Abstract

BackgroundCongenital adrenal hyperplasia (CAH) cause life-threatening adrenal crisis. It also affects fetal sex development and can result in incorrect sex assignment at birth. In 1989, a newborn screening program for congenital adrenal hyperplasia (CAH) was introduced in Tokyo. Here we present the results of this screening program in order to clarify the efficiency of CAH screening and the incidence of CAH in Japan.MethodFrom 1989 to 2013, a total of 2,105,108 infants were screened for CAH. The cutoff level for diagnosis of CAH was adjusted for gestational age and birth weight.ResultsA total of 410 infants were judged positive, and of these, 106 patients were diagnosed with CAH, indicating a positive predictive value (PPV) of 25.8 %. Of the 106 patients, 94 (88.7 %) were diagnosed with 21-OHD. Of these 94 patients, 73 were diagnosed with the salt wasting form, 14 with the simple virilising form and 7 with the nonclassical form (NC21OHD). The mean birth weight and gestational age were 3192 ± 385 g and 38.9 ± 1.38 weeks. 11 out of 44 female patients were assigned as female according to their screening result.ConclusionsThese data suggest that the newborn screening in Tokyo was effective, especially for sex assignment and preventing fatal adrenal crisis. The incidence of CAH was similar to that measured in previous Japanese screening studies, and it was also similar to that of western countries. The incidence of NC21OHD in Japan in the present study was lower than that in western countries as previous studies reported. The screening program achieved higher PPV than previous CAH screening studies, which might be due to the use of variable cutoffs according to gestational age and birth weight. However, most of the neonates born at 37 weeks or less that were referred to hospital were false-positives. Further changes are needed to reduce the number of false positive preterm neonates.

Highlights

  • Congenital adrenal hyperplasia (CAH) cause life-threatening adrenal crisis

  • A total of 410 infants were judged positive, and of these, 106 patients were diagnosed with CAH, indicating a positive predictive value (PPV) of 25.8 %

  • These data suggest that the newborn screening in Tokyo was effective, especially for sex assignment and preventing fatal adrenal crisis

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Summary

Introduction

Congenital adrenal hyperplasia (CAH) cause life-threatening adrenal crisis. It affects fetal sex development and can result in incorrect sex assignment at birth. In 1989, a newborn screening program for congenital adrenal hyperplasia (CAH) was introduced in Tokyo. More than 90 % of cases result from 21-hydroxylase deficiency (21-OHD) caused by mutations in CYP21A2 [1, 2]. Virilisation of external genitalia in newborn females and precocious puberty due to overproduction of androgens from the adrenal cortex are major clinical problems of both the SW and SV forms. In the SW form, in addition to overproduction of androgens, Tsuji et al BMC Pediatrics (2015) 15:209 aldosterone is deficient and it causes life-threatening adrenal crisis

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