1. Martin SS, Aday AW, Almarzooq ZI, Anderson CAM, Arora P, Avery CL, et al. 2024 Heart Disease and Stroke Statistics: A Report of US and Global Data From the American Heart Association. Circulation. 2024;l49(8):e347-e913. DOI: 10.1161/CIR.0000000000001209
2. Visseren FLJ, Mach F, Smulders YM, Carballo D, Koskinas KC, Bdck M, et al. 2021 ESC Guidelines on cardiovascular disease prevention in clinical practice. Eur Heart J. 2021;42(34):3227-3337. DOI: 10.1093/eurheartj/ehab484
3. Martin SS, Sperling LS, Blaha MJ, Wilson PWF, Gluckman TJ, Blumenthal RS, Stone NJ. Clinician-patient risk discussion for atherosclerotic cardiovascular disease prevention: importance to implementation of the 2013 ACC/AHA Guidelines. J Am Coll Cardiol. 2015;65(13):1361-1368. DOI: 10.1016/j.jacc.2015.01.043
4. Ezhov MV, Kukharchuk VV, Sergienko IV, et al. Disorders of lipid metabolism. Clinical Guidelines 2023- Russian Journal of Cardiology. 2023;28(5):5471. In Russian.
Клинические рекомендации. Нарушения липидного обмена. МЗ РФ, 2023. DOI: 10.15829/1560-4071-2023-5471
5. Yanai H, Yoshida H. Secondary dyslipidemia: its treatments and association with atherosclerosis. Glob Health Med. 2021;3(1):15-23. DOI: 10.35772/ghm.2020.01078
6. Mach F, Baigent C, Catapano AL, Koskinas KC, Casula M, Badimon L, et al. 2019 ESC/EAS Guidelines for the management of dyslipidaemias: lipid modification to reduce cardiovascular risk. Eur Heart J. 2020;41(1):111-188. DOI: 10.1093/eurheartj/ehz455
7. Tandirerung FJ. The Clinical Importance of Differentiating Monogenic Familial Hypercholesterolemia from Polygenic Hypercholesterolemia. Curr Cardiol Rep. 2022;24(11):1669-1677. DOI: 10.1007/s11886-022-01783-5
8. Taylor A, Wang D, Patel K, Whittall R, Wood G, Farrer M, et al. Mutation detection rate and spectrum in familial hypercholesterolaemia patients in the UK pilot cascade project. Clin Genet. 2010;77(6):572-580. DOI: 10.1111/j.1399-0004.2009.01356.x
9. D’Erasmo L, Minicocci I, Nicolucci A, Pintus P, Roeters Van Lennep JE, et al. Autosomal Recessive Hypercholesterolemia: Long-Term Cardiovascular Outcomes. J Am Coll Cardiol. 2018;71ß):279-288. DOI: 10.1016/j.jacc.2017.11.028
10. Futema M, Shah S, Cooper JA, Li K, Whittall RA, Sharifi M, et al. Refinement of variant selection for the LDL cholesterol genetic risk score in the diagnosis of the polygenic form of clinical familial hypercholesterolemia and replication in samples from 6 countries. Clin Chem. 2015;61(1):231-238. DOI: 10.1373/clinchem.2014.231365
11. Talmud PJ, Shah S, Whittall R, Futema M, Howard P, Cooper JA, et al. Use of low-density lipoprotein cholesterol gene score to distinguish patients with polygenic and monogenic familial hypercholesterolaemia: a case-control study. Lancet. 2013;381(9874):1293-1301. DOI: 10.1016/S0140-6736(12)62127-8
12. Langsted A, Nordestgaard BG. Lipoprotein(a) as Part of the Diagnosis of Clinical Familial Hypercholesterolemia. Curr Atheroscler Rep. 2022;24(4):289-296. DOI: 10.1007/s11883-022-01002-0
13. Fredrickson DS, Lees RS. A system for phenotyping hyperlipoproteinemia. Circulation. 1965;31:321-327. DOI: 10.1161/01.cir.31.3.321
14. Ballout RA, Remaley AT. Chapter 28. Pediatric dyslipidemias: lipoprotein metabolism disorders in children. Editors: D. Dietzen, M. Bennett, E. Wong, S. Haymond. Biochemical and Molecular Basis of Pediatric Disease (5th Ed.). Academic Press, 2021:965-1022. DOI: 10.1016/B978-0-12-817962-8.00002-0
15. Myant NB. Familial defective apolipoprotein B-100: a review, including some comparisons with familial hypercholesterolaemia. Atherosclerosis. 1993;104(1-2):1-18. DOI: 10.1016/0021-9150(93)90171-p
16. Meshkov AN, Ershova AI, Shcherbakova NV, Rozhkova TA, Kalinina MV, Kukharchuk VV, Boytsov SA. Phenotypical features of heterozygous familial hypercholesterolemia in individuals with LDLR or APOB gene mutations. Cardiovascular Therapy and Prevention. 2011;10(8):63-65. In Russian.
Мешков А Н, Ершова А.И, Щербакова Н.В., Рожкова ТА, Калинина М.В., Кухарчук В.В., Бойцов С.А. Фенотипические особенности течения гетерозиготной формы семейной гиперхолестеринемии у носителей мутаций генов LDLR и APOB. Кардиоваскулярная терапия и профилактика. 2011;10(8):63-65).
17. Toft-Nielsen F, Emanuelsson F, Benn M. Familial Hypercholesterolemia Prevalence Among Ethnicities-Systematic Review and Meta-Analysis. Front Genet. 2022;13:840797. DOI: 10.3389/fgene.2022.840797
18. Beheshti SO, Madsen CM, Varbo A, Nordestgaard BG. Worldwide Prevalence of Familial Hypercholesterolemia: MetaAnalyses of 11 Million Subjects. J Am Coll Cardiol. 2020;75(20):2553-2566. DOI: 10.1016/j.jacc.2020.03057
19. Berberich AJ, Hegele R.A. The complex molecular genetics of familial hypercholesterolaemia. Nat Rev Cardiol. 2019;16(1):9-20. DOI: 10.1038/s41569-018-0052-6
20. Meshkov AN, Ershova AI, Kiseleva AV, Shalnova SA, Drapkina OM, Boytsov SA, On Behalf Of The Fh-Esse-Rf Investigators. The Prevalence of Heterozygous Familial Hypercholesterolemia in Selected Regions of the Russian Federation: The FH-ESSE-RF Study. J Pers Med. 2021;11(6):464. DOI: 10.3390/jpm11060464
21. Futema M, Bourbon M, Williams M, Humphries SE. Clinical utility of the polygenic LDL-C SNP score in familial hypercholesterolemia. Atherosclerosis. 2018;277:457-463. DOI: 10.1016/j.atherosclerosis.2018.06.006
22. Shakhtshneider E, Ivanoshchuk D, Timoshchenko O, Orlov P, Semaev S, Valeev E, et al. Analysis of Rare Variants in Genes Related to Lipid Metabolism in Patients with Familial Hypercholesterolemia in Western Siberia (Russia). J Pers Med. 2021;11(11):1232. DOI: 10.3390/jpm11111232
23. Vasilyev VB, Zakharova FM, Bogoslovskaya TY, Mandelshtam MY. Analysis of the low density lipoprotein receptor gene (LDLR) mutation spectrum in Russian familial hypercholesterolemia. Vavilovskii Zhurnal Genet Selektsii. 2022;26(3):319-326. DOI: 10.18699/VJGB-22-38
24. Meshkov A, Ershova A, Kiseleva A, Zotova E, Sotnikova E, Petukhova A, et al. The LDLR, APOB, and PCSK9 Variants of Index Patients with Familial Hypercholesterolemia in Russia. Genes (Basel). 2021;12(1):66. DOI: 10.3390/genes12010066
25. Brænne I, Kleinecke M, Reiz B, Graf E, Strom T, Wieland T, et al. Systematic analysis of variants related to familial hypercholesterolemia in families with premature myocardial infarction. Eur J Hum Genet. 2016;24(2):191-197. DOI: 10.1038/ejhg.2015.100
26. Trinder M, Li X, DeCastro ML, Cermakova L, Sadananda S, Jackson LM, et al. Risk of Premature Atherosclerotic Disease in Patients With Monogenic Versus Polygenic Familial Hypercholesterolemia. J Am Coll Cardiol. 2019;74(4):512-522. DOI: 10.1016/j.jacc.2019.05.043
27. Henderson R, O’Kane M, McGilligan V, Watterson S. The genetics and screening of familial hypercholesterolaemia. J Biomed Sci. 2016;23:39-. DOI: 10.1186/s12929-016-0256-1
28. Trinder M, Francis GA, Brunham LR. Association of Monogenic vs Polygenic Hypercholesterolemia With Risk of Atherosclerotic Cardiovascular Disease. JAMA Cardiol. 2020;5(4):390-399. DOI: 10.1001/jamacardio.2019.5954
29. Rogozhina A A, Averkova AO, Zubova EA, Minushkina LO, Brazhnik VA, Ivanova ON, et al. Incidence of familial hypercholesterolemia in patients with early manifestations of coronary artery disease: data from a Russian multicenter study and meta-analysis.Russian Journal of Cardiology. 2023;28(10):5587. In Russian.
Рогожина А.А., Аверкова А.О, Зубова Е.А., Минушкина Л.О., Бражник В.А., Иванова ОН. и др. Частота встречаемости семейной гиперхолестеринемии у больных с ранней манифестацией ишемической болезни сердца: данные российского многоцентрового исследования и метаанализ. Российский кардиологический журнал. 2023;28(10):5587). DOI: 10.15829/1560-4071-20235587
30. National Organization for Rare Disorders Familial hypercholesterolemia. https://rarediseases.org/rare-diseases/familial-hypercholesterolemia/Date: 2023.
31. Singh K, Prabhakaran D. Apolipoprotein B. An ideal biomarker for atherosclerosis? Indian Heart J. 2024;76(Suppl 1):S121-S129. DOI: 10.1016/j.ihj.2023.12.001
32. Huang Y, Chen S, Pan H, Yang S, Cheng W. Relationship between serum apolipoprotein B and risk of all-cause and cardiovascular disease mortality in individuals with hypertension: a prospective cohort study. BMC Cardiovasc Disord. BMC Cardiovasc Disord. 2024;24(1):273.