Female Patients With Mucopolysaccharidosis <scp>II</scp> ( <scp>MPS II</scp> ): Insights From the Hunter Outcome Survey

Mucopolysaccharidosis II is a rare, X-linked disease, with very few reports of affected female patients. Natural history data describe a predominantly male population, and appropriate disease characterization in female patients is lacking. This analysis explores the somatic disease burden and clinical progression of female patients with MPS II enrolled in the Hunter Outcome Survey (HOS; NCT03292887), a global disease registry. In total, 15 female patients were identified, representing 1.1% of the total patients in HOS. The median ages at first symptom onset and diagnosis were 1.8 and 3.1 years, respectively. A total of 8/14 (57.1%) of patients had cognitive impairment at the latest visit. X-chromosome abnormalities were reported in two patients. Most patients (11/15, 73.3%) had received at least one dose of idursulfase, which was generally well tolerated; no serious adverse events during follow-up were considered treatment-related. Musculoskeletal and ear symptoms were present in all 14 patients with data recorded. Almost all females also experienced neurological, abdominal/gastrointestinal, and pulmonary disease, similar to the symptomatology reported in males. Most patients underwent surgery (41 procedures in 12 patients). Two participants had a male sibling with MPS II who was also enrolled in HOS. Both sibling sets had missense variants and demonstrated several differences in signs/symptoms between the male and female siblings. Notably, only the female siblings displayed cognitive impairment. This report illustrates the disease burden in female patients with MPS II, helping to inform clinicians about the likely prognosis for this extremely rare subgroup of patients.

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Publication Details

Journal
JIMD Reports
Published
2025-12-02
DOI
https://doi.org/10.1002/jmd2.70046
Primary Topic
Lysosomal Storage Disorders Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Female Patients With Mucopolysaccharidosis II ( MPS II ): Insights From the Hunter Outcome Survey

Maurizio Scarpa, Jennifer Audi, Siddarth Jain, Anna Tylki‐Szymańska et al.
JIMD Reports
Lysosomal Storage Disorders Research
article

Female Patients With Mucopolysaccharidosis II ( MPS II ): Insights From the Hunter Outcome Survey

Maurizio Scarpa, Jennifer Audi, Siddarth Jain, Anna Tylki‐Szymańska, Jaco Botha, Christoph Kampmann, Joseph Muenzer, Roberto Giugliani, Barbara K. Burton, Hernán Amartino, Julian Raiman
article en

Abstract

Mucopolysaccharidosis II is a rare, X-linked disease, with very few reports of affected female patients. Natural history data describe a predominantly male population, and appropriate disease characterization in female patients is lacking. This analysis explores the somatic disease burden and clinical progression of female patients with MPS II enrolled in the Hunter Outcome Survey (HOS; NCT03292887), a global disease registry. In total, 15 female patients were identified, representing 1.1% of the total patients in HOS. The median ages at first symptom onset and diagnosis were 1.8 and 3.1 years, respectively. A total of 8/14 (57.1%) of patients had cognitive impairment at the latest visit. X-chromosome abnormalities were reported in two patients. Most patients (11/15, 73.3%) had received at least one dose of idursulfase, which was generally well tolerated; no serious adverse events during follow-up were considered treatment-related. Musculoskeletal and ear symptoms were present in all 14 patients with data recorded. Almost all females also experienced neurological, abdominal/gastrointestinal, and pulmonary disease, similar to the symptomatology reported in males. Most patients underwent surgery (41 procedures in 12 patients). Two participants had a male sibling with MPS II who was also enrolled in HOS. Both sibling sets had missense variants and demonstrated several differences in signs/symptoms between the male and female siblings. Notably, only the female siblings displayed cognitive impairment. This report illustrates the disease burden in female patients with MPS II, helping to inform clinicians about the likely prognosis for this extremely rare subgroup of patients.

JIMD ReportsVol. 67(1)
Northwestern University (US), University of North Carolina at Chapel Hill (US), University of Udine (IT), Lurie Children's Hospital (US), Universidade Federal do Rio Grande do Sul (BR), Johannes Gutenberg University Mainz (DE), Takeda (Switzerland) (CH), University Medical Center of the Johannes Gutenberg University Mainz (DE), Hospital Universitario Austral (AR), Children's Memorial Health Institute (PL), National Institute on Population Medical Genetics (BR), Takeda (United States) (US), Birmingham Women’s and Children’s NHS Foundation Trust (GB), Centro de Genomas (Brazil) (BR)
Takeda Pharmaceuticals International
Openalex Percentile: Top 53%
Lysosomal Storage Disorders Research
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