Amyloid related cerebral microbleed and plasma Aβ40 are associated with cognitive decline in Parkinson's disease.

作者: Chin-Hsien Lin , Li-Kai Tsai , Hsin-Hsi Tsai , Yen-Ling Lo

DOI: 10.1038/S41598-021-86617-0

关键词: GastroenterologyBiomarker (medicine)NeurologyLogistic regressionConfoundingParkinson's diseaseMedicineDementiaInternal medicineConfidence intervalCognitive decline

摘要: Cerebral microbleeds (MBs) have been found in patients with cognitive decline. We aimed to examine whether MBs are associated motor or decline Parkinson’s disease (PD). enrolled 135 PD and 34 healthy controls. All participants underwent brain MRI plasma biomarker assays, including tau, Aβ42, Aβ40, α-synuclein. dementia (PDD) was operationally defined as Mini-Mental State Examination (MMSE) score < 26 advanced stage Hoehn-Yahr stage ≥ 3 during “on” status. The association between severity examined using multivariate logistic regression models. More lobar were observed than controls (20.7% vs. 3.3%, p = 0.031). PDD had more (33.3% 15.6%, p = 0.034), white matter hyperintensity (p = 0.021) reduced hippocampal volume (p = 0.001) normal cognition. presence of MB (odds ratio = 2.83 [95% confidence interval 1.04–7.70], p = 0.042) severe (3.29 [1.21–8.96], p = 0.020) independently after adjusting for vascular risk factors other confounders. Furthermore, Aβ40 levels the MMSE score (p = 0.004) age sex. Our findings demonstrated that MBs, volume, elevated PDD.

参考文章(46)
Marshal F. Folstein, Susan E. Folstein, Paul R. McHugh, “Mini-mental state” Journal of Psychiatric Research. ,vol. 12, pp. 189- 198 ,(1975) , 10.1016/0022-3956(75)90026-6
Philip Scheltens, Timo Erkinjunti, Didier Leys, Lars-Olaf Wahlund, Domenico Inzitari, Theodoro del Ser, Florence Pasquier, Frederik Barkhof, Riita Mäntylä, John Bowler, Anders Wallin, Joseph Ghika, Franz Fazekas, Leonardo Pantoni, White Matter Changes on CT and MRI: An Overview of Visual Rating Scales European Neurology. ,vol. 39, pp. 80- 89 ,(1998) , 10.1159/000007921
D. Aarsland, K. Andersen, J.P. Larsen, A. Lolk, H. Nielsen, P. Kragh-Sorensen, Risk of dementia in Parkinson’s disease: A community-based, prospective study Neurology. ,vol. 56, pp. 730- 736 ,(2001) , 10.1212/WNL.56.6.730
Kiyoshi Niwa, George A. Carlson, Costantino Iadecola, Exogenous Aβ1–40 Reproduces Cerebrovascular Alterations Resulting from Amyloid Precursor Protein Overexpression in Mice Journal of Cerebral Blood Flow and Metabolism. ,vol. 20, pp. 1659- 1668 ,(2000) , 10.1097/00004647-200012000-00005
M. E. Gurol, M. C. Irizarry, E. E. Smith, S. Raju, R. Diaz-Arrastia, T. Bottiglieri, J. Rosand, J. H. Growdon, S. M. Greenberg, Plasma β-amyloid and white matter lesions in AD, MCI, and cerebral amyloid angiopathy Neurology. ,vol. 66, pp. 23- 29 ,(2006) , 10.1212/01.WNL.0000191403.95453.6A
Ki Woong Kim, James R. MacFall, Martha E. Payne, Classification of White Matter Lesions on Magnetic Resonance Imaging in Elderly Persons Biological Psychiatry. ,vol. 64, pp. 273- 280 ,(2008) , 10.1016/J.BIOPSYCH.2008.03.024
A J Hughes, S E Daniel, L Kilford, A J Lees, Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases. Journal of Neurology, Neurosurgery, and Psychiatry. ,vol. 55, pp. 181- 184 ,(1992) , 10.1136/JNNP.55.3.181
S. Hoops, S. Nazem, A. D. Siderowf, J. E. Duda, S. X. Xie, M. B. Stern, D. Weintraub, Validity of the MoCA and MMSE in the detection of MCI and dementia in Parkinson disease Neurology. ,vol. 73, pp. 1738- 1745 ,(2009) , 10.1212/WNL.0B013E3181C34B47
Kurt A. Jellinger, Johannes Attems, Prevalence and impact of vascular and Alzheimer pathologies in Lewy body disease Acta Neuropathologica. ,vol. 115, pp. 427- 436 ,(2008) , 10.1007/S00401-008-0347-5
K. A. Jellinger, K. Seppi, G. K. Wenning, W. Poewe, Impact of coexistent Alzheimer pathology on the natural history of Parkinson's disease. Journal of Neural Transmission. ,vol. 109, pp. 329- 339 ,(2002) , 10.1007/S007020200027