认知变化在识别同种异体造血细胞移植后急性移植物抗宿主病中的应用

J. Stratton, Allison Sylvia, F. Hoodin, S. Choi, A. Pawarode, B. Giordani, K. Votruba
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摘要

摘要目的:急性移植物抗宿主病(aGVHD)是同种异体造血细胞移植(HCT)的常见并发症,与发病率和死亡率相关。识别那些有发展aGVHD风险的人对于早期干预至关重要。目前的研究评估了一项简短的认知筛查措施的得分是否可以在hct后100天识别出那些发展为aGVHD的患者。方法:参与者为37例接受同种异体HCT的患者,分别在移植前、移植后30天和100天进行评估。在完成所有评估的患者中,将患者分为在hct后第100天发生aGVHD的患者(n = 14)和未发生aGVHD的患者(n = 16)。移植后100天,各组在相关人口统计学因素、疾病、调节方案、供体相关性、干细胞来源、类固醇使用、全身照射使用、人类白细胞抗原(HLA)匹配或感染频率方面没有差异。结果:在hct后100天,aGVHD患者在工作记忆测试中的表现明显差于没有aGVHD的患者。第100天aGVHD的存在显著增加,工作记忆从基线到hct后30天每降低一个标准差(优势比= 3.08;95% ci: 1.00-9.36)。尽管样本量小,并对多重分析进行了统计控制,但仍观察到这些发现。结论:虽然这项研究本质上是探索性的,而且样本量很小,但研究结果表明,早期发现工作记忆衰退可能与aGVHD的发展相吻合,或者预示着aGVHD的发展。讨论了潜在的病因。在hct后的前30天内实施早期认知筛查可能有助于识别有aGVHD风险的患者。
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The utility of cognitive changes in identifying those with acute graft vs. host disease following allogeneic hematopoietic cell transplant
Abstract Objectives: Acute graft versus host disease (aGVHD) is a common complication of allogeneic hematopoietic cell transplant (HCT) and is associated with morbidity and mortality. Identifying those at risk for developing aGVHD is crucial for early intervention. The current study assessed whether scores on a brief cognitive screening measure could identify those that develop aGVHD by 100 days post-HCT. Methods: Participants were 37 patients undergoing allogeneic HCT, assessed prior to transplant, and at 30- and 100-days post-HCT. Of those completing all evaluations, patients were divided into those who did (n = 14) and did not (n = 16) develop aGVHD by day 100 post-HCT. At 100 days post-transplant, groups did not differ on relevant demographic factors, disease, conditioning regimen, relatedness of donor, stem cell source, steroid use, total body irradiation use, human leukocyte antigens (HLA) match, or frequency of infection. Results: At 100 days post-HCT, those with aGVHD performed significantly worse on a working memory measure than those without aGvHD. The presence of aGVHD at day 100 increased significantly with every one standard deviation decrease in working memory from baseline to 30 days post-HCT (odds ratio = 3.08; 95% CI: 1.00–9.36). These findings were observed despite a small sample size and statistically controlling for multiple analyses. Conclusions: While this study is exploratory in nature, and has a small sample size, findings suggest that early detection of working memory declines could coincide with, or signal the development of, aGVHD. Potential etiologies are discussed. Implementing early cognitive screening within the first 30 days post-HCT may be useful in identifying patients at risk for aGVHD.
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