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Measurement of sCD27 in the cerebrospinal fluid identifies patients with neuroinflammatory disease.
Feresiadou, Amalia; Nilsson, Kenneth; Ingelsson, Martin; Press, Rayomand; Kmezic, Ivan; Nygren, Ingela; Svenningsson, Anders; Niemelä, Valter; Gordh, Torsten; Cunningham, Janet; Kultima, Kim; Larsson, Anders; Burman, Joachim.
Affiliation
  • Feresiadou A; Department of Neuroscience, Neurology, Uppsala University, Uppsala, Sweden.
  • Nilsson K; Department of Medical Sciences, Clinical Microbiology, Uppsala University, Uppsala, Sweden.
  • Ingelsson M; Department of Public Health and Caring Sciences, Section of Geriatrics, Uppsala University, Sweden.
  • Press R; Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.
  • Kmezic I; Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.
  • Nygren I; Department of Neuroscience, Neurology, Uppsala University, Uppsala, Sweden.
  • Svenningsson A; Department of Clinical Sciences, Karolinska Institutet, Danderyd Hospital, Stockholm, Sweden.
  • Niemelä V; Department of Neuroscience, Neurology, Uppsala University, Uppsala, Sweden.
  • Gordh T; Department of Surgical Sciences, Anesthesiology and Intensive Care, Uppsala University, Uppsala, Sweden.
  • Cunningham J; Department of of Neuroscience, Psychiatry, Uppsala University, Uppsala, Sweden.
  • Kultima K; Department of Medical Sciences, Clinical Chemistry, Uppsala University, Uppsala, Sweden.
  • Larsson A; Department of Medical Sciences, Clinical Chemistry, Uppsala University, Uppsala, Sweden.
  • Burman J; Department of Neuroscience, Neurology, Uppsala University, Uppsala, Sweden. Electronic address: joachim.burman@neuro.uu.se.
J Neuroimmunol ; 332: 31-36, 2019 07 15.
Article in En | MEDLINE | ID: mdl-30928869
BACKGROUND: Laboratory tests to assist in the diagnosis and monitoring of neuroinflammatory diseases are scarce. The soluble form of the CD27 molecule (sCD27) is shed in high concentrations by activated T cells and can be detected in the cerebrospinal fluid. The aim of this study was to investigate whether CSF quantitation of sCD27 could discriminate between inflammatory and non-inflammatory neurological diseases. METHODS: The concentration of sCD27 was measured using a commercially available ELISA in 803 well-defined subjects from a study cohort comprised of 338 patients with neuroinflammatory disease, 338 with non-inflammatory neurological disease and 127 controls without neurological disease. RESULTS: The median value of cerebrospinal fluid sCD27 was 64 pg/mL (IQR 0-200) in controls, 58 pg/mL (IQR 0-130) in patients with non-inflammatory disease and 740 pg/mL (IQR 230-1800) in patients with inflammatory disease. The likelihood ratio of having an inflammatory disease was 10 (sensitivity 74% and specificity 93%) if the sCD27 concentration was >250 pg/mL. In patients with a known inflammatory condition, the likelihood ratio of having an infection was 10 (sensitivity 40% and specificity 96%) if the sCD27 concentration was >2500 pg/mL. CONCLUSIONS: The likelihood of having an inflammatory neurological condition is increased with elevated concentrations of sCD27 in cerebrospinal fluid. Rapid tests of sCD27 should be developed to assist clinicians in diagnosis of neuroinflammatory disease.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cerebrospinal Fluid Proteins / Tumor Necrosis Factor Receptor Superfamily, Member 7 / Inflammation / Nervous System Diseases Type of study: Diagnostic_studies / Prognostic_studies Aspects: Patient_preference Limits: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: J Neuroimmunol Year: 2019 Document type: Article Affiliation country: Sweden Country of publication: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cerebrospinal Fluid Proteins / Tumor Necrosis Factor Receptor Superfamily, Member 7 / Inflammation / Nervous System Diseases Type of study: Diagnostic_studies / Prognostic_studies Aspects: Patient_preference Limits: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: J Neuroimmunol Year: 2019 Document type: Article Affiliation country: Sweden Country of publication: Netherlands