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. 1981 Jul;33(4):592-605.

Prevention of homozygous beta-thalassemia by carrier screening and prenatal diagnosis in Sardinia

A Cao, M Furbetta, R Galanello, M A Melis, A Angius, A Ximenes, C Rosatelli, R Ruggeri, M Addis, T Tuveri, A M Falchi, E Paglietti, M T Scalas

Prevention of homozygous beta-thalassemia by carrier screening and prenatal diagnosis in Sardinia

A Cao et al. Am J Hum Genet. 1981 Jul.

Abstract

We report here results of a 3-year pilot voluntary screening program coupled with prenatal diagnosis directed to the prospective prevention of homozygous beta-thalassemia (beta-thal) in Sardinia. The screening program took two approaches: outreach community testing and hospital testing on request after a period of sensibilization. The outreach testing was very effective as, taking into account the already known number of couples at risk with an affected proband (20), 74% of the couple at risk expected (61) on the basis of the carrier rate were identified. Less effective was the hospital testing in which half of the couples at risk expected were detected (502 with the 199 without an affected proband). After nondirective genetic counseling, approximately 85% of the couples at risk, which had a pregnancy, with no statistically significant difference between those with and those without a proband, requested prenatal testing. This figure showed a steadily increase from the beginning in 1977 to 1980. All the pregnancies (42), but two carrying homozygous fetuses, were terminated on parental request. A continuous hospital survey of thal-major admissions in the different hospitals of the counties showed a steady decline in the incidence figure at birth from 1976 (1:213) to 1978 (1:290). These results showed that even in a medium-developed, rural, Catholic population screening coupled with prenatal diagnosis can be successful in the control of a fatal, recessively inherited disorder.

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