对巴西成年镰状细胞病患者进行蒙特利尔认知评估:不良社会文化背景的负担

EJHaem Pub Date : 2024-03-28 DOI:10.1002/jha2.875
Pedro Junqueira Fleury Silva, Caroline Martins Silva, Brunno Machado de Campos, Paula de Melo Campos, Samuel de Souza Medina, Andreza Lamonica, José Vitor Coimbra Trindade, Fernando Cendes, Fernando Ferreira Costa, Sara Teresinha Olalla Saad, Bruno Deltreggia Benites
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引用次数: 0

摘要

镰状细胞病(SCD)患者罹患无声脑梗塞和明显中风的风险较高,这可能会导致认知功能受损、功能受限和生活质量下降。我们通过蒙特利尔认知评估(MoCA)对巴西成年 SCD 患者(n = 124;19-70 岁;56 名男性;79 名 SS,28 名 SC,10 名 S/β0,7 名 S/β+)的认知功能进行了筛查,并将筛查结果与可能影响测试成绩的预测因素(包括社会文化、临床、实验室数据和脑成像)相关联。MoCA 得分的中位数为 23 分(8-30 分);70% 的人得分在 25 分或以下,表明存在一定程度的认知障碍。在 SS 和 SC 患者中,MoCA 结果与任何临床或实验室数据均无明显关联;但在 HbS/β 地中海贫血症患者中,MoCA 结果与中风有明显关联(P = 0.03)。根据社会人口学条件,如年龄(r = -0.316; P < 0.001)、首次工作年龄(r = 0.221; P = 0.018)、个人(r = 0.23; P = 0.012)和熟悉的人均收入(r = 0.303; P = 0.001)、个人(r = 0.61; P = 0)、母亲(r = 0.536; P = 0)和父亲的教育状况(r = 0.441; P = 0)。我们使用多变量回归进一步寻找预测表现的独立因素,结果发现受教育程度越高,MoCA得分越高(0.8099,95% 置信区间 [CI]:0.509-1.111)。脑成像分析显示,与记忆、学习和执行功能相关的重要脑区出现了明显的进行性萎缩。这些数据表明,成年 SCD 患者认知能力下降的发生率高且影响大,脑萎缩区域也反映了这一点。我们还可以观察到社会人口条件对患者认知能力的影响,以及针对这些缺陷制定有针对性的治疗计划的必要性。此外,在 SS 组和 SC 组中,MoCA 值与中风没有明显的相关性,这可能与巴西非洲裔人口最恶劣的社会文化和经济条件有关,其中低教育刺激对认知功能的影响甚至超过了疾病造成的解剖损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Montreal cognitive assessment in Brazilian adults with sickle cell disease: The burdens of poor sociocultural background

Montreal cognitive assessment in Brazilian adults with sickle cell disease: The burdens of poor sociocultural background

Sickle cell disease (SCD) patients are at higher risk of developing silent cerebral infarcts and overt stroke, which may reflect cognitive impairment, functional limitations, and worse quality of life. The cognitive function of Brazilian adult SCD patients (n = 124; 19–70 years; 56 men; 79 SS, 28 SC, 10 S/β0, 7 S/β+) was screened through Montreal Cognitive Assessment (MoCA) and correlated the results with possible predictive factors for test performance, including sociocultural, clinical, laboratory data and brain imaging. The Median MoCA score was 23 (8–30); 70% had a 25-or-less score, suggesting some level of cognitive impairment. There were no significant associations between MoCA results and any clinical or laboratory data in SS and SC patients; however, a significant correlation (P = 0.03) with stroke was found in HbS/β-thalassemic patients. Correlations were further detected according to sociodemographic conditions, such as age (= −0.316; P < 0.001), age at first job (r = 0.221; P = 0.018), personal (r = 0.23; P = 0.012) and per capita familiar incomes (r = 0.303; P = 0.001), personal (r = 0.61; P = 0), maternal (r = 0.536; P = 0), and paternal educational status (r = 0.441; P = 0). We further sought independent predictors of performance using multivariable regressions and increased education was an independent predictor of better scores in MoCA (0.8099, 95% confidence interval [CI]: 0.509–1.111). Brain imaging analysis showed significant and progressive atrophy in important cerebral areas related to memory, learning, and executive function. These data point to the high prevalence and impact of cognitive decline in adult SCD patients, mirrored in brain atrophic areas. It is also possible to observe the influence of sociodemographic conditions on patients’ cognitive performances and the need for creating focused therapeutic plans that address these deficiencies. Moreover, the absence of a significant correlation of MoCA values with stroke in the SS and SC groups may be related to the worst sociocultural and economic conditions of the Brazilian African descent population, in which the impact of low educational stimulation on cognitive function can outweigh even the anatomical damage caused by the disease.

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