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Primary Sjögren's syndrome is associated with significant cognitive dysfunction
Mehmet Engin Tezcan1, Emine Belgin Kocer2, Seminur Haznedaroglu3
1Department of Rheumatology, Lutfi Kirdar Kartal Education and Training Hospital, Ankara, Turkey. engintez@yahoo.com.
Cognitive dysfunction is common in primary Sjögren syndrome (PSS). Neurologic tests revealed deficits in attention and memory in PSS patients, but these were not linked to specific antibodies.
Area of Science:
- Neurology
- Immunology
- Rheumatology
Background:
- Primary Sjögren syndrome (PSS) is an autoimmune disorder that can manifest with neurological symptoms, including cognitive dysfunction.
- Specific antibodies have been implicated in cognitive impairment, necessitating further investigation in PSS patients.
Purpose of the Study:
- To comprehensively assess cognitive dysfunction in patients with PSS using detailed neurologic tests.
- To investigate the association between cognitive deficits and the presence of specific antibodies in PSS.
Main Methods:
- A cohort of 28 female PSS patients and 17 healthy controls underwent extensive neurologic testing.
- Evaluated cognitive domains included memory, verbal learning, attention, executive functions, and processing speed.
- Assessed for anti-N-methyl-D-aspartate (NMDA) receptor antibody, anti-ribosomal-P, and antiganglioside antibodies.
Main Results:
- PSS patients demonstrated significantly lower performance in attention, processing speed, verbal learning, short-term verbal memory, and visuo-spatial perception compared to controls.
- Specific tests like the Paced Auditory Serial Addition Test and Serial Digit Learning Test showed statistically significant differences (P < 0.01).
- While antiganglioside antibodies were more frequent in PSS patients, their presence did not correlate with the observed cognitive dysfunction.
Conclusions:
- Cognitive dysfunction is highly prevalent in patients diagnosed with primary Sjögren syndrome.
- The cognitive impairments observed in PSS patients were not associated with the presence of the evaluated antibodies (anti-NMDA receptor, anti-ribosomal-P, antiganglioside).
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