Newborn tandem mass spectroscopy screening for adenosine deaminase deficiency

Ann Allergy Asthma Immunol. 2022 Dec;129(6):776-783.e2. doi: 10.1016/j.anai.2022.07.016. Epub 2022 Jul 30.

Abstract

Background: Newborn screening (NBS) by means of T cell receptor excision circles (TREC) is now universal in the United States, Puerto Rico, and the Navajo Nation as a strategy to identify severe combined immunodeficiency (SCID) in newborns. Owing to the characteristics of adenosine deaminase (ADA) deficiency, a small but important number of cases can be missed by this screening.

Objective: To evaluate the results of the first year statewide NBS for ADA by means of dried blood spot NBS.

Methods: On October 7, 2019, the state of Michigan began screening newborn dried blood spots for ADA deficiency by means of the Neobase-2 tandem mass spectroscopy (TMS) kit. We report 1 known case of ADA deficiency in the 18 months before screening. We then reviewed the results of the first 2 years of TMS ADA screening in Michigan.

Results: There was 1 patient with ADA deficiency known to our centers in the 18 months before initiation of TMS ADA screening; this patient died of complications of their disease. In the first 2 years of TMS ADA NBS, 206,321 infants were screened, and 2 patients had positive ADA screen results. Both patients had ADA deficiency confirmed through biochemical and genetic testing. One patient identified also had a positive TREC screen and was confirmed to have ADA-SCID.

Conclusion: In our first 2 years, TMS NBS for ADA deficiency identified 2 patients with ADA deficiency at negligible cost, including 1 patient who would not have been identified by TREC NBS. This report provides initial evidence of the value of specific NBS for ADA deficiency.

MeSH terms

  • Agammaglobulinemia* / diagnosis
  • Humans
  • Infant
  • Infant, Newborn
  • Mass Spectrometry
  • Neonatal Screening / methods
  • Severe Combined Immunodeficiency* / diagnosis
  • Severe Combined Immunodeficiency* / genetics

Supplementary concepts

  • Severe combined immunodeficiency due to adenosine deaminase deficiency