Low Hemoglobin Causes Hematoma Expansion and Poor Intracerebral Hemorrhage Outcomes.

IF 8.9 1区 医学 Q1 CLINICAL NEUROLOGY Stroke Pub Date : 2025-05-01 Epub Date: 2025-03-20 DOI:10.1161/STROKEAHA.124.049499
Azzurra Cottarelli, Rayan Mamoon, Robin Ji, Eric Mao, Amelia Boehme, Aditya Kumar, Sandy Song, Valentina Allegra, Sabrina V Sharma, Elisa Konofagou, Vadim Spektor, Jia Guo, E Sander Connolly, Padmini Sekar, Daniel Woo, David J Roh
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Abstract

Background: Although lower hemoglobin levels associate with worse intracerebral hemorrhage (ICH) outcomes, causal drivers for this relationship remain unclear. We investigated the hypothesis that lower hemoglobin relates to increased hematoma expansion risk and poor outcomes using human observational data and assessed causal relationships using a translational murine model of anemia and ICH.

Methods: A multicenter, prospective observational cohort study of 2997 patients with ICH enrolled between 2010 and 2016 was assessed. Patients with baseline hemoglobin measurements and serial computed tomography neuroimaging were included for analyses. Patients with systemic evidence of coagulopathy were excluded. Separate regression models assessed relationships of baseline hemoglobin with hematoma expansion (≥33% and/or ≥6 mL growth) and poor long-term neurological outcomes (modified Rankin Scale score of 4-6) after adjusting for relevant covariates. Using a murine collagenase ICH model with serial neuroimaging in anemic versus nonanemic C57/BL6 mice, intergroup differences in ICH lesion volume, lesion volume changes, and early mortality were assessed.

Results: Among 1190 ICH patients analyzed, the mean age was 61 years old, and 62% of the cohort were males. Lower baseline hemoglobin levels are associated with increased odds of hematoma expansion (adjusted odds ratio per -1 g/dL hemoglobin decrement, 1.10 [95% CI, 1.02-1.19]) and poor 3-month clinical outcomes (adjusted odds ratio per -1 g/dL hemoglobin decrement, 1.11 [95% CI, 1.03-1.21]). Similar relationships were seen with poor 6- and 12-month outcomes. In our animal model, anemic mice had significantly greater ICH lesion expansion, 24-hour lesion volumes, and greater mortality, as compared with nonanemic mice.

Conclusions: These results, in a human cohort and a mouse model, provide novel evidence suggesting that anemia has causal roles in hematoma expansion and poor ICH outcomes. Additional studies are required to clarify whether correcting anemia can improve these outcomes.

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低血红蛋白导致血肿扩张和脑出血预后不良。
背景:虽然较低的血红蛋白水平与较严重的脑出血(ICH)结局相关,但这种关系的因果因素尚不清楚。我们利用人类观察数据研究了低血红蛋白与血肿扩张风险增加和预后不良相关的假设,并利用贫血和脑出血的小鼠模型评估了因果关系。方法:对2010年至2016年间入选的2997例脑出血患者进行多中心前瞻性观察队列研究。基线血红蛋白测量和连续计算机断层神经成像的患者被纳入分析。排除有全身性凝血功能障碍的患者。在调整相关协变量后,单独的回归模型评估了基线血红蛋白与血肿扩张(≥33%和/或≥6ml生长)和不良长期神经预后(改良Rankin量表评分为4-6)的关系。采用小鼠胶原酶脑出血模型,对贫血与非贫血C57/BL6小鼠进行一系列神经成像,评估脑出血病变体积、病变体积变化和早期死亡率的组间差异。结果:分析1190例脑出血患者,平均年龄61岁,62%为男性。较低的基线血红蛋白水平与血肿扩大的几率增加(每-1 g/dL血红蛋白减少的校正优势比,1.10 [95% CI, 1.02-1.19])和3个月的不良临床结果相关(每-1 g/dL血红蛋白减少的校正优势比,1.11 [95% CI, 1.03-1.21])。6个月和12个月的不良结果也存在类似的关系。在我们的动物模型中,与非贫血小鼠相比,贫血小鼠的脑出血病变扩张、24小时病变体积和死亡率明显更大。结论:这些在人类队列和小鼠模型中的结果提供了新的证据,表明贫血在血肿扩大和脑出血预后不良中起因果作用。需要进一步的研究来阐明纠正贫血是否可以改善这些结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Stroke
Stroke 医学-临床神经学
CiteScore
13.40
自引率
6.00%
发文量
2021
审稿时长
3 months
期刊介绍: Stroke is a monthly publication that collates reports of clinical and basic investigation of any aspect of the cerebral circulation and its diseases. The publication covers a wide range of disciplines including anesthesiology, critical care medicine, epidemiology, internal medicine, neurology, neuro-ophthalmology, neuropathology, neuropsychology, neurosurgery, nuclear medicine, nursing, radiology, rehabilitation, speech pathology, vascular physiology, and vascular surgery. The audience of Stroke includes neurologists, basic scientists, cardiologists, vascular surgeons, internists, interventionalists, neurosurgeons, nurses, and physiatrists. Stroke is indexed in Biological Abstracts, BIOSIS, CAB Abstracts, Chemical Abstracts, CINAHL, Current Contents, Embase, MEDLINE, and Science Citation Index Expanded.
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