Neural Regeneration Research (Jan 2020)

Serum cystatin C levels are negatively correlated with post-stroke cognitive dysfunction

  • Dao-Xia Guo,
  • Zheng-Bao Zhu,
  • Chong-Ke Zhong,
  • Xiao-Qing Bu,
  • Li-Hua Chen,
  • Tan Xu,
  • Li-Bing Guo,
  • Jin-Tao Zhang,
  • Dong Li,
  • Jian-Hui Zhang,
  • Zhong Ju,
  • Chung-Shiuan Chen,
  • Jing Chen,
  • Yong-Hong Zhang,
  • Jiang He

DOI
https://doi.org/10.4103/1673-5374.268928
Journal volume & issue
Vol. 15, no. 5
pp. 922 – 928

Abstract

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Stroke is the leading cause of death and long-term disability worldwide, and cognitive impairment and dementia are major complications of ischemic stroke. Cystatin C (CysC) has been found to be a neuroprotective factor in animal studies. However, the relationship between CysC levels and cognitive dysfunction in previous studies has revealed different results. This prospective observational study investigated the correlation between serum CysC levels and post-stroke cognitive dysfunction at 3 months. Data from 638 patients were obtained from the China Antihypertensive Trial in Acute Ischemic Stroke (CATIS). Cognitive dysfunction was assessed using the Mini-Mental State Examination (MMSE) at 3 months after stroke. According to the MMSE score, 308 patients (52.9%) had post-stroke cognitive dysfunction. After adjusting for potential confounding factors, the odds ratio (95% CI) of post-stroke cognitive dysfunction for the highest quartile of serum CysC levels was 0.54 (0.30–0.98), compared with the lowest quartile. The correlation between serum CysC and cognitive dysfunction was modified by renal function status. We observed a negative linear dose-response correlation between CysC and cognitive dysfunction in patients with normal renal function (Plinearity = 0.044), but not in those with abnormal renal function. Elevated serum CysC levels were correlated with a low risk of 3-month cognitive dysfunction in patients with acute ischemic stroke, especially in those with normal renal function. The current results suggest that CysC is a protective factor for post-stroke cognitive dysfunction, and could be used to treat post-stroke cognitive dysfunction. The CATIS study was approved by the Institutional Review Boards at Soochow University from China (approval No. 2012-02) on December 30, 2012, and was registered at ClinicalTrials.gov (identifier No. NCT01840072) on April 25, 2013.

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