TY - JOUR
T1 - Correlation of lymphocyte heat shock protein 70 levels with neurologic deficits in elderly patients with cerebral infarction
AU - Jin, Xingfang
AU - Xiao, Chengfeng
AU - Tanguay, Robert M.
AU - Yang, Li
AU - Wang, Feng
AU - Chen, Ming
AU - Fu, Xiaoye
AU - Wang, Ru
AU - Deng, Jie
AU - Deng, Zhijun
AU - Zheng, Yongyong
AU - Wei, Qingyi
AU - Wu, Tangchun
N1 - Funding Information:
This work was supported in part by research funds from the National Key Basic Research and Development Program (2002CB512905) and from the National Natural Science Foundation of China (30128021 and 30371204) to Dr. Wu. Drs. Wu and Tanguay received financial support from the National Natural Science Foundation of China and the Canadian Institute of Health Research of Canada (CIHR) for a research exchange program and an operating CIHR grant.
PY - 2004/9/15
Y1 - 2004/9/15
N2 - To assess the association between heat shock protein 70 (HSP70) levels and the severity of ischemic stroke in elderly patients. We conducted a case-control study to investigate the changes in lymphocyte HSP70 levels by immunoblot in 65 elderly patients with mild (n = 22), intermediate (n = 21), or severe (n = 22) stroke, and in 34 healthy controls. We analyzed correlations between HSP70 levels and neurologic deficit scores on days 1, 15, and 30 after the onset of stroke. Mean (± SD) HSP70 levels were higher in all stroke patients compared with controls (mild stroke: 709 ± 194 units; intermediate: 585 ± 165 units; severe: 421 ± 124 units; controls: 86 ± 34 units on day 1). Patients with mild stroke had higher levels at day 1 and 15 than did patients with severe stroke. HSP70 levels decreased rapidly from days 1 to 30 in all patients, except in patients with severe stroke, in whom levels decreased slowly between days 15 and 30. There were significant negative correlations between HSP70 levels and neurologic deficit scores in patients on days 1 (r = -0.53, P <0.001) and 15 (r = -0.54, P <0.001), but a positive correlation on day 30 (r = 0.49, P <0.001). These data suggest that HSP70 may be a marker for neuroprotection in the early stage of ischemic stroke and a marker for a crisis in the later stages of severe cerebral infarction. Further studies on the use of lymphocyte HSP70 levels in predicting clinical outcomes and underlying mechanisms in cerebral infarction are warranted.
AB - To assess the association between heat shock protein 70 (HSP70) levels and the severity of ischemic stroke in elderly patients. We conducted a case-control study to investigate the changes in lymphocyte HSP70 levels by immunoblot in 65 elderly patients with mild (n = 22), intermediate (n = 21), or severe (n = 22) stroke, and in 34 healthy controls. We analyzed correlations between HSP70 levels and neurologic deficit scores on days 1, 15, and 30 after the onset of stroke. Mean (± SD) HSP70 levels were higher in all stroke patients compared with controls (mild stroke: 709 ± 194 units; intermediate: 585 ± 165 units; severe: 421 ± 124 units; controls: 86 ± 34 units on day 1). Patients with mild stroke had higher levels at day 1 and 15 than did patients with severe stroke. HSP70 levels decreased rapidly from days 1 to 30 in all patients, except in patients with severe stroke, in whom levels decreased slowly between days 15 and 30. There were significant negative correlations between HSP70 levels and neurologic deficit scores in patients on days 1 (r = -0.53, P <0.001) and 15 (r = -0.54, P <0.001), but a positive correlation on day 30 (r = 0.49, P <0.001). These data suggest that HSP70 may be a marker for neuroprotection in the early stage of ischemic stroke and a marker for a crisis in the later stages of severe cerebral infarction. Further studies on the use of lymphocyte HSP70 levels in predicting clinical outcomes and underlying mechanisms in cerebral infarction are warranted.
UR - https://www.scopus.com/pages/publications/5444265022
UR - https://www.scopus.com/pages/publications/5444265022#tab=citedBy
U2 - 10.1016/j.amjmed.2004.03.026
DO - 10.1016/j.amjmed.2004.03.026
M3 - Article
C2 - 15380497
AN - SCOPUS:5444265022
SN - 0002-9343
VL - 117
SP - 406
EP - 411
JO - American Journal of Medicine
JF - American Journal of Medicine
IS - 6
ER -