机构:[1]Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China重点科室诊疗科室神经病学中心首都医科大学附属天坛医院[2]China National Clinical Research Center for Neurological Diseases, Beijing, China[3]Center of Stroke, Beijing Institute for Brain Disorders, Beijing, China[4]Beijing Key Laboratory of Translational Medicine for Cerebrovascular Disease, Beijing, China[5]Department of Epidemiology and Health Statistics, School of Public Health, Capital Medical University, Beijing, China[6]Beijing Municipal Key Laboratory of Clinical Epidemiology, Beijing, China.
Objectives: Hemoglobin A1c (HbA1c) has been recommended for diagnosing diabetes mellitus (DM). We aimed to assess the prevalence of newly diagnosed diabetes mellitus (NDDM) in patients with intracerebral hemorrhage (ICH) using HbA1c criteria and to investigate the long-term prognosis of patients with ICH with NDDM. Materials and Methods: Data of patients with ICH without a DM history were derived from the Abnormal Glucose Regulation in Patients with Acute Stroke across China. NDDM was defined as a fasting plasma glucose (FPG) level of 7.0 mmol/L or higher, a 2-hour oral glucose tolerance test (OGTT) result of 11.1 mmol/L or higher, or an HbA1c level of 6.5% or higher. The prevalence of NDDM with different screening methods was assessed. The association between NDDM and 1-year prognosis (mortality, stroke recurrence, and poor functional outcome [modified Rankin scale score of 3-6]) was estimated. Results: There were 357 patients with ICH included in the analysis, and 131 (36.7%) were diagnosed as NDDM using the new criteria. NDDM was present in 31 (8.7%), 98 (27.5%), and 68 (19.0%) patients with ICH, based on FPG, 2-hour OGTT, and HbA1c criteria, respectively. NDDM was independently associated with 1-year poor functional outcome (odds ratio 1.93; 95% confidence interval, 1.10-3.38, P=.02). Nevertheless, NDDM showed no significant association with 1-year death and stroke recurrence (P>.05 for both). Conclusions: More than one third of patients with ICH without a history of DM were diagnosed NDDM using the new criteria. NDDM by the new criteria was an independent risk factor of poor functional outcome, but not of death and stroke recurrence at 1 year after ICH onset. (c) 2018 Published by Elsevier Inc. on behalf of National Stroke Association.
基金:
National Key Technology Research and Development Program of the Ministry of Science and Technology of the People's Republic of China [2015BAI12B04, 2015BAI12B02]; Beijing Municipal Administration of Hospitals' Mission Plan [SML20150502]
第一作者机构:[1]Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China[2]China National Clinical Research Center for Neurological Diseases, Beijing, China[3]Center of Stroke, Beijing Institute for Brain Disorders, Beijing, China[4]Beijing Key Laboratory of Translational Medicine for Cerebrovascular Disease, Beijing, China
通讯作者:
通讯机构:[1]Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China[2]China National Clinical Research Center for Neurological Diseases, Beijing, China[3]Center of Stroke, Beijing Institute for Brain Disorders, Beijing, China[4]Beijing Key Laboratory of Translational Medicine for Cerebrovascular Disease, Beijing, China[*1]No. 6 Tiantanxili, Dongcheng District, Beijing 100050, China.
推荐引用方式(GB/T 7714):
Xinmiao Zhang,Jing Jing,Huaguang Zheng,et al.Prognosis of Intracerebral Hemorrhage with Newly Diagnosed Diabetes Mellitus According to Hemoglobin A1c Criteria[J].JOURNAL OF STROKE & CEREBROVASCULAR DISEASES.2018,27(5):1127-1133.doi:10.1016/j.jstrokecerebrovasdis.2017.11.019.
APA:
Xinmiao Zhang,Jing Jing,Huaguang Zheng,Qian Jia,Xingquan Zhao...&Yongjun Wang.(2018).Prognosis of Intracerebral Hemorrhage with Newly Diagnosed Diabetes Mellitus According to Hemoglobin A1c Criteria.JOURNAL OF STROKE & CEREBROVASCULAR DISEASES,27,(5)
MLA:
Xinmiao Zhang,et al."Prognosis of Intracerebral Hemorrhage with Newly Diagnosed Diabetes Mellitus According to Hemoglobin A1c Criteria".JOURNAL OF STROKE & CEREBROVASCULAR DISEASES 27..5(2018):1127-1133