A Monogenic Disease with a Variety of Phenotypes: Deficiency of Adenosine Deaminase 2

J Rheumatol. 2020 Jan;47(1):117-125. doi: 10.3899/jrheum.181384. Epub 2019 May 1.

Abstract

Objective: Deficiency of adenosine deaminase 2 (DADA2) is an autosomal recessive autoinflammatory disorder associated with ADA2 mutations. We aimed to investigate the characteristics and ADA2 enzyme activities of patients with DADA2 compared to non-DADA2 patients.

Methods: This is a descriptive study of 24 patients with DADA2 who were admitted to the Adult and Pediatric Rheumatology, Pediatric Haematology, and Pediatric Immunology Departments of Hacettepe University. All ADA2 exons were screened by Sanger sequencing. Serum ADA2 enzyme activity was measured by modified spectrophotometric method.

Results: Twenty-four patients with DADA2 were included: 14 with polyarteritis nodosa (PAN)-like phenotype (Group 1); 9 with Diamond-Blackfan anemia (DBA)-like features, and 1 with immunodeficiency (Group 2). Fourteen PAN-like DADA2 patients did not have the typical thrombocytosis seen in classic PAN. Inflammatory attacks were evident only in Group 1 patients. Serum ADA2 activity was low in all patients with DADA2 except one, who was tested after hematopoietic stem cell transplantation. There was no significant difference in ADA2 activities between PAN-like and DBA-like patients. In DADA2 patients with one ADA2 mutation, serum ADA2 activities were as low as those of patients with homozygote DADA2. ADA2 activities were normal in non-DADA2 patients. ADA2 mutations were affecting the dimerization domain in Group 1 patients and the catalytic domain in Group 2 patients.

Conclusion: We suggest assessing ADA2 activity along with genetic analysis because there are patients with one ADA2 mutation and absent enzyme activity. Our data suggest a possible genotype-phenotype correlation in which dimerization domain mutations are associated with PAN-like phenotype, and catalytic domain mutations are associated with hematological manifestations.

Keywords: ADENOSINE DEAMINASE 2 DEFICIENCY; DIAMOND-BLACKFAN ANEMIA; POLYARTERITIS NODOSA PURE RED CELL ANEMIA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Deaminase / blood
  • Adenosine Deaminase / chemistry
  • Adenosine Deaminase / deficiency*
  • Adenosine Deaminase / genetics*
  • Adolescent
  • Adult
  • Agammaglobulinemia / blood
  • Agammaglobulinemia / enzymology*
  • Anemia, Diamond-Blackfan / blood
  • Anemia, Diamond-Blackfan / enzymology*
  • Catalytic Domain / genetics
  • Child
  • Child, Preschool
  • Cohort Studies
  • Dimerization
  • Exons
  • Female
  • Genetic Association Studies
  • Genetic Predisposition to Disease
  • Hematopoietic Stem Cell Transplantation
  • Homozygote
  • Humans
  • Intercellular Signaling Peptides and Proteins / blood
  • Intercellular Signaling Peptides and Proteins / chemistry
  • Intercellular Signaling Peptides and Proteins / deficiency*
  • Intercellular Signaling Peptides and Proteins / genetics*
  • Male
  • Middle Aged
  • Mutation
  • Phenotype*
  • Polyarteritis Nodosa / blood
  • Polyarteritis Nodosa / enzymology*
  • Severe Combined Immunodeficiency / blood
  • Severe Combined Immunodeficiency / enzymology*
  • Young Adult

Substances

  • Intercellular Signaling Peptides and Proteins
  • ADA2 protein, human
  • Adenosine Deaminase

Supplementary concepts

  • Severe combined immunodeficiency due to adenosine deaminase deficiency