Health-related quality of life in mucopolysaccharidosis: looking beyond biomedical issues. Issue 1 (December 2016)

• Record Type: Journal Article
• Authors: Hendriksz, Christian; Berger, Kenneth; Lampe, Christina; Kircher, Susanne; Orchard, Paul; Southall, Rebecca; Long, Sarah; Sande, Stephen; Gold, Jeffrey
• Is Part Of: Orphanet journal of rare diseases. Volume 11:Issue 1(2016)
• Page Start: 1
• Page End: 15
• Publication Date: 2016-12
• Subjects: Mucopolysaccharidoses -- Quality of life -- Enzyme replacement therapy -- Clinical trial -- Pain measurement -- EQ-5D -- MPS HAQ -- HRQoL -- ADL; Rare diseases -- Periodicals; Genetic disorders -- Periodicals; Orphan drugs -- Periodicals; 616
• DOI: 10.1186/s13023-016-0503-2
• Languages: English
• ISSNs: 1750-1172

Abstract

Abstract The mucopolysaccharidoses (MPS) comprise a heterogeneous family of rare, genetic lysosomal storage disorders that result in severe morbidity and reduced life expectancy. Emerging treatments for several of these disorders have triggered the search for clinically relevant biomarkers and clinical markers associated with treatment efficacy in populations and individuals. However, biomedical measures do not tell the whole story when characterizing a complex chronic disorder such as MPS. Health-related quality of life (HRQoL) tools that utilize patient reported outcomes to address patient parameters such as symptoms (pain, fatigue, psychological health), functioning (activity and limitations), or quality of life, have been used to supplement traditional biomedical endpoints. Many of these HRQoL tools have demonstrated that quality of life is negatively impacted in patients with MPS. There is both the opportunity and need to formally standardize and validate HRQoL tools for the different MPS disorders.