Translational Psychiatry (May 2022)

Associations of plasma angiostatin and amyloid-β and tau levels in Alzheimer’s disease

  • Yuan Cheng,
  • Jun-Rong Ren,
  • Jie-Ming Jian,
  • Chen-Yang He,
  • Man-Yu Xu,
  • Gui-Hua Zeng,
  • Cheng-Rong Tan,
  • Ying-Ying Shen,
  • Wang-Sheng Jin,
  • Dong-Wan Chen,
  • Hui-Yun Li,
  • Xu Yi,
  • Yuan Zhang,
  • Xian-Le Bu,
  • Yan-Jiang Wang

DOI
https://doi.org/10.1038/s41398-022-01962-6
Journal volume & issue
Vol. 12, no. 1
pp. 1 – 6

Abstract

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Abstract Angiostatin, an endogenous angiogenesis inhibitor generated by the proteolytic cleavage of plasminogen, was recently reported to contribute to the development of Alzheimer’s disease (AD). However, whether there are pathological changes in angiostatin levels in individuals with AD dementia is unclear, and whether plasma angiostatin has a relationship with major AD pathological processes and cognitive impairment remains unknown. To examine plasma angiostatin levels in patients with AD dementia and investigate the associations of angiostatin with blood and cerebrospinal fluid (CSF) AD biomarkers, we conducted a cross-sectional study including 35 cognitively normal control (CN) subjects and 59 PiB-PET-positive AD dementia patients. We found that plasma angiostatin levels were decreased in AD dementia patients compared to CN subjects. Plasma angiostatin levels were negatively correlated with plasma Aβ42 and Aβ40 levels in AD dementia patients and positively correlated with CSF total tau (t-tau) levels and t-tau/Aβ42 in AD dementia patients with APOE-ε4. In addition, plasma angiostatin levels had the potential to distinguish AD from CN. These findings suggest a link between angiostatin and AD pathogenesis and imply that angiostatin might be a potential diagnostic biomarker for AD.