Sitosterolemia: a review and update of pathophysiology, clinical spectrum, diagnosis, and management

Sitosterolemia is an autosomal recessive disorder characterized by increased plant sterol levels, xanthomas, and accelerated atherosclerosis. Although it was originally reported in patients with normolipemic xanthomas, severe hypercholesterolemia have been reported in patients with sitosterolemia, e...

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Main Author: Eun-Gyong Yoo
Format: Article
Language:English
Published: Korean Society of Pediatric Endocrinology 2016-03-01
Series:Annals of Pediatric Endocrinology & Metabolism
Subjects:
Online Access:http://e-apem.org/upload/pdf/apem-21-7.pdf
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author Eun-Gyong Yoo
author_facet Eun-Gyong Yoo
author_sort Eun-Gyong Yoo
collection DOAJ
description Sitosterolemia is an autosomal recessive disorder characterized by increased plant sterol levels, xanthomas, and accelerated atherosclerosis. Although it was originally reported in patients with normolipemic xanthomas, severe hypercholesterolemia have been reported in patients with sitosterolemia, especially in children. Sitosterolemia is caused by increased intestinal absorption and decreased biliary excretion of sterols resulting from biallelic mutations in either ABCG5 or ABCG8, which encode the sterol efflux transporter ABCG5 and ABCG8. Patients with sitosterolemia show extreme phenotypic heterogeneity, ranging from almost asymptomatic individuals to those with severe hypercholesterolemia leading to accelerated atherosclerosis and premature cardiac death. Hematologic manifestations include hemolytic anemia with stomatocytosis, macrothrombocytopenia, splenomegaly, and abnormal bleeding. The mainstay of therapy includes dietary restriction of both cholesterol and plant sterols and the sterol absorption inhibitor, ezetimibe. Foods rich in plant sterols include vegetable oils, wheat germs, nuts, seeds, avocado, shortening, margarine and chocolate. Hypercholesterolemia in patients with sitosterolemia is dramatically responsive to low cholesterol diet and bile acid sequestrants. Plant sterol assay should be performed in patients with normocholesterolemic xanthomas, hypercholesterolemia with unexpectedly good response to dietary modifications or to cholesterol absorption inhibitors, or hypercholesterolemia with poor response to statins, or those with unexplained hemolytic anemia and macrothrombocytopenia. Because prognosis can be improved by proper management, it is important to find these patients out and diagnose correctly. This review article aimed to summarize recent publications on sitosterolemia, and to suggest clinical indications for plant sterol assay.
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spelling doaj.art-d5aa61e00b1144f6b0477cc62fb7857d2022-12-22T00:41:27ZengKorean Society of Pediatric EndocrinologyAnnals of Pediatric Endocrinology & Metabolism2287-10122287-12922016-03-0121171410.6065/apem.2016.21.1.7648Sitosterolemia: a review and update of pathophysiology, clinical spectrum, diagnosis, and managementEun-Gyong Yoo0Department of Pediatrics, CHA Bundang Medical Center, CHA University, Seongnam, Korea.Sitosterolemia is an autosomal recessive disorder characterized by increased plant sterol levels, xanthomas, and accelerated atherosclerosis. Although it was originally reported in patients with normolipemic xanthomas, severe hypercholesterolemia have been reported in patients with sitosterolemia, especially in children. Sitosterolemia is caused by increased intestinal absorption and decreased biliary excretion of sterols resulting from biallelic mutations in either ABCG5 or ABCG8, which encode the sterol efflux transporter ABCG5 and ABCG8. Patients with sitosterolemia show extreme phenotypic heterogeneity, ranging from almost asymptomatic individuals to those with severe hypercholesterolemia leading to accelerated atherosclerosis and premature cardiac death. Hematologic manifestations include hemolytic anemia with stomatocytosis, macrothrombocytopenia, splenomegaly, and abnormal bleeding. The mainstay of therapy includes dietary restriction of both cholesterol and plant sterols and the sterol absorption inhibitor, ezetimibe. Foods rich in plant sterols include vegetable oils, wheat germs, nuts, seeds, avocado, shortening, margarine and chocolate. Hypercholesterolemia in patients with sitosterolemia is dramatically responsive to low cholesterol diet and bile acid sequestrants. Plant sterol assay should be performed in patients with normocholesterolemic xanthomas, hypercholesterolemia with unexpectedly good response to dietary modifications or to cholesterol absorption inhibitors, or hypercholesterolemia with poor response to statins, or those with unexplained hemolytic anemia and macrothrombocytopenia. Because prognosis can be improved by proper management, it is important to find these patients out and diagnose correctly. This review article aimed to summarize recent publications on sitosterolemia, and to suggest clinical indications for plant sterol assay.http://e-apem.org/upload/pdf/apem-21-7.pdfSitosterolemiaPhytosterolemiaHypercholesterolemiaPlant sterol
spellingShingle Eun-Gyong Yoo
Sitosterolemia: a review and update of pathophysiology, clinical spectrum, diagnosis, and management
Annals of Pediatric Endocrinology & Metabolism
Sitosterolemia
Phytosterolemia
Hypercholesterolemia
Plant sterol
title Sitosterolemia: a review and update of pathophysiology, clinical spectrum, diagnosis, and management
title_full Sitosterolemia: a review and update of pathophysiology, clinical spectrum, diagnosis, and management
title_fullStr Sitosterolemia: a review and update of pathophysiology, clinical spectrum, diagnosis, and management
title_full_unstemmed Sitosterolemia: a review and update of pathophysiology, clinical spectrum, diagnosis, and management
title_short Sitosterolemia: a review and update of pathophysiology, clinical spectrum, diagnosis, and management
title_sort sitosterolemia a review and update of pathophysiology clinical spectrum diagnosis and management
topic Sitosterolemia
Phytosterolemia
Hypercholesterolemia
Plant sterol
url http://e-apem.org/upload/pdf/apem-21-7.pdf
work_keys_str_mv AT eungyongyoo sitosterolemiaareviewandupdateofpathophysiologyclinicalspectrumdiagnosisandmanagement