Τίτλος:
Quantitative clinical and autoimmune assessments in stiff person syndrome: Evidence for a progressive disorder
Γλώσσες Τεκμηρίου:
Αγγλικά
Περίληψη:
Background: Stiff Person Syndrome (SPS) is an under-diagnosed disorder that affects mobility and the quality of life of affected patients. The aim of the study is to describe the natural history of SPS, the extent of accumulated disability and the associated clinical and immunological features in patients followed for up to 8 years in a single center. Methods: Our collective cohort included 57 SPS patients. Additionally, 32 of these patients were examined every 6 months for a two-year period in a longitudinal study protocol, to assess disease progression using quantitative measures of stiffness and heightened sensitivity. Results: The most frequent initial symptom was leg stiffness, followed by paraspinal muscle rigidity and painful spasms in 95% of the patients. Although none of the patients required assistance for ambulation during the first 2 years of disease onset, 46 patients (80%) lost the ability to walk independently during our follow-up, despite symptomatic medications. In the longitudinal cohort, the number of stiff areas increased (p < 0.0001), consistent with worsening functional status and quality of life. High-titer anti-GAD antibodies were present in serum and CSF with elevated intrathecal GAD-specific IgG synthesis, but they did not correlate with clinical severity or progression. Conclusions: This large study on SPS patients, combining an eight-year follow-up at a single center by the same leading neurologist and his team, is the first to provide longitudinal data in a large patient subgroup using objective clinical measures. One of the main findings is that SPS is a progressive disease leading to physical disability over time. © 2019 The Author(s).
Συγγραφείς:
Rakocevic, G.
Alexopoulos, H.
Dalakas, M.C.
Εκδότης:
BioMed Central Ltd.
Λέξεις-κλειδιά:
glutamate decarboxylase antibody; immunoglobulin G, adult; antibody blood level; antibody titer; Article; autoimmune disease; cohort analysis; controlled study; disease exacerbation; female; functional status; gene frequency; human; immunogenetics; immunoglobulin production; longitudinal study; major clinical study; male; muscle rigidity; muscle spasm; musculoskeletal stiffness; paraspinal muscle; physical disability; quality of life; stiff man syndrome; disease exacerbation, Cohort Studies; Disease Progression; Humans; Quality of Life; Stiff-Person Syndrome
DOI:
10.1186/s12883-018-1232-z
