Reviews

Clinical Spectrum of Stiff Person Syndrome: A Review of Recent Reports

Authors:

Abstract

Background: ‘‘Classic’’ stiff person syndrome (SPS) features stiffness, anti-glutamic acid decarboxylase (anti-GAD) antibodies, and other findings. Anti-GAD antibodies are also detected in some neurological syndromes (such as ataxia) in which stiffness is inconsistently present. Patients with otherwise ‘‘classic’’ SPS may either lack anti-GAD antibodies or be seropositive for others. Hence, SPS cases appear to fall within a clinical spectrum that includes conditions such as progressive encephalomyelitis with rigidity and myoclonus (PERM), which exhibits brainstem and autonomic features. We have compiled herein SPS-spectrum cases reported since 2010, and have segregated them on the basis of likely disease mechanism (autoimmune, paraneoplastic, or cryptogenic) for analysis.

Methods: The phrases ‘‘stiff person syndrome’’, ‘‘PERM’’, ‘‘anti-GAD antibody syndrome’’, and ‘‘glycine receptor antibody neurological disorders’’ were searched for in PubMed in January 2015. The results were narrowed to 72 citations after excluding non-English and duplicate reports. Clinical descriptions, laboratory data, management, and outcomes were categorized, tabulated, and analyzed.

Results: Sixty-nine autoimmune, 19 paraneoplastic, and 13 cryptogenic SPS-spectrum cases were identified. SPS was the predominant diagnosis among the groups. Roughly two-thirds of autoimmune and paraneoplastic cases were female. Anti-GAD antibodies were most frequently identified, followed by antiamphiphysin among paraneoplastic cases and by anti-glycine receptor antibodies among autoimmune cases. Benzodiazepines were the most commonly used medications. Prognosis seemed best for cryptogenic cases; malignancy worsened that of paraneoplastic cases.

Discussion: Grouping SPS-spectrum cases by pathophysiology provided insights into work-up, treatment, and prognosis. Ample phenotypic and serologic variations are present within the categories. Ruling out malignancy and autoimmunity is appropriate for suspected SPS-spectrum cases.

Keywords:

Stiff person syndromestiff limb syndromestiff trunk syndromeprogressive encephalomyelitis with rigidity and myoclonusanti-glutamic acid decarboxylase antibodiesanti-glycine receptor antibodies
  • Year: 2016
  • Volume: 6
  • Page/Article: 340
  • DOI: 10.5334/tohm.316
  • Submitted on 25 Jul 2015
  • Accepted on 22 Dec 2015
  • Published on 4 Mar 2016
  • Peer Reviewed