Abstract
Lysosomal acid lipase deficiency (LAL-D) is a monogenic progressive life-threatening condition characterized by abnormal lipid profiles in most patients of all ages. Timely diagnosis and early pathogenetically-oriented treatment (available in Russia) are crucial for children and young adults since abnormal serum levels of lipids are associated with the onset and severity of atherosclerosis in adolescence, young and middle age. The prognosis of LAL-D without pathogenetically oriented treatment is poor. Data on cholesteryl ester storage disease (a variant of LAL-D in children and adults), early atherosclerosis, coronary heart disease, aortic calcification, etc., are available. However, early diagnosis of LAL-D is difficult due to long-term latent course and nonspecific clinical signs. In December 2020, a panel of leading Russian experts in the diagnosis and treatment of orphan diseases and lipidologists was held in Moscow. This panel developed an algorithm to optimize the early diagnosis of dyslipidemias in children and young adults and identify patients with LAL-D in a total population of patients with lipid profile abnormalities. KEYWORDS: lysosomal acid lipase deficiency, lipid profile, atherosclerosis, lipid center. FOR CITATION: Ezhov M.V., Zakharova E.Yu., Avramenko A.A. et al. Timely diagnosis of lysosomal acid lipase deficiency in children and young adults with lipid profile abnormalities. Expert opinion. Russian Journal of Woman and Child Health. 2021;4(3):268–276 (in Russ.). DOI: 10.32364/2618-8430-2021-4-3-268-276.
Highlights
Обзоры children and adults), early atherosclerosis, coronary heart disease, aortic calcification, etc., are available
In December 2020, a panel of leading Russian experts in the diagnosis and treatment of orphan diseases and lipidologists was held in Moscow. This panel developed an algorithm to optimize the early diagnosis of dyslipidemias in children and young adults and identify patients with LAL-D in a total population of patients with lipid profile abnormalities
(Med.), Professor of the RAS, Head of the Department of Pediatric Gastroenterology, Hepatology, and Dietetics, Federal Research Center for Nutrition and Biotechnology; 2/14, Ust'inskiy pass., Moscow, 109240, Russian Federation; Head of the Department of Gastroenterology and Dietetics of the Faculty of Additional Professional Education, Pirogov Russian National Research Medical University; 1, Ostrovityanov str., Moscow, 117437, Russian Federation; ORCID iD 0000-0002-0762-0873
Summary
Вопросы своевременной диагностики дефицита лизосомной кислой липазы у детей и молодых взрослых с нарушениями липидного профиля. РЕЗЮМЕ Дефицит лизосомной кислой липазы (ДЛКЛ) является моногенным жизнеугрожающим и прогрессирующим заболеванием, сопровождающимся нарушениями липидного профиля у подавляющего количества пациентов всех возрастов. Своевременная диагностика и раннее начало доступной в РФ патогенетической терапии данного заболевания особенно актуальны для детей и молодых взрослых, так как аномальные уровни липидов в сыворотке крови в детстве ассоциированы с дебютом и степенью тяжести атеросклероза в подростковом, молодом и зрелом возрасте. В Москве состоялся Совет экспертов при участии ведущих российских липидологов и специалистов с опытом диагностики и лечения орфанных заболеваний. Был разработан алгоритм действий по оптимизации ранней диагностики дислипидемий у детей и молодых взрослых и выявлению пациентов с ДЛКЛ среди общего числа пациентов с нарушениями липидного профиля. ДЛЯ ЦИТИРОВАНИЯ: Ежов М.В., Захарова Е.Ю., Авраменко А.А.
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