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Characterization of Severity in Zellweger Spectrum Disorder by Clinical Findings: A Scoping Review, Meta-Analysis and Medical Chart Review

Journal

CELLS
Volume 11, Issue 12, Pages -

Publisher

MDPI
DOI: 10.3390/cells11121891

Keywords

Zellweger spectrum disorder; peroxisome biogenesis disorder; signs and symptoms; PEX genes; disease severity; scoping review; medical chart review; seizure disorder; feeding difficulties; renal cysts; survival; hexacosanoic acid

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Funding

  1. Travere Therapeutics Inc.
  2. Global Foundation for Peroxisomal Disorders

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Zellweger spectrum disorder (ZSD) is a rare genetic disorder that affects multiple organ systems and has broad clinical heterogeneity. This study aimed to determine if the characterization of clinical findings can predict severity in ZSD. The results showed significant differences in certain clinical findings across severity categories, including seizures, hypotonia, reduced mobility, feeding difficulties, renal cysts, adrenal insufficiency, hearing and vision loss, and shortened lifespan. The findings provide important information for determining appropriate outcomes in clinical trials for ZSD.
Zellweger spectrum disorder (ZSD) is a rare, debilitating genetic disorder of peroxisome biogenesis that affects multiple organ systems and presents with broad clinical heterogeneity. Although severe, intermediate, and mild forms of ZSD have been described, these designations are often arbitrary, presenting difficulty in understanding individual prognosis and treatment effectiveness. The purpose of this study is to conduct a scoping review and meta-analysis of existing literature and a medical chart review to determine if characterization of clinical findings can predict severity in ZSD. Our PubMed search for articles describing severity, clinical findings, and survival in ZSD resulted in 107 studies (representing 307 patients) that were included in the review and meta-analysis. We also collected and analyzed these same parameters from medical records of 136 ZSD individuals from our natural history study. Common clinical findings that were significantly different across severity categories included seizures, hypotonia, reduced mobility, feeding difficulties, renal cysts, adrenal insufficiency, hearing and vision loss, and a shortened lifespan. Our primary data analysis also revealed significant differences across severity categories in failure to thrive, gastroesophageal reflux, bone fractures, global developmental delay, verbal communication difficulties, and cardiac abnormalities. Univariable multinomial logistic modeling analysis of clinical findings and very long chain fatty acid (VLCFA) hexacosanoic acid (C26:0) levels showed that the number of clinical findings present among seizures, abnormal EEG, renal cysts, and cardiac abnormalities, as well as plasma C26:0 fatty acid levels could differentiate severity categories. We report the largest characterization of clinical findings in relation to overall disease severity in ZSD. This information will be useful in determining appropriate outcomes for specific subjects in clinical trials for ZSD.

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