Literature DB >> 20715120

Prevalence of steroid sulfatase deficiency in California according to race and ethnicity.

Wendy Y Craig1, Marie Roberson, Glenn E Palomaki, Cedric H L Shackleton, Josep Marcos, James E Haddow.   

Abstract

OBJECTIVE: Estimate steroid sulfatase deficiency (STSD) prevalence among California's racial/ethnic groups using data from a previous study focused on prenatal detection of Smith-Lemli-Opitz syndrome (SLOS). SLOS and STSD both have low maternal serum unconjugated estriol (uE3) levels.
METHODS: Prevalence was estimated using three steps: listing clinically identified cases; modeling STSD frequency at three uE3 intervals using diagnostic urine steroid measurements; applying this model to determine frequency in pregnancies not providing urine.
RESULTS: Overall, 2151 of 777 088 pregnancies (0.28%) were screen positive; 1379 of these were explained and excluded. Fifty-four cases were diagnosed clinically among 707 remaining pregnancies with a male fetus. Urine steroid testing identified 74 additional STSD cases: 66 (89.2%) at uE3 values < 0.15 MoM, 8 (10.8%) at 0.15-0.20 MoM, and 0 (0%) at > 0.20 MoM. Modeling estimated 107.5 STSD cases among 370 pregnancies without urine samples. In males, STSD prevalence was highest among non-Hispanic Whites (1:1230) compared to Hispanics (1:1620) and Asians (1:1790), but differences were not significant. No STSD pregnancies were found among 65 screen positive Black women.
CONCLUSION: The overall prevalence estimate of 1:1500 males is consistent with published estimates and is reasonable for counseling, except among Black pregnancies where no reliable estimate could be made. (c) 2010 John Wiley & Sons, Ltd.

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Year:  2010        PMID: 20715120     DOI: 10.1002/pd.2588

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  13 in total

1.  Pre-Descemet corneal dystrophy and X-linked ichthyosis associated with deletion of Xp22.31 containing the STS gene.

Authors:  Crystal Hung; Reed I Ayabe; Cynthia Wang; Ricardo F Frausto; Anthony J Aldave
Journal:  Cornea       Date:  2013-09       Impact factor: 2.651

2.  An IL-17-dominant immune profile is shared across the major orphan forms of ichthyosis.

Authors:  Amy S Paller; Yael Renert-Yuval; Maria Suprun; Hitokazu Esaki; Margeaux Oliva; Thy Nhat Huynh; Benjamin Ungar; Norma Kunjravia; Rivka Friedland; Xiangyu Peng; Xiuzhong Zheng; Yeriel D Estrada; James G Krueger; Keith A Choate; Mayte Suárez-Fariñas; Emma Guttman-Yassky
Journal:  J Allergy Clin Immunol       Date:  2016-08-20       Impact factor: 10.793

Review 3.  Adrenal disorders in pregnancy.

Authors:  Silvia Monticone; Richard J Auchus; William E Rainey
Journal:  Nat Rev Endocrinol       Date:  2012-09-11       Impact factor: 43.330

4.  Estrogen Promotes Microvascularization in the Fetus and Thus Vascular Function and Insulin Sensitivity in Offspring.

Authors:  Eugene D Albrecht; Graham W Aberdeen; Jeffery S Babischkin; Steven J Prior; Terrie J Lynch; Irene A Baranyk; Gerald J Pepe
Journal:  Endocrinology       Date:  2022-05-01       Impact factor: 5.051

5.  Behavioural and Psychiatric Phenotypes in Men and Boys with X-Linked Ichthyosis: Evidence from a Worldwide Online Survey.

Authors:  Sohini Chatterjee; Trevor Humby; William Davies
Journal:  PLoS One       Date:  2016-10-06       Impact factor: 3.240

6.  Behavioural and psychiatric phenotypes in female carriers of genetic mutations associated with X-linked ichthyosis.

Authors:  Alice Cavenagh; Sohini Chatterjee; William Davies
Journal:  PLoS One       Date:  2019-02-15       Impact factor: 3.240

Review 7.  The Regulation of Steroid Action by Sulfation and Desulfation.

Authors:  Jonathan W Mueller; Lorna C Gilligan; Jan Idkowiak; Wiebke Arlt; Paul A Foster
Journal:  Endocr Rev       Date:  2015-07-27       Impact factor: 19.871

8.  Steroid Sulfatase Deficiency and Androgen Activation Before and After Puberty.

Authors:  Jan Idkowiak; Angela E Taylor; Sandra Subtil; Donna M O'Neil; Raymon Vijzelaar; Renuka P Dias; Rakesh Amin; Timothy G Barrett; Cedric H L Shackleton; Jeremy M W Kirk; Celia Moss; Wiebke Arlt
Journal:  J Clin Endocrinol Metab       Date:  2016-03-22       Impact factor: 5.958

9.  X-linked ichthyosis: Molecular findings in four pedigrees with inconspicuous clinical manifestations.

Authors:  Min Zhang; Hailong Huang; Na Lin; Shuqiong He; Gang An; Yan Wang; Meihuan Chen; Lingji Chen; Yuan Lin; Liangpu Xu
Journal:  J Clin Lab Anal       Date:  2020-01-16       Impact factor: 2.352

10.  Medical and neurobehavioural phenotypes in carriers of X-linked ichthyosis-associated genetic deletions in the UK Biobank.

Authors:  Lucija Brcic; Jack Fg Underwood; Kimberley M Kendall; Xavier Caseras; George Kirov; William Davies
Journal:  J Med Genet       Date:  2020-03-05       Impact factor: 6.318

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