CORONARY ANGIOGRAPHY IN PATIENTS WITH PREMATURE ACUTE CORONARY SYNDROME AND FAMILY HYPERCHOLESTEROLEMIA

A O Averkova , V A Brazhnik , O S Koroleva , E A Zubova , D S Sizgunov , A A Rogozhina , D A Zateyshchikov

Journal of Clinical Practice ›› 2017, Vol. 8 ›› Issue (3) : 34 -41.

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Journal of Clinical Practice ›› 2017, Vol. 8 ›› Issue (3) : 34 -41. DOI: 10.17816/clinpract8334-41
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CORONARY ANGIOGRAPHY IN PATIENTS WITH PREMATURE ACUTE CORONARY SYNDROME AND FAMILY HYPERCHOLESTEROLEMIA

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Abstract

Familial hypercholesterolemia (FH) is an autosomal dominant genetic disorder with a prevalence of 1/200-1/500 in the general population. The aim of the study was to assess the specific features of coronary angiography in young patients with acute coronary syndrome (ACS) and FH diagnosed using Dutch Lipid Clinic Network (I) and Simone Broome Register (II) criteria. 224 pts with early onset of ACS who underwent coronary angiography were selected (≤ 55 years of age for men and ≤ 60 years of age for women). Two, three vessel disease/left coronary artery (LCA) impairment was observed in 12 of 13 (92,3%) pts with definite/possible FH (I, p=0,036) and in 28 of 29 (96,6%) pts with probable FH (II, p=0,001). In patients with family history of cardiovascular disease three ves-sel disease or LCA impairment was observed in 54 of 73 (74%) pts (p=0,024). Comparing two groups of patients with LDL over and below 4,6 mmol/l (the concentration was obtained by ROC analysis) it was shown that 20 of 29 (69%) and 58 of 144 (40,3%) pts (p=0,036) respectively had culprit vessel thrombosis. Thus, we can suppose that in pts with higher LDL level atherosclerotic plaque rupture is observed more frequently in case of ACS. Therefore, it has been shown that multivessel and LCA stem impairment in young patients with ACS and FH is associated with both main factors used for not genetic FH diagnosis: high LDL cholesterol level and family history of cardiovascular disease.

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familial hypercholesterolemia / acute coronary syndrome

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A O Averkova, V A Brazhnik, O S Koroleva, E A Zubova, D S Sizgunov, A A Rogozhina, D A Zateyshchikov. CORONARY ANGIOGRAPHY IN PATIENTS WITH PREMATURE ACUTE CORONARY SYNDROME AND FAMILY HYPERCHOLESTEROLEMIA. Journal of Clinical Practice, 2017, 8(3): 34-41 DOI:10.17816/clinpract8334-41

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References

[1]

Nordestgaard B.G., Chapman M.J., Humphries S.E. et al. Familial hypercholesterolaemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease: consensus statement of the European Atherosclerosis Society. European heart journal 2013; 34(45):3478-3490a.

[2]

Корнева В.А., Кузнецова Т.Ю., Богословская Т.Ю. и др. Современные возможности диагностики гиперхолестеринемии до появления клинических проявлений атеросклероза. Атеросклероз и дислипидемии 2016; 1:22-32.

[3]

Соловьева Е. Ю., Ежов М.В., Шахнович Р.М. и др. Частота семейной гиперхолестеринемии у больных с ранним развитием острого коронарного синдрома. Тезисы Всероссийской научно-практической конференции «Кардиология 2017: лечить не болезнь, а больного» 2017; 43-44.

[4]

Nanchen D., Gencer B., Auer R. et al. Prevalence and management of familial hypercholesterolaemia in patients with acute coronary syndromes. European heart journal 2015; 36(36):2438-2445.

[5]

Аверкова А.О., Бражник В.А., Королева О.С. и др. Особенности течения острого коронарного синдрома у молодых больных с семейной гиперлипидемией по данным наблюдательного проекта Оракул II. Медицинский вестник Северного Кавказа 2017; 1:5-8.

[6]

Catapano A.L., Graham I., De Backer G. et al. 2016 ESC/EASGuidelinesforthe Managementof Dyslipidaemias. European heart journal 2016; 37(39):2999-3058.

[7]

Wierzbicki A.S., Humphries S.E., Minhas R. Familial hypercholesterolaemia: summary of NICE guidance. BMJ (Clinical research ed) 2008; 337:a1095.

[8]

Tada H., Kawashiri M.A., Okada H. etal. Assessment of coronary atherosclerosis in patients with familial hypercholesterolemia by coronary computed tomography angiography. Am J Cardiol 2015; 115(6):724-729.

[9]

Сергиенко И.В., Мартиросян Л.А. Перфузия миокарда левого желудочка у больных гиперхолестеринемией на фоне терапии статинами. Атеросклероз и дислипидемии 2017; 2:38-47.

[10]

Nanchen D., Gencer B., Muller O., et al. Prognosis of Patients With Familial Hypercholesterolemia After Acute Coronary Syndromes. Circulation 2016, 134(10):698-709.

[11]

Besseling J., Kindt I., Hof M., et al. Severe heterozygous familial hypercholesterolemia and risk for cardiovascular disease: a study of a cohort of 14,000 mutation carriers. Atherosclerosis 2014; 233(1):219-223.

[12]

Rerup S.A., Bang L.E., Mogensen U.M. et al. The prevalence and prognostic importance of possible familial hypercholesterolemia in patients with myocardial infarction. Am Heart J 2016; 181:35-42.

[13]

Li J.J., Li S., Zhu C.G. et al. Familial Hypercholesterolemia Phenotype in Chinese Patients Undergoing Coronary Angiography. Arterioscler Thromb Vasc Biol 2017; 37(3):570-579.

[14]

Prajapati J., Joshi H., Sahoo S. et al. AGE-Related Differences of Novel Atherosclerotic Risk Factors and Angiographic Profile Among Gujarati Acute Coronary Syndrome Patients. Journal of clinical and diagnostic research: JCDR 2015; 9(6):Oc05-09.

[15]

Benn M., Watts G.F., Tybjaerg-Hansen A. et al. Mutations causative of familial hypercholesterolaemia: screening of 98 098 individuals from the Copenhagen General Population Study estimated a prevalence of 1 in European heart journal 2016; 37(17):1384-1394.

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Averkova A.O., Brazhnik V.A., Koroleva O.S., Zubova E.A., Sizgunov D.S., Rogozhina A.A., Zateyshchikov D.A.

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