Evidence map›Paper›PMID 39041277›Full record

ArticleCurrent Alzheimer research2024

Associations of Multimorbidity with Cerebrospinal Fluid Biomarkers for Neurodegenerative Disorders in Early Parkinson's Disease: A Crosssectional and Longitudinal Study.

Ming-Zhan Zhang, Yan Sun, Yan-Ming Chen, Fan Guo, Pei-Yang Gao, Lan Tan, Meng-Shan Tan

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Article in Current Alzheimer research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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7 authors.

Ming-Zhan ZhangSchool of Clinical Medicine, Shandong Second Medical University (formerly Weifang Medical University), Weifang 261000, Shandong, China.
Yan SunDepartment of Neurology, Qingdao Municipal Hospital, Qingdao University, Qingdao, China.
Yan-Ming ChenDepartment of Neurology, Qingdao Municipal Hospital, Qingdao University, Qingdao, China.
Fan GuoDepartment of Neurology, Qingdao Municipal Hospital, Qingdao University, Qingdao, China.
Pei-Yang GaoDepartment of Neurology, Qingdao Municipal Hospital, Qingdao University, Qingdao, China.
Lan TanDepartment of Neurology, Qingdao Municipal Hospital, University of Health and Rehabilitation Sciences, Qingdao, China.
Meng-Shan TanSchool of Clinical Medicine, Shandong Second Medical University (formerly Weifang Medical University), Weifang 261000, Shandong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectThe study aims to determine whether multimorbidity status is associated with cerebrospinal fluid (CSF) biomarkers for neurodegenerative disorders.

methodsA total of 827 patients were enrolled from the Parkinson's Progression Markers Initiative (PPMI) database, including 638 patients with early-stage Parkinson's disease (PD) and 189 healthy controls (HCs). Multimorbidity status was evaluated based on the count of long-term conditions (LTCs) and the multimorbidity pattern. Using linear regression models, cross-sectional and longitudinal analyses were conducted to assess the associations of multimorbidity status with CSF biomarkers for neurodegenerative disorders, including α-synuclein (αSyn), amyloid-β

resultsAt baseline, the CSF t-tau (p = 0.010), p-tau (p = 0.034), and NfL (p = 0.049) levels showed significant differences across the three categories of LTC counts. In the longitudinal analysis, the presence of LTCs was associated with lower Aβ

conclusionMultimorbidity, especially severe multimorbidity and the pattern of mental/musculoskeletal/ tumor disorders, was associated with CSF biomarkers for neurodegenerative disorders in early-stage PD patients, suggesting that multimorbidity might play a crucial role in aggravating neuronal damage in neurodegenerative diseases.

Indexed as

Amyloid beta-PeptidesBiomarkersMultimorbidityParkinson Diseasetau ProteinsAgedalpha-SynucleinCross-Sectional StudiesFemaleHumansLongitudinal StudiesMaleMiddle AgedNeurodegenerative DiseasesNeurofilament ProteinsPeptide Fragmentsalpha-SynucleinAmyloid beta-Peptidesamyloid beta-protein (1-42)BiomarkersNeurofilament ProteinsPeptide Fragmentstau ProteinsAmyloid-β42cerebrospinal fluidglial fibrillary acidic proteinMultimorbidityneurofilament light chain protein.phosphorylated tautotal tauα- synuclein

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.