| Literature DB >> 25502769 |
Alberto Sánchez-Guijo1, Vinzenz Oji2, Michaela F Hartmann1, Hans-Christian Schuppe3, Heiko Traupe2, Stefan A Wudy1.
Abstract
Steroid sulfatase (STS) deficiency is the underlying cause of the skin condition known as recessive X-linked ichthyosis (RXLI). RXLI patients show scales on their skin caused by high concentrations of cholesterol sulfate (CS), as they are not capable of releasing the sulfate group from its structure to obtain free cholesterol. CS has been reported, so far, as the sole sulfated steroid with increased concentrations in the blood of RXLI patients. A non-targeted LC-MS approach in negative mode detection (LC-MS precursor ion scan mode) was applied to serum samples of 12 RXLI patients and 19 healthy males. We found that CS was not the only sulfated compound consistently elevated in RXLI patients, because a group of compounds with a m/z of 481 was found in high concentrations too. Further LC-MS/MS demonstrated that the main contributor to the m/z 481 signal in RXLI serum is 27-hydroxycholesterol-3-sulfate (27OHC3S). Accordingly, a new method for 27OHC3S quantification in the context of RXLI has been developed and validated. Other hydroxycholesterol sulfate compounds were elevated as well in RXLI patients.Entities:
Keywords: liquid chromatography/mass spectrometry; recessive X-linked ichthyosis; steroid metabolism; sulfated steroids
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Year: 2014 PMID: 25502769 PMCID: PMC4306693 DOI: 10.1194/jlr.M055608
Source DB: PubMed Journal: J Lipid Res ISSN: 0022-2275 Impact factor: 5.922