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21 years of Wiskott-Aldrich syndrome in Spain: incidence, mortality, and gender bias
A Guerrero Espejo1, S Tomás Dols1, M C Gestal2
1Grupo de Investigación de Enfermedades Infecciosas, Faculty of Medicine and Dentistry, Catholic University of Valencia "San Vicente Mártir", Valencia, Spain.
Background:
Wiskott-Aldrich syndrome (WAS) is a rare X-linked disorder considered to predominantly affect males.
Objective:
This study aims to investigate the incidence and intrahospital death associated with WAS in Spain as well as the gender bias.
Methods:
A population-based retrospective epidemiological study of 97 WAS patients that were diagnosed in Spanish hospitals between 1997 and 2017 was conducted by using data from the National Surveillance System for Hospital Data.
Results:
Our results revealed that the mean annual incidence of WAS in Spain was 1.1 per 10,000,000 inhabitants (IC95% 0,45-2,33). The relative risk was higher in male than female (2.42). WAS diagnosis occurs at later ages in women (median age of 47 years) compared to men (median age of 5.5 years). Only male were admitted to the hospital at least in 10 different occasions and all deaths were detected in men. The intra-hospital death rate was of 9.28% in WAS, being most of the deaths associated with brain hemorrhage or infection.
Conclusions:
WAS, a rare disease, is diagnoses at later ages in women and the mortality was found in males mostly associated with brain hemorrhage and infection.
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