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Glutamine Synthetase in Cerebrospinal Fluid, Serum, and Brain
A Diagnostic Marker for Alzheimer Disease?
Hayrettin Tumani, MD;
GuoQiu Shen, MD;
James B. Peter, MD, PhD;
Wolfgang Brück, MD
Arch Neurol. 1999;56:1241-1246.
Objectives To determine whether the glutamine synthetase (GS) level in cerebrospinal fluid (CSF) is a useful biochemical marker in the diagnosis of Alzheimer disease (AD), and to assess the source of GS (brain vs blood derived) in CSF.
Methods Sandwich enzyme immunoassay and immunoblotting were applied to detect GS in CSF and in serum from neurologically healthy control subjects and patients with neurodegenerative diseases, including AD. The origin of GS was estimated by the concentration gradients of CSF to serum and ventricular to lumbar CSF. In addition, postmortem brain tissue from controls and patients with AD was analyzed using immunohistochemistry for expression of GS.
Results Levels of GS were significantly increased in lumbar CSF from patients with AD (20±12 pg/mL; P=.01) and to a lesser extent in patients with vascular dementia and amyotrophic lateral sclerosis. In CSF of controls, GS levels were 4±3 pg/mL. The GS concentration gradients were less than 1:10 for CSF to serum and 2:1 for ventricular to lumbar CSF. Immunoreactivity of GS was most prominent in astrocytes from temporal neocortex of patients with AD, suggesting a relationship between astrocyte reactions and increased GS levels in CSF.
Conclusions Level of GS in lumbar CSF of patients with AD is increased significantly but nonspecifically, probably related to the strong astrogliosis in brain. Glutamine synthetase in lumbar CSF is mainly brain derived.
From the Department of Neurology (Dr Tumani) and the Institute of Neuropathology (Dr Brück), University of Göttingen, Göttingen, Germany; and Specialty Laboratories, Inc, Santa Monica, Calif (Drs Shen and Peter).
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