Citation check: Inheritance of low density lipoprotein subclass patterns in familial combined hyperlipidemia. https://app.cochat.ai/papers/10.1161/01.atv.10.4.520
The paper
Austin, M. A., Brunzell, J. D., Fitch, W. L., & Krauss, R. M. (1990). Inheritance of low density lipoprotein subclass patterns in familial combined hyperlipidemia. Arteriosclerosis: An Official Journal of the American Heart Association, Inc. https://doi.org/10.1161/01.atv.10.4.520

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.