缺血性脑卒中患者血糖控制改善不能改变因子VIII水平。

Scientific times journal of diabetes Pub Date : 2017-06-01 Epub Date: 2017-03-20
Alyana A Samai, Amelia K Boehme, Alexander George, Laurie Schluter, Ramy El Khoury, Sheryl Martin-Schild
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引用次数: 0

摘要

目的:探讨急性缺血性脑卒中(AIS)患者血糖控制程度与因子VIII (FVIII)水平变化是否相关。方法:所有在2008年7月至2014年5月期间入院的基线HbA1c和FVIII水平的AIS患者均入选。其中包括出院后随访HbA1c和FVIII水平的患者。FVIII升高定义为水平>150%。根据HbA1c水平分为不控制(>7.1%)、控制(5.7-7.0%)和正常(结果:1631例AIS患者中,63例患者符合纳入标准。其中21例(33.3%)糖尿病未控制,27例(42.8%)糖尿病控制,15例(23.4%)血糖正常。基线人口统计学特征仅在高脂血症史上有差异(57.1%未控制,25.9%控制,26.7%正常,p=0.0443)。两组间FVIII和HbA1c的基线和随访时间无差异(p=0.0812和p=0.6969)。基线时HbA1C组与FVIII水平无相关性(p=0.2197),基线至随访期间HbA1C变化与FVIII变化无相关性(r=0.0147, p=0.9092)。此外,在基线或随访时无统计学显著水平。结论:虽然AIS急性期高血糖与FVIII水平相关,但AIS前后的长期血糖控制与FVIII水平无关。我们的研究结果表明,这些卒中危险因素是相互独立的,FVIII水平不能通过控制糖尿病来改变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Factor VIII Level is Not Modifiable by Improved Glycemic Control in Patients with Ischemic Stroke.

Aims: To determine whether the degree of glycemic control was related to change in Factor VIII (FVIII) level in patients with acute ischemic stroke (AIS).

Methods: From our stroke registry, all AIS patients admitted between 07/2008-05/2014 with baseline HbA1c and FVIII levels were eligible. Of these, patients with follow-up HbA1c and FVIII levels post-discharge were included. Elevation in FVIII was defined as level >150%. Diabetic control was categorized according to HbA1c levels:uncontrolled (>7.1%), controlled (5.7-7.0%), and normal (<5.7%) HbA1c and FVIII levels were further analyzed for evidence of a correlation as continuous variables.

Results: Among 1,631 AIS cases, 63 patients met inclusion criteria. Of these, 21 patients (33.3%) had uncontrolled diabetes, 27 patients (42.8%) had controlled diabetes, and 15 patients (23.4%) had normoglycemia. Baseline demographic characteristics differed only for history of hyperlipidemia (57.1% uncontrolled, 25.9% controlled, 26.7% normal, p=0.0443). Time between baseline and follow-up measures of both FVIII and HbA1c did not differ between groups (p=0.0812 and p=0.6969, respectively). There was no association between HbA1C group and FVIII level at baseline (p=0.2197) nor between change in HbA1c and change in FVIII from baseline to follow-up (r=0.0147, p=0.9092). Additionally, no statistically significant level at baseline or follow-up.

Conclusions: While hyperglycemia and FVIII level are associated in the acute phase of AIS, long-term glycemic control before or subsequent to AIS was unrelated to FVIII level. Our results suggest that these stroke risk factors are independent of each other and that FVIII level cannot be modified by controlling diabetes.

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