Familial Resemblance in Low-Density Lipoprotein Cholesterol Response to Statins in the Danish Population

被引:0
作者
Corn, Giulia [1 ]
Lund, Marie [1 ,2 ,3 ]
Hlatky, Mark A. [4 ,5 ]
Wohlfahrt, Jan [1 ]
Melbye, Mads [3 ,6 ,7 ,8 ]
机构
[1] Statens Serum Inst, Dept Epidemiol Res, Artillerivej 5, DK-2300 Copenhagen S, Denmark
[2] Copenhagen Univ Hosp Bispebjerg, Dept Clin Pharmacol, Copenhagen, Denmark
[3] Univ Copenhagen, Dept Clin Med, Copenhagen, Denmark
[4] Stanford Univ, Sch Med, Dept Hlth Policy, Stanford, CA 94305 USA
[5] Stanford Univ, Sch Med, Dept Med, Stanford, CA 94305 USA
[6] Stanford Univ, Sch Med, Dept Genet, Stanford, CA 94305 USA
[7] Norwegian Inst Publ Hlth, Ctr Fertil & Hlth, Oslo, Norway
[8] Norwegian Univ Sci & Technol, KG Jebsen Ctr Genet Epidemiol, Trondheim, Norway
来源
JOURNAL OF THE AMERICAN HEART ASSOCIATION | 2022年 / 11卷 / 11期
关键词
familial environment; genetic; inheritance; LDL-C; statin response; METAANALYSIS;
D O I
10.1161/JAHA.121.025465
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Change in low-density lipoprotein cholesterol (LDL-C) level after statin initiation varies widely among individuals, and in part may be because of factors shared by family members. Methods and Results We used the Danish national registers to identify 89 006 individuals who initiated statins between 2008 and 2018 and had LDL-C measured immediately before and after the start of treatment. Among these, we identified 5148 first-degree relatives and 3198 spouses. We decomposed the variation in attained LDL-C level after statin initiation by applying a mixed-effect model with 5 variance components (inter-family and inter-individual variance in pre-statin LDL-C level, inter-family and inter-individual variance in statin response, and residual variance). Results were presented as a percentage of the total variance explained by the different variance components. We found that half of the variation in attained LDL-C level after statin initiation consisted of variance in statin response, approximately one third of variance in pre-statin LDL-C level, and the remaining 10% to 15% of residual variance. While the inter-individual variance in statin response accounted for almost half of the LDL-C variation in both cohorts, the inter-family variance in statin response accounted for 3.3% among first-degree relatives and for 6.0% among spouses. Conclusions Individual factors account for most of the variation in LDL-C level after statin initiation; factors affecting statin response common within spouses and first-degree relatives account for a similar share of variation. These results suggest a modest influence of shared genetics and shared familial environment on statin response.
引用
收藏
页数:27
相关论文
共 16 条
  • [1] [Anonymous], DOCUMENTATION REGIST
  • [2] Danish registers on personal income and transfer payments
    Baadsgaard, Mikkel
    Quitzau, Jarl
    [J]. SCANDINAVIAN JOURNAL OF PUBLIC HEALTH, 2011, 39 : 103 - 105
  • [3] Efficacy and safety of more intensive lowering of LDL cholesterol: a meta-analysis of data from 170 000 participants in 26 randomised trials
    Baigent, C.
    Blackwell, L.
    Emberson, J.
    Holland, L. E.
    Reith, C.
    Bhala, N.
    Peto, R.
    Barnes, E. H.
    Keech, A.
    Simes, J.
    Collins, R.
    [J]. LANCET, 2010, 376 (9753) : 1670 - 1681
  • [4] Very Low Levels of Atherogenic Lipoproteins and the Risk for Cardiovascular Events A Meta-Analysis of Statin Trials
    Boekholdt, S. Matthijs
    Hovingh, G. Kees
    Mora, Samia
    Arsenault, Benoit J.
    Amarenco, Pierre
    Pedersen, Terje R.
    LaRosa, John C.
    Waters, David D.
    DeMicco, David A.
    Simes, R. John
    Keech, Antony C.
    Colquhoun, David
    Hitman, Graham A.
    Betteridge, John
    Clearfield, Michael B.
    Downs, John R.
    Colhoun, Helen M.
    Gotto, Antonio M., Jr.
    Ridker, Paul M.
    Grundy, Scott M.
    Kastelein, John J. P.
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2014, 64 (05) : 485 - 494
  • [5] Grundy SM, 2019, J AM COLL CARDIOL, V73, pE285, DOI 10.1016/j.jacc.2018.11.003
  • [6] A large electronic-health-record-based genome-wide study of serum lipids
    Hoffmann, Thomas J.
    Theusch, Elizabeth
    Haldar, Tanushree
    Ranatunga, Dilrini K.
    Jorgenson, Eric
    Medina, Marisa W.
    Kvale, Mark N.
    Kwok, Pui-Yan
    Schaefer, Catherine
    Krauss, Ronald M.
    Iribarren, Carlos
    Risch, Neil
    [J]. NATURE GENETICS, 2018, 50 (03) : 401 - +
  • [7] Danish education registers
    Jensen, Vibeke M.
    Rasmussen, Astrid W.
    [J]. SCANDINAVIAN JOURNAL OF PUBLIC HEALTH, 2011, 39 : 91 - 94
  • [8] Variability of low-density lipoprotein cholesterol response with different doses of atorvastatin, rosuvastatin, and simvastatin: results from VOYAGER
    Karlson, Bjorn W.
    Wiklund, Olov
    Palmer, Michael K.
    Nicholls, Stephen J.
    Lundman, Pia
    Barter, Philip J.
    [J]. EUROPEAN HEART JOURNAL-CARDIOVASCULAR PHARMACOTHERAPY, 2016, 2 (04) : 212 - 217
  • [9] Drug utilization according to reason for prescribing: a pharmacoepidemiologic method based on an indication hierarchy
    Kildemoes, Helle Wallach
    Hendriksen, Carsten
    Andersen, Morten
    [J]. PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2012, 21 (10) : 1027 - 1035
  • [10] The Danish National Prescription Registry
    Kildemoes, Helle Wallach
    Sorensen, Henrik Toft
    Hallas, Jesper
    [J]. SCANDINAVIAN JOURNAL OF PUBLIC HEALTH, 2011, 39 : 38 - 41