Literature DB >> 23230938

Tay Sachs disease in Australia: reduced disease incidence despite stable carrier frequency in Australian Jews.

Raelia M Lew1, Anne L Proos, Leslie Burnett, Martin Delatycki, Agnes Bankier, Michael J Fietz.   

Abstract

OBJECTIVES: To evaluate the outcomes of preconception screening of Jewish Australians for Tay Sachs disease (TSD) carrier status on Jewish TSD-affected births. DESIGN, PARTICIPANTS AND
SETTING: Epidemiological observational study involving a complete retrospective audit of infantile and intermediate TSD cases diagnosed in Sydney and Melbourne between 1 January 1995 and 31 December 2011 (Royal Children's Hospital Melbourne; Pacific Laboratory Medicine Services, Pathology North, NSW Health Pathology, Sydney; Victorian Clinical Genetics Services, Melbourne; and SA Pathology, Adelaide), and carrier frequency among Jewish high school students attending schools participating in TSD screening programs over the same period. MAIN OUTCOME MEASURES: Jewish TSD carrier frequency; and expected versus observed Jewish TSD-affected births.
RESULTS: The 2006 Census indicated that most of the total 88,826 Jewish Australians live in Melbourne (46%) and Sydney (40%). The 7,756 Jewish high school students screened for TSD in Sydney and Melbourne during the study period had a carrier frequency of one in 31 (3.26%; 95% CI, 2.89%-3.68%).The estimated expected number of TSD-affected births in Melbourne and Sydney in 1995-2011 was 4.1 for Jewish births and 7.4 for other births (a ratio of Jewish to non-Jewish births of 1:2). The actual number was 12 (four in Sydney and eight in Melbourne), of which two were Jewish (a ratio of Jewish to non-Jewish births of 1:5). This finding of fewer than expected Jewish TSD cases coincided with a period during which screening programs were operating. There have been no Jewish TSD-affected children born to parents who were screened previously.
CONCLUSION: Community education, appreciation of autosomal recessive inheritance and genetic carrier screening before pregnancy are the likely factors in our finding of fewer than expected Jewish babies with TSD. Ongoing outcome monitoring must continue.

Entities:  

Mesh:

Year:  2012        PMID: 23230938     DOI: 10.5694/mja12.11010

Source DB:  PubMed          Journal:  Med J Aust        ISSN: 0025-729X            Impact factor:   7.738


  6 in total

1.  Community attitudes towards a Jewish community BRCA1/2 testing program.

Authors:  Nicole Cousens; Rajneesh Kaur; Bettina Meiser; Lesley Andrews
Journal:  Fam Cancer       Date:  2017-01       Impact factor: 2.375

Review 2.  Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents.

Authors:  Jeffrey R Botkin; John W Belmont; Jonathan S Berg; Benjamin E Berkman; Yvonne Bombard; Ingrid A Holm; Howard P Levy; Kelly E Ormond; Howard M Saal; Nancy B Spinner; Benjamin S Wilfond; Joseph D McInerney
Journal:  Am J Hum Genet       Date:  2015-07-02       Impact factor: 11.025

Review 3.  Tay-Sachs disease: current perspectives from Australia.

Authors:  Raelia M Lew; Leslie Burnett; Anné L Proos; Martin B Delatycki
Journal:  Appl Clin Genet       Date:  2015-01-21

4.  Therapeutic benefit after intracranial gene therapy delivered during the symptomatic stage in a feline model of Sandhoff disease.

Authors:  Victoria J McCurdy; Aime K Johnson; Heather L Gray-Edwards; Ashley N Randle; Allison M Bradbury; Nancy E Morrison; Misako Hwang; Henry J Baker; Nancy R Cox; Miguel Sena-Esteves; Douglas R Martin
Journal:  Gene Ther       Date:  2020-09-03       Impact factor: 5.250

5.  Evaluating the model of offering expanded genetic carrier screening to high school students within the Sydney Jewish community.

Authors:  Kristine Barlow-Stewart; Kayley Bardsley; Elle Elan; Jane Fleming; Yemima Berman; Ron Fleischer; Krista Recsei; Daniel Goldberg; John Tucker; Leslie Burnett
Journal:  J Community Genet       Date:  2021-11-30

Review 6.  Reproductive genetic carrier screening and inborn errors of metabolism: The voice of the inborn errors of metabolism community needs to be heard.

Authors:  Edwin P Kirk; Martin B Delatycki; Nigel Laing
Journal:  J Inherit Metab Dis       Date:  2022-05-09       Impact factor: 4.750

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.