Neurological phenotype of adenosine deaminase 2 deficient patients: a cohort study

Author:

Verschoof Merelijne A.1ORCID,van Meenen Laura C. C.2ORCID,Andriessen M. Valérie E.3,Brinkman Daniëlle M. C.4,Kamphuis Sylvia5,Kuijpers Taco W.6,Leavis Helen L.7,Legger G. Elizabeth8,Mulders‐Manders Catharina M.9,de Pagter Anne P. J.4,Rutgers Abraham10,van Well Gijs T. J.11,Coutinho Jonathan M.2,Hak A. Elisabeth12,van Montfrans Joris M.3,Klouwer Femke C. C.213ORCID

Affiliation:

1. Department of Neurology HagaZiekenhuis The Hague The Netherlands

2. Department of Neurology Amsterdam UMC, University of Amsterdam Amsterdam The Netherlands

3. Department of Pediatric Immunology and Infectious Diseases University Medical Center Utrecht Utrecht The Netherlands

4. Department of Pediatrics Willem‐Alexander Children's Hospital, Leiden University Medical Center Leiden The Netherlands

5. Department of Pediatric Rheumatology Sophia Children's Hospital, Erasmus University Medical Center Rotterdam Rotterdam The Netherlands

6. Department of Pediatric Immunology and Infectious Diseases Amsterdam UMC, University of Amsterdam Amsterdam The Netherlands

7. Department of Rheumatology and Clinical Immunology University Medical Center and Utrecht University Utrecht The Netherlands

8. Department of Pediatric Rheumatology and Immunology University Groningen, University Medical Center Groningen Groningen The Netherlands

9. Department of Internal Medicine, Radboud Expertise Center for Immunodeficiency and Autoinflammation Radboud University Medical Center Nijmegen The Netherlands

10. Department of Rheumatology and Clinical Immunology University Groningen, University Medical Center Groningen Groningen The Netherlands

11. Division of Pediatric Infectious Diseases, Immunology & Rheumatology, Department of Pediatrics Maastricht University Medical Center Maastricht The Netherlands

12. Departments of Internal Medicine and Rheumatology and Clinical Immunology Amsterdam UMC, University of Amsterdam Amsterdam The Netherlands

13. Department of Pediatric Neurology Emma Children's Hospital, Amsterdam UMC, University of Amsterdam Amsterdam The Netherlands

Abstract

AbstractBackground and purposePatients with adenosine deaminase 2 (ADA2) deficiency can present with various neurological manifestations due to vasculopathies and autoinflammation. These include ischaemic and hemorrhagic stroke, but less clearly defined neurological symptoms have also been reported.MethodsIn this cohort study, patients with confirmed ADA2 deficiency from seven university hospitals in the Netherlands were included. The frequency and recurrence rates of neurological manifestations before and after initiation of tumor necrosis factor α (TNF‐α) inhibiting therapy were analyzed.ResultsTwenty‐nine patients were included with a median age at presentation of 5 years (interquartile range 1–17). Neurological manifestations occurred in 19/29 (66%) patients and were the presenting symptom in 9/29 (31%) patients. Transient ischaemic attack (TIA)/ischaemic stroke occurred in 12/29 (41%) patients and was the presenting symptom in 8/29 (28%) patients. In total, 25 TIAs/ischaemic strokes occurred in 12 patients, one after initiation of TNF‐α inhibiting therapy and one whilst switching between TNF‐α inhibitors. None was large‐vessel occlusion stroke. Two hemorrhagic strokes occurred: one aneurysmatic subarachnoid hemorrhage and one spontaneous intracerebral hemorrhage. Most neurological symptoms, including cranial nerve deficits, vertigo, ataxia and seizures, were caused by TIAs/ischaemic strokes and seldom recurred after initiation of TNF‐α inhibiting therapy.ConclusionsNeurological manifestations, especially TIA/ischaemic stroke, are common in patients with ADA2 deficiency and frequently are the presenting symptom. Because it is a treatable cause of young stroke, for which antiplatelet and anticoagulant therapy are considered contraindicated, awareness amongst neurologists and pediatricians is important. Screening for ADA2 deficiency in young patients with small‐vessel ischaemic stroke without an identified cause should be considered.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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