Literature DB >> 6940862

Increased cholesterol sulfate in plasma and red blood cell membranes of steroid sulfatase deficient patients.

E A Bergner, L J Shapiro.   

Abstract

Steroid sulfatase deficiency is an inborn error of metabolism characterized during fetal life by decreased estriol production and postnatally by x-=linked ichthyosis. No consistent substrate abnormalities have been found beyond the perinatal period. Utilizing gas chromatography, we found that the cholesterol sulfate concentration was less than 350 micrograms/100 ml plasma in 9 normal adults, 2 subjects with ichthyosis vulgaris and 2 subjects with lamellar ichthyosis. Control red cell membranes had less than 300 micrograms/100 ml erythrocytes. Eight subjects (age 3 months-74 years) with steroid sulfatase deficiency had strikingly elevated cholesterol sulfate levels with means and ranges as follows: plasma - 3,300 micrograms/100 ml (2,700-4,000), red cell membranes- 7,500 (5,200-9,800) Cholesterol sulfate is known to effect membrane stability and the present observations may help to explain the pathogenesis of STS deficiency and x-linked ichthyosis.

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Year:  1981        PMID: 6940862     DOI: 10.1210/jcem-53-1-220

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  16 in total

Review 1.  Review: placental sulphatase deficiency.

Authors:  N F Taylor
Journal:  J Inherit Metab Dis       Date:  1982       Impact factor: 4.982

2.  Simplified determination of serum cholesterol sulfate by gas-liquid chromatography combined with cyclohexylsilane-bonded phase column purification.

Authors:  S Serizawa; T Nagai; M Ito; Y Sato
Journal:  Arch Dermatol Res       Date:  1989       Impact factor: 3.017

3.  High levels of oxysterol sulfates in serum of patients with steroid sulfatase deficiency.

Authors:  Alberto Sánchez-Guijo; Vinzenz Oji; Michaela F Hartmann; Hans-Christian Schuppe; Heiko Traupe; Stefan A Wudy
Journal:  J Lipid Res       Date:  2014-12-11       Impact factor: 5.922

4.  Cholesterol sulphate in the microsomal sulphatase deficient placenta.

Authors:  A Marinkovic-Ilsen; M L Williams
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

5.  Higher levels of plasma cholesterol sulfate in patients with liver cirrhosis and hypercholesterolemia.

Authors:  N Tamasawa; A Tamasawa; K Takebe
Journal:  Lipids       Date:  1993-09       Impact factor: 1.880

6.  Recessive X-linked ichthyosis: lack of immunologically detectable steroid sulfatase enzyme protein.

Authors:  E H Epstein; J M Bonifas
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

7.  Excretion of (sulfated) steroids in the urine and excretion of cholesterol sulfate in the feces of boys with recessive X-linked ichthyosis.

Authors:  A Marinkovic-Ilsen; A van den Ende; B G Wolthers
Journal:  Arch Dermatol Res       Date:  1984       Impact factor: 3.017

8.  Cloning of a cDNA for steroid sulfatase: frequent occurrence of gene deletions in patients with recessive X chromosome-linked ichthyosis.

Authors:  J M Bonifas; B J Morley; R E Oakey; Y W Kan; E H Epstein
Journal:  Proc Natl Acad Sci U S A       Date:  1987-12       Impact factor: 11.205

9.  Stratum corneum lipids in disorders of cornification. Steroid sulfatase and cholesterol sulfate in normal desquamation and the pathogenesis of recessive X-linked ichthyosis.

Authors:  P M Elias; M L Williams; M E Maloney; J A Bonifas; B E Brown; S Grayson; E H Epstein
Journal:  J Clin Invest       Date:  1984-10       Impact factor: 14.808

10.  Mutations in SULT2B1 Cause Autosomal-Recessive Congenital Ichthyosis in Humans.

Authors:  Lisa Heinz; Gwang-Jin Kim; Slaheddine Marrakchi; Julie Christiansen; Hamida Turki; Marc-Alexander Rauschendorf; Mark Lathrop; Ingrid Hausser; Andreas D Zimmer; Judith Fischer
Journal:  Am J Hum Genet       Date:  2017-06-01       Impact factor: 11.025

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