The mucopolysaccharidoses are lysosomal disorders that progressively affect most organ systems in the body usually beginning in childhood. Recent treatment advances have produced some amelioration, but notably brain and bone have been difficult to treat. The long-term objectives of this research are to identify abnormalities of central nervous system (CNS) structure and function over time using quantitative neuropsychological, behavioral, and MRI techniques;to identify, those measures that are most sensitive to change;and to identify the impact of biological, environmental, and disease factors on outcomes. Findings in the current research have suggested 1) white matter is abnormal in both structure and function;2) significant psychosocial problems as MPS children age;and 3) need for better measurements.
Our specific aims are 1) to study corpus callosum and white matter volumes, diffusion tensor imaging (DTI) and a new MRI technique, resting state fMRI, by disease subtype over time compared to normal controls and in relationship to neuropsychological functions such as attention. 2) We will examine the impact of biological, environmental, and disease related factors on emotional and social function. 3) We will develop more precise outcome measures. In particular, we will develop an MPS-specific and sensitive quality-of-life measure that will measure both physical and psychosocial difficulties. Measurement of gait, physical symptom severity, pain, and disability will also be considered in relationship to emotional/social function and quality-of-life. Methods: We will accomplish this with 120+ patients, recruited in the past 4 years from 6 centers (70 MPS I, 30 MPS II, and 20 MPS VI). Each patient will be seen for a total of 3 or 4 follow-up visits with quantitative neuroimaging (volumetrics/DTI for all;fMRI for older patients) and neuropsychological tests (IQ, attention, memory, visual spatial) as well as adaptive behavior, quality-of-life and emotion including behavior, temperament, and self-esteem. Data will be analyzed for 1) age changes in white matter and psychological adjustment, 2) the sensitivity of measures to disease progression, and 3) variables that contribute to outcomes. These results will enable prevention and interventions to enhance long-term functional outcomes.

Public Health Relevance

Neurobehavioral function and quality-of-life are compromised in many patients with MPS disorders. This research can 1) more accurately inform patients/parents regarding potential neurobehavioral outcomes, 2) develop sensitive measures of disease progression and CNS treatment outcome, and 3) help clinical researchers develop direct treatments to specific brain structures/functions.

National Institute of Health (NIH)
National Institute of Neurological Disorders and Stroke (NINDS)
Specialized Center--Cooperative Agreements (U54)
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Special Emphasis Panel (ZTR1-CI-8 (01))
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Morris, Jill A
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University of Minnesota Twin Cities
United States
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Schneider, Joseph; Burmeister, Lynn A; Rudser, Kyle et al. (2016) Hypothyroidism in late-onset Pompe disease. Mol Genet Metab Rep 8:24-7
Polgreen, Lynda E; Vehe, Richard K; Rudser, Kyle et al. (2016) Elevated TNF-α is associated with pain and physical disability in mucopolysaccharidosis types I, II, and VI. Mol Genet Metab 117:427-30
Shapiro, Elsa G; Rudser, Kyle; Ahmed, Alia et al. (2016) A longitudinal study of emotional adjustment, quality of life and adaptive function in attenuated MPS II. Mol Genet Metab Rep 7:32-9
Dyke, J P; Sondhi, D; Voss, H U et al. (2016) Brain Region-Specific Degeneration with Disease Progression in Late Infantile Neuronal Ceroid Lipofuscinosis (CLN2 Disease). AJNR Am J Neuroradiol 37:1160-9
Najafian, Behzad; Tøndel, Camilla; Svarstad, Einar et al. (2016) One Year of Enzyme Replacement Therapy Reduces Globotriaosylceramide Inclusions in Podocytes in Male Adult Patients with Fabry Disease. PLoS One 11:e0152812
Shapiro, E; King, K; Ahmed, A et al. (2016) The Neurobehavioral Phenotype in Mucopolysaccharidosis Type IIIB: an Exploratory Study. Mol Genet Metab Rep 6:41-47
Rappaport, Jeff; Manthe, Rachel L; Solomon, Melani et al. (2016) A Comparative Study on the Alterations of Endocytic Pathways in Multiple Lysosomal Storage Disorders. Mol Pharm 13:357-68
Ahmed, Alia; Shapiro, Elsa; Rudser, Kyle et al. (2016) Association of somatic burden of disease with age and neuropsychological measures in attenuated mucopolysaccharidosis types I, II and VI. Mol Genet Metab Rep 7:27-31
Karimian, Zahra; Whitley, Chester B; Rudser, Kyle D et al. (2016) Delayed Infusion Reactions to Enzyme Replacement Therapies. JIMD Rep :
Kazi, Zoheb B; Prater, Sean N; Kobori, Joyce A et al. (2016) Durable and sustained immune tolerance to ERT in Pompe disease with entrenched immune responses. JCI Insight 1:

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