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Journal of Lipid Research
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    • Research Article
      Open Access

      Whole-exome sequencing reveals damaging gene variants associated with hypoalphalipoproteinemia

      Journal of Lipid Research
      Vol. 63Issue 6100209Published online: April 20, 2022
      • Weilai Dong
      • Karen H.Y. Wong
      • Youbin Liu
      • Michal Levy-Sakin
      • Wei-Chien Hung
      • Mo Li
      • and others
      Cited in Scopus: 0
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        Low levels of high density lipoprotein-cholesterol (HDL-C) are associated with an elevated risk of arteriosclerotic coronary heart disease. Heritability of HDL-C levels is high. In this research discovery study, we used whole-exome sequencing to identify damaging gene variants that may play significant roles in determining HDL-C levels. We studied 204 individuals with a mean HDL-C level of 27.8 ± 6.4 mg/dl (range: 4–36 mg/dl). Data were analyzed by statistical gene burden testing and by filtering against candidate gene lists.
        Whole-exome sequencing reveals damaging gene variants associated with hypoalphalipoproteinemia
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