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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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 |
work_keys_str_mv |
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