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Elevated cholesterol precursors other than cholestanol can also be a hallmark for CTX
Author(s) -
Sainvan der Velden M. G. M.,
Verrips A.,
Prinsen B. H. C. M. T.,
Barse M.,
Berger R.,
Visser G.
Publication year - 2008
Publication title -
journal of inherited metabolic disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.462
H-Index - 102
eISSN - 1573-2665
pISSN - 0141-8955
DOI - 10.1007/s10545-008-0963-1
Subject(s) - cholestanol , lathosterol , desmosterol , cholesterol , medicine , campesterol , endocrinology , cerebrotendinous xanthomatosis , sterol , lanosterol , chenodeoxycholic acid , chemistry , biology
Summary Cerebrotendinous xanthomatosis (CTX) is an inborn error of bile acid synthesis in which hepatic conversion of cholesterol to cholic and chenodeoxycholic acids is impaired. Patients have abnormal bile alcohols in urine, normal to increased plasma cholesterol concentrations and increased concentrations of plasma cholestanol. Little is known about cholesterol precursors in CTX, however. We studied cholesterol and phytosterol profiles in two siblings with CTX during follow‐up. While cholesterol concentrations were low in both patients, plasma cholestanol was 6‐fold higher compared to control values. In addition, both siblings had a more than 100‐fold increase in 7‐dehydrocholesterol (7DHC) and 8‐dehydrocholesterol (8DHC). Lathosterol, lanosterol and sitosterol were increased in both patients while concentrations of desmosterol and campesterol were normal. In addition, plasma lathosterol/cholesterol ratios were significantly elevated. After treatment with chenodeoxycholate, both patients showed a marked decrease in cholestanol, 7DHC, 8DHC, lathosterol, lanosterol and sitosterol. In addition, the lathosterol/cholesterol ratio normalized, indicating that overall cholesterol synthesis was sufficiently suppressed. This study shows that elevated cholesterol precursors, other than cholestanol, can be a hallmark for CTX.