04426nas a2200493 4500008004100000022001400041245010800055210006900163260001600232520296700248100001603215700002403231700002403255700001903279700001603298700002203314700002603336700002103362700002103383700001503404700002003419700002303439700002203462700002003484700002103504700002803525700002203553700002003575700002703595700001603622700002003638700001903658700002003677700002703697700002603724700002103750700002103771700002103792700001703813700001903830700002603849700002103875856003603896 2024 eng d a2380-659100aFamilial Hypercholesterolemia Variant and Cardiovascular Risk in Individuals With Elevated Cholesterol.0 aFamilial Hypercholesterolemia Variant and Cardiovascular Risk in c2024 Jan 313 a

IMPORTANCE: Familial hypercholesterolemia (FH) is a genetic disorder that often results in severely high low-density lipoprotein cholesterol (LDL-C) and high risk of premature coronary heart disease (CHD). However, the impact of FH variants on CHD risk among individuals with moderately elevated LDL-C is not well quantified.

OBJECTIVE: To assess CHD risk associated with FH variants among individuals with moderately (130-189 mg/dL) and severely (≥190 mg/dL) elevated LDL-C and to quantify excess CHD deaths attributable to FH variants in US adults.

DESIGN, SETTING, AND PARTICIPANTS: A total of 21 426 individuals without preexisting CHD from 6 US cohort studies (Atherosclerosis Risk in Communities study, Coronary Artery Risk Development in Young Adults study, Cardiovascular Health Study, Framingham Heart Study Offspring cohort, Jackson Heart Study, and Multi-Ethnic Study of Atherosclerosis) were included, 63 of whom had an FH variant. Data were collected from 1971 to 2018, and the median (IQR) follow-up was 18 (13-28) years. Data were analyzed from March to May 2023.

EXPOSURES: LDL-C, cumulative past LDL-C, FH variant status.

MAIN OUTCOMES AND MEASURES: Cox proportional hazards models estimated associations between FH variants and incident CHD. The Cardiovascular Disease Policy Model projected excess CHD deaths associated with FH variants in US adults.

RESULTS: Of the 21 426 individuals without preexisting CHD (mean [SD] age 52.1 [15.5] years; 12 041 [56.2%] female), an FH variant was found in 22 individuals with moderately elevated LDL-C (0.3%) and in 33 individuals with severely elevated LDL-C (2.5%). The adjusted hazard ratios for incident CHD comparing those with and without FH variants were 2.9 (95% CI, 1.4-6.0) and 2.6 (95% CI, 1.4-4.9) among individuals with moderately and severely elevated LDL-C, respectively. The association between FH variants and CHD was slightly attenuated when further adjusting for baseline LDL-C level, whereas the association was no longer statistically significant after adjusting for cumulative past LDL-C exposure. Among US adults 20 years and older with no history of CHD and LDL-C 130 mg/dL or higher, more than 417 000 carry an FH variant and were projected to experience more than 12 000 excess CHD deaths in those with moderately elevated LDL-C and 15 000 in those with severely elevated LDL-C compared with individuals without an FH variant.

CONCLUSIONS AND RELEVANCE: In this pooled cohort study, the presence of FH variants was associated with a 2-fold higher CHD risk, even when LDL-C was only moderately elevated. The increased CHD risk appeared to be largely explained by the higher cumulative LDL-C exposure in individuals with an FH variant compared to those without. Further research is needed to assess the value of adding genetic testing to traditional phenotypic FH screening.

1 aZhang, Yiyi1 aDron, Jacqueline, S1 aBellows, Brandon, K1 aKhera, Amit, V1 aLiu, Junxiu1 aBalte, Pallavi, P1 aOelsner, Elizabeth, C1 aAmr, Sami, Samir1 aLebo, Matthew, S1 aNagy, Anna1 aPeloso, Gina, M1 aNatarajan, Pradeep1 aRotter, Jerome, I1 aWiller, Cristen1 aBoerwinkle, Eric1 aBallantyne, Christie, M1 aLutsey, Pamela, L1 aFornage, Myriam1 aLloyd-Jones, Donald, M1 aHou, Lifang1 aPsaty, Bruce, M1 aBis, Joshua, C1 aFloyd, James, S1 aVasan, Ramachandran, S1 aHeard-Costa, Nancy, L1 aCarson, April, P1 aHall, Michael, E1 aRich, Stephen, S1 aGuo, Xiuqing1 aKazi, Dhruv, S1 ade Ferranti, Sarah, D1 aMoran, Andrew, E uhttps://chs-nhlbi.org/node/9620