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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">persmed</journal-id><journal-title-group><journal-title xml:lang="ru">Российский журнал персонализированной медицины</journal-title><trans-title-group xml:lang="en"><trans-title>Russian Journal for Personalized Medicine</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2782-3806</issn><issn pub-type="epub">2782-3814</issn><publisher><publisher-name>ФОНД АЛМАЗОВА</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.18705/2782-3806-2023-3-5-14-21</article-id><article-id custom-type="edn" pub-id-type="custom">AWYDDG</article-id><article-id custom-type="elpub" pub-id-type="custom">persmed-192</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ГЕНЕТИЧЕСКИЕ РИСКИ И ПРИЧИНЫ ЗАБОЛЕВАНИЙ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>GENETIC RISKS AND CAUSES OF DISEASES</subject></subj-group></article-categories><title-group><article-title>Персонализированная профилактика: возможности и ограничения оценки полигенного риска</article-title><trans-title-group xml:lang="en"><trans-title>Personalized prevention: possibilities and limitations of polygenic risk assessment</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Драпкина</surname><given-names>О. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Drapkina</surname><given-names>O. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Драпкина Оксана Михайловна, д.м.н., профессор, академик РАН, директор,</p><p>101990, Москва, Петроверигский пер., 10, стр. 3.</p></bio><bio xml:lang="en"><p>Drapkina Oksana M., Ph.D., prof., full member of RAS, Director,</p><p>10, bldg 3,  Petroverigsky Lane, Moscow, 101990.</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Лимонова</surname><given-names>А. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Limonova</surname><given-names>A. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Лимонова Алена Сергеевна, научный сотрудник лаборатории клиномики,</p><p>101990, Москва, Петроверигский пер., 10, стр. 3.</p></bio><bio xml:lang="en"><p>Limonova Alena S., research fellow of the clinomic laboratory, </p><p>10, bldg 3,  Petroverigsky Lane, Moscow, 101990.</p></bio><email xlink:type="simple">limonova-alena@yandex.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Гарбузова</surname><given-names>Е. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Garbuzova</surname><given-names>E. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Гарбузова Елизавета Владимировна, лаборант-исследователь лаборатории клиномики, </p><p>101990, Москва, Петроверигский пер., 10, стр. 3.</p></bio><bio xml:lang="en"><p>Garbuzova Elizaveta V., laboratory assistant of the clinomic laboratory, </p><p>10, bldg 3,  Petroverigsky Lane, Moscow, 101990.</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Мешков</surname><given-names>А. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Meshkov</surname><given-names>A. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Мешков Алексей Николаевич, д.м.н., руководитель Института персонализированной терапии и профилактики, </p><p>101990, Москва, Петроверигский пер., 10, стр. 3.</p></bio><bio xml:lang="en"><p>Meshkov Alexey N., Ph.D., head of the institute of personalized therapy and prevention,</p><p>10, bldg 3,  Petroverigsky Lane, Moscow, 101990.</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ершова</surname><given-names>А. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Ershova</surname><given-names>A. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Ершова Александра Игоревна, д.м.н., заместитель директора по фундаментальной науке, руководитель лаборатории клиномики, </p><p>101990, Москва, Петроверигский пер., 10, стр. 3.</p></bio><bio xml:lang="en"><p>Ershova Alexandra I., Ph.D., head of the clinomic laboratory, deputy director for fundamental science,</p><p>10, bldg 3,  Petroverigsky Lane, Moscow, 101990.</p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Федеральное государственное бюджетное учреждение «Национальный медицинский&#13;
исследовательский центр терапии и профилактической медицины» Министерства&#13;
здравоохранения Российской Федерации</institution><country>Россия</country></aff><aff xml:lang="en"><institution>National Medical Research Center for Therapy and Preventive Medicine</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2023</year></pub-date><pub-date pub-type="epub"><day>22</day><month>11</month><year>2023</year></pub-date><volume>3</volume><issue>5</issue><fpage>14</fpage><lpage>21</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Драпкина О.М., Лимонова А.С., Гарбузова Е.В., Мешков А.Н., Ершова А.И., 2023</copyright-statement><copyright-year>2023</copyright-year><copyright-holder xml:lang="ru">Драпкина О.М., Лимонова А.С., Гарбузова Е.В., Мешков А.Н., Ершова А.И.</copyright-holder><copyright-holder xml:lang="en">Drapkina O.M., Limonova A.S., Garbuzova E.V., Meshkov A.N., Ershova A.I.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://persmed.elpub.ru/jour/article/view/192">https://persmed.elpub.ru/jour/article/view/192</self-uri><abstract><p>Хронические неинфекционные заболевания (ХНИЗ) составляют основную долю в структуре смертности во всем мире, при этом многие из них имеют многофакторную этиологию, включающую генетические факторы. В связи с этим в рамках создания индивидуальных стратегий профилактики ХНИЗ представляется перспективным проведение генетического тестирования с оценкой полигенного риска с помощью шкал генетического риска (ШГР). В настоящем обзоре будут рассмотрены ШГР различных ХНИЗ, их особенности и возможности применения.</p></abstract><trans-abstract xml:lang="en"><p>Noncommunicable diseases (NCDs) are the leading cause of mortality worldwide, with a vast majority of them having a multifactorial etiology, including genetics. That is why implementation of polygenic risk scores (PRS) in clinical practice with the aim of development of individual strategies for NCDs prevention seems promising. In this review we will discuss development and possible implications of PRSs.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>артериальная гипертензия</kwd><kwd>атеросклероз</kwd><kwd>гиперлипидемия</kwd><kwd>ишемическая болезнь сердца</kwd><kwd>ожирение</kwd><kwd>профилактика</kwd><kwd>сахарный диабет 2 типа</kwd><kwd>хронические неинфекционные заболевания</kwd><kwd>шкала генетического риска</kwd></kwd-group><kwd-group xml:lang="en"><kwd>atherosclerosis</kwd><kwd>coronary artery disease</kwd><kwd>hyperlipidemia</kwd><kwd>hypertension</kwd><kwd>noncommunicable diseases</kwd><kwd>obesity</kwd><kwd>polygenic risk score</kwd><kwd>prevention</kwd><kwd>type 2 diabetes mellitus</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Noncommunicable diseases. Global Health Estimates: Life expectancy and leading causes of death and disability. https://www.who.int/data/gho/data/themes/topics/topic-details/GHO/ncd-mortality (22 August 2023).</mixed-citation><mixed-citation xml:lang="en">Noncommunicable diseases. Global Health Estimates: Life expectancy and leading causes of death and disability. https://www.who.int/data/gho/data/themes/topics/topic-details/GHO/ncd-mortality (22 August 2023).</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Копылова О.В., Ершова А.И., Мешков А.Н., Драпкина О.М. Профилактика сердечно-сосудистых заболеваний на протяжении жизни. Часть 1: преконцепционный, пренатальный и грудной периоды. КВТиП. 2020;19(6):2647.</mixed-citation><mixed-citation xml:lang="en">Kopylova OV, Ershova AI, Meshkov AN, et al. Lifelong prevention of cardiovascular disease. Part I: preconceptional, prenatal and infant periods of life. Cardiovascular Therapy and Prevention. 2020;19(6):2647. (In Russian)</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Lewis C, Vassos E. Polygenic risk scores: from research tools to clinical instruments. Genome Med. 2020;12(1):44. DOI:10.1186/s13073-020-00742-5.</mixed-citation><mixed-citation xml:lang="en">Lewis C, Vassos E. Polygenic risk scores: from research tools to clinical instruments. Genome Med. 2020;12(1):44. DOI:10.1186/s13073-020-00742-5.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Choi SW, Mak TSH, O’Reilly PF. Tutorial: a guide to performing polygenic risk score analyses. Nat Protoc. 2020;15(9):2759–2772.</mixed-citation><mixed-citation xml:lang="en">Choi SW, Mak TSH, O’Reilly PF. Tutorial: a guide to performing polygenic risk score analyses. Nat Protoc. 2020;15(9):2759–2772.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Franzago M, Santurbano D, Vitacolonna E, Stuppia L. Genes and Diet in the Prevention of Chronic Diseases in Future Generations. Int J Mol Sci. 2020;21(7).</mixed-citation><mixed-citation xml:lang="en">Franzago M, Santurbano D, Vitacolonna E, Stuppia L. Genes and Diet in the Prevention of Chronic Diseases in Future Generations. Int J Mol Sci. 2020;21(7).</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Мешков А.Н., Щербакова Н.В. Молекулярно-генетическая диагностика предрасположенности к развитию ишемической болезни сердца: современное состояние проблемы. Consilium Medicum. 2016;18:22–26.</mixed-citation><mixed-citation xml:lang="en">Meshkov AN, Shcherbakova NV. Molecular genetic diagnosis of predisposition to the development of coronary heart disease: modern state of the problem. Consilium Medicum. 2016;18:22–26. (In Russian)</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Inouye M, Abraham G, Nelson CP, et al. Genomic Risk Prediction of Coronary Artery Disease in 480,000 Adults: Implications for Primary Prevention. J Am Coll Cardiol. 2018;72(16):1883–1893.</mixed-citation><mixed-citation xml:lang="en">Inouye M, Abraham G, Nelson CP, et al. Genomic Risk Prediction of Coronary Artery Disease in 480,000 Adults: Implications for Primary Prevention. J Am Coll Cardiol. 2018;72(16):1883–1893.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Khera AV, Chaffin M, Aragam KG, et al. Genomewide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations. Nat Genet. 2018;50(9):1219–1224.</mixed-citation><mixed-citation xml:lang="en">Khera AV, Chaffin M, Aragam KG, et al. Genomewide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations. Nat Genet. 2018;50(9):1219–1224.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Khera AV, Emdin CA, Drake I, et al. Genetic Risk, Adherence to a Healthy Lifestyle, and Coronary Disease. N Engl J Med. 2016;375(24):2349–2358.</mixed-citation><mixed-citation xml:lang="en">Khera AV, Emdin CA, Drake I, et al. Genetic Risk, Adherence to a Healthy Lifestyle, and Coronary Disease. N Engl J Med. 2016;375(24):2349–2358.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Hasbani NR, Ligthart S, Brown MR, et al. American Heart Association’s Life’s Simple 7: Lifestyle Recommendations, Polygenic Risk, and Lifetime Risk of Coronary Heart Disease. Circulation. 2022;145(11):808–818.</mixed-citation><mixed-citation xml:lang="en">Hasbani NR, Ligthart S, Brown MR, et al. American Heart Association’s Life’s Simple 7: Lifestyle Recommendations, Polygenic Risk, and Lifetime Risk of Coronary Heart Disease. Circulation. 2022;145(11):808–818.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Klarin D, Damrauer SM, Tsao PS, et al. Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program. Circulation. 2020;142(17):1633–1646.</mixed-citation><mixed-citation xml:lang="en">Klarin D, Damrauer SM, Tsao PS, et al. Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program. Circulation. 2020;142(17):1633–1646.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Natarajan P, Young R, Stitziel NO, et al. Polygenic Risk Score Identifies Subgroup With Higher Burden of Atherosclerosis and Greater Relative Benefit From Statin Therapy in the Primary Prevention Setting. Circulation. 2017;135(22):2091–2101.</mixed-citation><mixed-citation xml:lang="en">Natarajan P, Young R, Stitziel NO, et al. Polygenic Risk Score Identifies Subgroup With Higher Burden of Atherosclerosis and Greater Relative Benefit From Statin Therapy in the Primary Prevention Setting. Circulation. 2017;135(22):2091–2101.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">den Hoed M, Strawbridge RJ, Almgren P, et al. GWASidentified loci for coronary heart disease are associated with intima-media thickness and plaque presence at the carotid artery bulb. Atherosclerosis. 2015;239(2):304–310.</mixed-citation><mixed-citation xml:lang="en">den Hoed M, Strawbridge RJ, Almgren P, et al. GWASidentified loci for coronary heart disease are associated with intima-media thickness and plaque presence at the carotid artery bulb. Atherosclerosis. 2015;239(2):304–310.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">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.</mixed-citation><mixed-citation xml:lang="en">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.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Futema M, Taylor-Beadling A, Williams M, et al. Genetic testing for familial hypercholesterolemia-past, present, and future. J Lipid Res. 2021;62:100139.</mixed-citation><mixed-citation xml:lang="en">Futema M, Taylor-Beadling A, Williams M, et al. Genetic testing for familial hypercholesterolemia-past, present, and future. J Lipid Res. 2021;62:100139.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Trinder M, Paquette M, Cermakova L, et al. Polygenic Contribution to Low-Density Lipoprotein Cholesterol Levels and Cardiovascular Risk in Monogenic Familial Hypercholesterolemia. Circ Genomic Precis Med. 2020;13(5):515–523.</mixed-citation><mixed-citation xml:lang="en">Trinder M, Paquette M, Cermakova L, et al. Polygenic Contribution to Low-Density Lipoprotein Cholesterol Levels and Cardiovascular Risk in Monogenic Familial Hypercholesterolemia. Circ Genomic Precis Med. 2020;13(5):515–523.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Marston NA, Kamanu FK, Nordio F, et al. Predicting Benefit FromEvolocumab Therapy in Patients With Atherosclerotic Disease Using a Genetic Risk Score: Results From the FOURIER Trial. Circulation. 2020;141(8):616–623.</mixed-citation><mixed-citation xml:lang="en">Marston NA, Kamanu FK, Nordio F, et al. Predicting Benefit FromEvolocumab Therapy in Patients With Atherosclerotic Disease Using a Genetic Risk Score: Results From the FOURIER Trial. Circulation. 2020;141(8):616–623.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Vanhoye X, Bardel C, Rimbert A, et al. A new 165-SNP low-density lipoprotein cholesterol polygenic risk score based on next generation sequencing outperforms previously published scores in routine diagnostics of familial hypercholesterolemia. Transl Res. 2023;255:119–127.</mixed-citation><mixed-citation xml:lang="en">Vanhoye X, Bardel C, Rimbert A, et al. A new 165-SNP low-density lipoprotein cholesterol polygenic risk score based on next generation sequencing outperforms previously published scores in routine diagnostics of familial hypercholesterolemia. Transl Res. 2023;255:119–127.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Лимонова А.С., Ершова А.И., Киселева А.В. и др. Оценка полигенного риска артериальной гипертензии. Кардиоваскулярная терапия и профилактика. 2022;21(12):3464.</mixed-citation><mixed-citation xml:lang="en">Limonova AS, Ershova AI, Kiseleva AV, et al. Assessment of polygenic risk of hypertension. Kardiovaskulyarnaya terapiya i profilaktika. 2022;21(12):3464. (In Russian)</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Giontella A, Sjögren M, Lotta LA, et al. Clinical Evaluation of the Polygenetic Background of Blood Pressure in the PopulationBased Setting. Hypertension. 2020;77:169–77.</mixed-citation><mixed-citation xml:lang="en">Giontella A, Sjögren M, Lotta LA, et al. Clinical Evaluation of the Polygenetic Background of Blood Pressure in the PopulationBased Setting. Hypertension. 2020;77:169–77.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Vaura F, Kauko A, Suvila K, et al. Polygenic risk scores predict hypertension onset and cardiovascular risk. Hypertension. 2021:1119–27.</mixed-citation><mixed-citation xml:lang="en">Vaura F, Kauko A, Suvila K, et al. Polygenic risk scores predict hypertension onset and cardiovascular risk. Hypertension. 2021:1119–27.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Sun X, Pan Y, Zhang R, et al. Life-Course Associations between Blood Pressure-Related Polygenic Risk Scores and Hypertension in the Bogalusa Heart Study. Genes (Basel). 2022;13(8).</mixed-citation><mixed-citation xml:lang="en">Sun X, Pan Y, Zhang R, et al. Life-Course Associations between Blood Pressure-Related Polygenic Risk Scores and Hypertension in the Bogalusa Heart Study. Genes (Basel). 2022;13(8).</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Malik R, Chauhan G, Traylor M, et al. Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. Nat Genet. 2018;50(4):524–537.</mixed-citation><mixed-citation xml:lang="en">Malik R, Chauhan G, Traylor M, et al. Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. Nat Genet. 2018;50(4):524–537.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Rutten-Jacobs LC, Larsson SC, Malik R, et al. Genetic risk, incident stroke, and the benefits of adhering to a healthy lifestyle: cohort study of 306473 UK Biobank participants. BMJ. 2018;363:k4168.</mixed-citation><mixed-citation xml:lang="en">Rutten-Jacobs LC, Larsson SC, Malik R, et al. Genetic risk, incident stroke, and the benefits of adhering to a healthy lifestyle: cohort study of 306473 UK Biobank participants. BMJ. 2018;363:k4168.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Marston NA, Patel PN, Kamanu FK, et al. Clinical Application of a Novel Genetic Risk Score for Ischemic Stroke in Patients With Cardiometabolic Disease. Circulation. 2021;143(5):470–478.</mixed-citation><mixed-citation xml:lang="en">Marston NA, Patel PN, Kamanu FK, et al. Clinical Application of a Novel Genetic Risk Score for Ischemic Stroke in Patients With Cardiometabolic Disease. Circulation. 2021;143(5):470–478.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Khera AV, Chaffin M, Aragam KG, et al. Genomewide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations. Nat Genet. 2018;50(9):1219–1224.</mixed-citation><mixed-citation xml:lang="en">Khera AV, Chaffin M, Aragam KG, et al. Genomewide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations. Nat Genet. 2018;50(9):1219–1224.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Yun JS, Jung SH, Shivakumar M, et al. Polygenic risk for type 2 diabetes, lifestyle, metabolic health, and cardiovascular disease: a prospective UK Biobank study. Cardiovasc Diabetol 21, 131 (2022).</mixed-citation><mixed-citation xml:lang="en">Yun JS, Jung SH, Shivakumar M, et al. Polygenic risk for type 2 diabetes, lifestyle, metabolic health, and cardiovascular disease: a prospective UK Biobank study. Cardiovasc Diabetol 21, 131 (2022).</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Ge T, Irvin MR, Patki A, et al. Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populationns. Genome Med 14, 70 (2022).</mixed-citation><mixed-citation xml:lang="en">Ge T, Irvin MR, Patki A, et al. Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populationns. Genome Med 14, 70 (2022).</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Li JH, Szczerbinski L, Dawed AY, et al. A polygenic score for type 2 diabetes risk is associated with both the acute and sustained response to sulfonylureas. Diabetes. 2021;70:293–300.</mixed-citation><mixed-citation xml:lang="en">Li JH, Szczerbinski L, Dawed AY, et al. A polygenic score for type 2 diabetes risk is associated with both the acute and sustained response to sulfonylureas. Diabetes. 2021;70:293–300.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Finer N. Medical consequences of obesity. Medicine. 2015;43(2):88–93.</mixed-citation><mixed-citation xml:lang="en">Finer N. Medical consequences of obesity. Medicine. 2015;43(2):88–93.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Khera AV, Chaffin M, Wade KH, et al. Polygenic Prediction of Weight and Obesity Trajectories from Birth to Adulthood. Cell. 2019 Apr 18;177(3):587–596.e9.</mixed-citation><mixed-citation xml:lang="en">Khera AV, Chaffin M, Wade KH, et al. Polygenic Prediction of Weight and Obesity Trajectories from Birth to Adulthood. Cell. 2019 Apr 18;177(3):587–596.e9.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Dashti HS, Miranda N, Cade BE, et al. Interaction of obesity polygenic score with lifestyle risk factors in an electronic health record biobank. BMC Med 20, 5 (2022).</mixed-citation><mixed-citation xml:lang="en">Dashti HS, Miranda N, Cade BE, et al. Interaction of obesity polygenic score with lifestyle risk factors in an electronic health record biobank. BMC Med 20, 5 (2022).</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Dudbridge F. Power and predictive accuracy of polygenic risk scores. PLoS Genet. 2013;9(3):e1003348.</mixed-citation><mixed-citation xml:lang="en">Dudbridge F. Power and predictive accuracy of polygenic risk scores. PLoS Genet. 2013;9(3):e1003348.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Manolio TA, Collins FS, Cox NJ, et al. Finding the missing heritability of complex diseases. Nature. 2009;461(7265):747.</mixed-citation><mixed-citation xml:lang="en">Manolio TA, Collins FS, Cox NJ, et al. Finding the missing heritability of complex diseases. Nature. 2009;461(7265):747.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Igo RP, Kinzy TG, Cooke Bailey JN. Genetic Risk Scores. CurrProtoc Hum Genet. 2019;104(1):e95.</mixed-citation><mixed-citation xml:lang="en">Igo RP, Kinzy TG, Cooke Bailey JN. Genetic Risk Scores. CurrProtoc Hum Genet. 2019;104(1):e95.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Martin AR, Gignoux CR, Walters RK, et al. Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations. Am J Hum Genet. 2017;100(4):635.</mixed-citation><mixed-citation xml:lang="en">Martin AR, Gignoux CR, Walters RK, et al. Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations. Am J Hum Genet. 2017;100(4):635.</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Dron JS, Hegele RA. The evolution of geneticbased risk scores for lipids and cardiovascular disease. CurrOpinLipidol. 2019;30(2):71–81.</mixed-citation><mixed-citation xml:lang="en">Dron JS, Hegele RA. The evolution of geneticbased risk scores for lipids and cardiovascular disease. CurrOpinLipidol. 2019;30(2):71–81.</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Wand H, Lambert SA, Tamburro C, et al. Improving reporting standards for polygenic scores in risk prediction studies. Nature. 2021;591(7849):211–219.</mixed-citation><mixed-citation xml:lang="en">Wand H, Lambert SA, Tamburro C, et al. Improving reporting standards for polygenic scores in risk prediction studies. Nature. 2021;591(7849):211–219.</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
