TY - JOUR
T1 - Genetics, lifestyle, and low-density lipoprotein cholesterol in young and apparently healthy women
AU - Balder, Jan Willem
AU - Rimbert, Antoine
AU - Zhang, Xiang
AU - Viel, Martijn
AU - Kanninga, Roan
AU - Van DIjk, Freerk
AU - Lansberg, Peter
AU - Sinke, Richard
AU - Kuivenhoven, Jan Albert
N1 - Publisher Copyright:
© 2017 American Heart Association, Inc.
PY - 2018
Y1 - 2018
N2 - Background: Atherosclerosis starts in childhood but low-density lipoprotein cholesterol (LDL-C), a causal risk factor, is mostly studied and dealt with when clinical events have occurred. Women are usually affected later in life than men and are underdiagnosed, undertreated, and understudied in cardiovascular trials and research. This study aims at a better understanding of lifestyle and genetic factors that affect LDL-C in young women. METHODS: We randomly selected for every year of age 8 women with LDL-C =1st percentile (=50 mg/dL) and 8 women with LDL-C =99th percentile (=186 mg/dL) from 28000 female participants aged between 25 to 40 years of a population-based cohort study. The resulting groups include 119 and 121 women, respectively, of an average 33 years of age. A gene-sequencing panel was used to assess established monogenic and polygenic origins of these phenotypes. Information on lifestyle was extracted from questionnaires. A healthy lifestyle score was allocated based on a recently developed algorithm. RESULTS: Of the women with LDL-C =1st percentile, 19 (15.7%) carried mutations that are causing monogenic hypocholesterolemia and 60 (49.6%) were genetically predisposed to low LDL-C on the basis of an extremely low weighted genetic risk score. In comparison with control groups, a healthier lifestyle was not associated with low LDL-C in women without genetic predispositions. Among women with LDL-C =99th percentile, 20 women (16.8%) carried mutations that cause familial hypercholesterolemia, whereas 25 (21%) were predisposed to high LDL-C on the basis of a high-weighted genetic risk score. The women in whom no genetic origin for hypercholesterolemia could be identifed were found to exhibit a signifcantly unfavorable lifestyle in comparison with controls. CONCLUSIONS: This study highlights the need for early assessment of the cardiovascular risk profle in apparently healthy young women to identify those with LDL-C =99th percentile for their age: Frst, because, in this study, 17% of the cases were molecularly diagnosed with familial hypercholesterolemia, which needs further attention; second, because our data indicate that an unfavorable lifestyle is signifcantly associated with severe hypercholesterolemia in genetically unaffected women, which may also need further attention.
AB - Background: Atherosclerosis starts in childhood but low-density lipoprotein cholesterol (LDL-C), a causal risk factor, is mostly studied and dealt with when clinical events have occurred. Women are usually affected later in life than men and are underdiagnosed, undertreated, and understudied in cardiovascular trials and research. This study aims at a better understanding of lifestyle and genetic factors that affect LDL-C in young women. METHODS: We randomly selected for every year of age 8 women with LDL-C =1st percentile (=50 mg/dL) and 8 women with LDL-C =99th percentile (=186 mg/dL) from 28000 female participants aged between 25 to 40 years of a population-based cohort study. The resulting groups include 119 and 121 women, respectively, of an average 33 years of age. A gene-sequencing panel was used to assess established monogenic and polygenic origins of these phenotypes. Information on lifestyle was extracted from questionnaires. A healthy lifestyle score was allocated based on a recently developed algorithm. RESULTS: Of the women with LDL-C =1st percentile, 19 (15.7%) carried mutations that are causing monogenic hypocholesterolemia and 60 (49.6%) were genetically predisposed to low LDL-C on the basis of an extremely low weighted genetic risk score. In comparison with control groups, a healthier lifestyle was not associated with low LDL-C in women without genetic predispositions. Among women with LDL-C =99th percentile, 20 women (16.8%) carried mutations that cause familial hypercholesterolemia, whereas 25 (21%) were predisposed to high LDL-C on the basis of a high-weighted genetic risk score. The women in whom no genetic origin for hypercholesterolemia could be identifed were found to exhibit a signifcantly unfavorable lifestyle in comparison with controls. CONCLUSIONS: This study highlights the need for early assessment of the cardiovascular risk profle in apparently healthy young women to identify those with LDL-C =99th percentile for their age: Frst, because, in this study, 17% of the cases were molecularly diagnosed with familial hypercholesterolemia, which needs further attention; second, because our data indicate that an unfavorable lifestyle is signifcantly associated with severe hypercholesterolemia in genetically unaffected women, which may also need further attention.
KW - DNA copy number variations
KW - Hypercholesterolemia
KW - Hypobetalipoproteinemias
KW - Lifestyle
KW - Lipids
KW - Lipoproteins
KW - Risk factors
UR - http://www.scopus.com/inward/record.url?scp=85047768081&partnerID=8YFLogxK
U2 - 10.1161/CIRCULATIONAHA.117.032479
DO - 10.1161/CIRCULATIONAHA.117.032479
M3 - Article
C2 - 29459468
AN - SCOPUS:85047768081
SN - 0009-7322
VL - 137
SP - 820
EP - 831
JO - Circulation
JF - Circulation
IS - 8
ER -