The frequency of Tay-Sachs disease causing mutations in the Brazilian Jewish population justifies a carrier screening program

CONTEXT: Tay-Sachs disease is an autosomal recessive disease characterized by progressive neurologic degeneration, fatal in early childhood. In the Ashkenazi Jewish population the disease incidence is about 1 in every 3,500 newborns and the carrier frequency is 1 in every 29 individuals. Carrier scr...

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Main Authors: Roberto Rozenberg, Lygia da Veiga Pereira
Format: Article
Language:English
Published: Associação Paulista de Medicina
Series:São Paulo Medical Journal
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-31802001000400007&lng=en&tlng=en
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spelling doaj-6d0edb2cde004a83a838a71a1821096e2020-11-24T22:02:16ZengAssociação Paulista de MedicinaSão Paulo Medical Journal1806-9460119414614910.1590/S1516-31802001000400007S1516-31802001000400007The frequency of Tay-Sachs disease causing mutations in the Brazilian Jewish population justifies a carrier screening programRoberto Rozenberg0Lygia da Veiga Pereira1Universidade de São PauloUniversidade de São PauloCONTEXT: Tay-Sachs disease is an autosomal recessive disease characterized by progressive neurologic degeneration, fatal in early childhood. In the Ashkenazi Jewish population the disease incidence is about 1 in every 3,500 newborns and the carrier frequency is 1 in every 29 individuals. Carrier screening programs for Tay-Sachs disease have reduced disease incidence by 90% in high-risk populations in several countries. The Brazilian Jewish population is estimated at 90,000 individuals. Currently, there is no screening program for Tay-Sachs disease in this population. OBJECTIVE: To evaluate the importance of a Tay-Sachs disease carrier screening program in the Brazilian Jewish population by determining the frequency of heterozygotes and the acceptance of the program by the community. SETTING: Laboratory of Molecular Genetics - Institute of Biosciences - Universidade de São Paulo. PARTICIPANTS: 581 senior students from selected Jewish high schools. PROCEDURE: Molecular analysis of Tay-Sachs disease causing mutations by PCR amplification of genomic DNA, followed by restriction enzyme digestion. RESULTS: Among 581 students that attended educational classes, 404 (70%) elected to be tested for Tay-Sachs disease mutations. Of these, approximately 65% were of Ashkenazi Jewish origin. Eight carriers were detected corresponding to a carrier frequency of 1 in every 33 individuals in the Ashkenazi Jewish fraction of the sample. CONCLUSION: The frequency of Tay-Sachs disease carriers among the Ashkenazi Jewish population of Brazil is similar to that of other countries where carrier screening programs have led to a significant decrease in disease incidence. Therefore, it is justifiable to implement a Tay-Sachs disease carrier screening program for the Brazilian Jewish population.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-31802001000400007&lng=en&tlng=enTay-Sachs diseaseGenetic screeningHEXA geneJewish populationMolecular diagnosis
collection DOAJ
language English
format Article
sources DOAJ
author Roberto Rozenberg
Lygia da Veiga Pereira
spellingShingle Roberto Rozenberg
Lygia da Veiga Pereira
The frequency of Tay-Sachs disease causing mutations in the Brazilian Jewish population justifies a carrier screening program
São Paulo Medical Journal
Tay-Sachs disease
Genetic screening
HEXA gene
Jewish population
Molecular diagnosis
author_facet Roberto Rozenberg
Lygia da Veiga Pereira
author_sort Roberto Rozenberg
title The frequency of Tay-Sachs disease causing mutations in the Brazilian Jewish population justifies a carrier screening program
title_short The frequency of Tay-Sachs disease causing mutations in the Brazilian Jewish population justifies a carrier screening program
title_full The frequency of Tay-Sachs disease causing mutations in the Brazilian Jewish population justifies a carrier screening program
title_fullStr The frequency of Tay-Sachs disease causing mutations in the Brazilian Jewish population justifies a carrier screening program
title_full_unstemmed The frequency of Tay-Sachs disease causing mutations in the Brazilian Jewish population justifies a carrier screening program
title_sort frequency of tay-sachs disease causing mutations in the brazilian jewish population justifies a carrier screening program
publisher Associação Paulista de Medicina
series São Paulo Medical Journal
issn 1806-9460
description CONTEXT: Tay-Sachs disease is an autosomal recessive disease characterized by progressive neurologic degeneration, fatal in early childhood. In the Ashkenazi Jewish population the disease incidence is about 1 in every 3,500 newborns and the carrier frequency is 1 in every 29 individuals. Carrier screening programs for Tay-Sachs disease have reduced disease incidence by 90% in high-risk populations in several countries. The Brazilian Jewish population is estimated at 90,000 individuals. Currently, there is no screening program for Tay-Sachs disease in this population. OBJECTIVE: To evaluate the importance of a Tay-Sachs disease carrier screening program in the Brazilian Jewish population by determining the frequency of heterozygotes and the acceptance of the program by the community. SETTING: Laboratory of Molecular Genetics - Institute of Biosciences - Universidade de São Paulo. PARTICIPANTS: 581 senior students from selected Jewish high schools. PROCEDURE: Molecular analysis of Tay-Sachs disease causing mutations by PCR amplification of genomic DNA, followed by restriction enzyme digestion. RESULTS: Among 581 students that attended educational classes, 404 (70%) elected to be tested for Tay-Sachs disease mutations. Of these, approximately 65% were of Ashkenazi Jewish origin. Eight carriers were detected corresponding to a carrier frequency of 1 in every 33 individuals in the Ashkenazi Jewish fraction of the sample. CONCLUSION: The frequency of Tay-Sachs disease carriers among the Ashkenazi Jewish population of Brazil is similar to that of other countries where carrier screening programs have led to a significant decrease in disease incidence. Therefore, it is justifiable to implement a Tay-Sachs disease carrier screening program for the Brazilian Jewish population.
topic Tay-Sachs disease
Genetic screening
HEXA gene
Jewish population
Molecular diagnosis
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-31802001000400007&lng=en&tlng=en
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