4.5 Article

Pyroptosis executive protein GSDMD as a biomarker for diagnosis and identification of Alzheimer's disease

Journal

BRAIN AND BEHAVIOR
Volume 11, Issue 4, Pages -

Publisher

WILEY
DOI: 10.1002/brb3.2063

Keywords

Alzheimer' s disease; diagnosis; GSDMD; identification; pyroptosis

Funding

  1. Zhejiang Provincial Science and Technology Foundation [LGF19H090012]
  2. Jingly Science and Technology Foundation [2019AY32011]

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The levels of GSDMD, T-Tau, and Tau181p were higher in AD patients compared to VD patients and healthy controls, while A beta(1-42) levels were lower in AD patients. GSDMD showed good diagnostic accuracy in AD and good discrimination accuracy between AD and VD. The expression levels of inflammatory factors (IL-1 beta and IL-6) in the cerebrospinal fluid were higher in AD patients and positively correlated with GSDMD expression.
Objective This study was mainly conducted to explore the expression changes of GSDMD and conventional markers (including T-Tau, Tau181p, and A beta(1-42)) in the cerebrospinal fluid among patients with Alzheimer's disease (AD) and vascular dementia (VD), followed by determination of role of GSDMD in diagnosing and identifying AD and VD. Methods In this study, 60 patients with VD, 60 patients with AD, and 50 healthy controls were enrolled. Lumbar puncture was performed to collect cerebrospinal fluid samples. Patients with VD and patients with AD were evaluated using the Mini-Mental State Examination (MMSE) scale, Montreal Cognitive Assessment (MoCA) scale, Clinical Dementia Rating (CDR) scale, Activity of Daily Living (ADL) scale, and Neuropsychiatric Inventory (NPI) questionnaire, aiming to determine the behavioral ability of patients. ELISA kit was purchased to determine the levels of GSDMD, T-Tau, Tau181p, and A beta(1-42) in cerebrospinal fluid, and the expression of inflammatory factors, IL-1 beta and IL-6, was also detected. Results (1) The levels of GSDMD, T-Tau, and Tau181p in the cerebrospinal fluid were higher in patients with AD than those of patients with VD and healthy controls, while the levels of A beta(1-42) in the cerebrospinal fluid were lower in patients with AD than that in healthy controls and patients with VD. (2) GSDMD had good diagnostic accuracy in AD. Additionally, GSDMD, T-Tau, Tau181p, and A beta(1-42) had good discrimination accuracy in distinguishing AD and VD. (3) The expression levels of inflammatory factors (IL-1 beta and IL-6) in cerebrospinal fluid were higher in patients with AD than those of healthy controls and patients with VD, which were positively correlated with GSDMD expression. Conclusion The expression of GSDMD was increased in patients with AD, which could be used as a biomarker for AD diagnosis and identification from VD.

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