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Comment
. 2023 Jan;29(1):43-44.
doi: 10.1038/s41591-022-02124-3.

Genetic prediction of medication use patterns in cardiometabolic disease

No authors listed
Comment

Genetic prediction of medication use patterns in cardiometabolic disease

No authors listed. Nat Med. 2023 Jan.
No abstract available

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Comment on

  • Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases.
    Kiiskinen T, Helkkula P, Krebs K, Karjalainen J, Saarentaus E, Mars N, Lehisto A, Zhou W, Cordioli M, Jukarainen S, Rämö JT, Mehtonen J, Veerapen K, Räsänen M, Ruotsalainen S, Maasha M; FinnGen; Niiranen T, Tuomi T, Salomaa V, Kurki M, Pirinen M, Palotie A, Daly M, Ganna A, Havulinna AS, Milani L, Ripatti S. Kiiskinen T, et al. Nat Med. 2023 Jan;29(1):209-218. doi: 10.1038/s41591-022-02122-5. Epub 2023 Jan 18. Nat Med. 2023. PMID: 36653479 Free PMC article.

References

    1. James, S. L. et al. Global, regional, and national incidence, prevalence, and years lived with disability for 354 diseases and injuries for 195 countries and territories, 1990–2017: a systematic analysis for the Global Burden of Disease Study 2017. Lancet 392, 1789–1858 (2018). A review article that presents global burden of 354 disease including cardiovascular diseases. - DOI
    1. Marenberg, M. E., Risch, N., Berkman, L. F., Floderus, B. & de Faire, U. Genetic susceptibility to death from coronary heart disease in a study of twins. New Engl. J. Med. 330, 1041–1046 (1994). This paper reports heritability estimates for coronary heart disease. - DOI
    1. SEARCH Collaborative Group. SLCO1B1 variants and statin-induced myopathy—a genomewide study. New Engl. J. Med. 359, 789–799 (2008). A review article that presents evidence for adverse reactions to statin use for individuals carrying risk variants in the SLCO1B1 gene. - DOI

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