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PSEN1-E280A基因变异所致早发性常染色体显性阿尔茨海默病患者的营养评估:一项横断面研究

Nutritional Assessment in Patients with Early-Onset Autosomal Dominant Alzheimer's Disease Due to PSEN1- E280A Genetic Variant: A Cross-Sectional Study.

作者信息

Gómez-Vega M, Garcia-Cifuentes E, Aguillon D, Velez J E, Jaramillo-Jimenez A, Vasquez D, Gómez-Henck C, Andrés Tobon C, Deossa Restrepo G C, Lopera F

机构信息

Grupo Neuropsicología y Conducta, Facultad de Medicina, Universidad de Antioquia, Institución Prestadora de Servicios de Salud - IPS Universitaria, Medellín, Colombia.

Grupo Neurociencias de Antioquia, Facultad de Medicina, Universidad de Antioquia, Medellín, Colombia.

出版信息

JAR Life. 2021 Jun 6;10:32-38. doi: 10.14283/jarlife.2021.6. eCollection 2021.

Abstract

BACKGROUND

Weight loss and malnutrition are frequent findings in late-onset and sporadic presentations of Alzheimer's Disease (AD). However, less is known about nutritional status in Early-Onset Autosomal Dominant AD (EO-ADAD).

OBJECTIVE

To analyze the association between nutritional status and other clinical and sociodemographic characteristics in individuals with a genetic form of EO-ADAD.

DESIGN SETTINGS AND PARTICIPANTS

Cross-sectional study with 75 non-institutionalized participants from a cohort of Autosomal Dominant AD (13 with mild cognitive impairment and 61 with dementia, ages from 38 to 67 years) underwent a structured clinical assessment with emphasis on nutritional status.

MEASUREMENTS

Primary outcome was nutritional status and it was measured using the Mini Nutritional Assessment (MNA). Patients were categorized according to MNA total score, as undernourished (MNA ≤23.5) and well-nourished (MNA ≥ 24). Sociodemographic and clinical variables identified as potential predictors or confounders of nutritional status were also collected.

RESULTS

Undernourishment by MNA was present in 57.3% of the sample. Forty-two percent of participants had abnormal BMI values considered lower than 18.5 or higher than 24.9 kg/m2. Total BMI values were similar in well and undernourished patients (median 24.2 IQR 3.59 and median 23.9 IQR 4.42, respectively, p=0.476). When comparing well and undernourished groups, we found statistically significant differences for variables: severity of dementia (p=0.034), frailty (p=0.001), multimorbidity (p=0.035) and, polymedication (p=0.045). Neither adjusted logistic regression nor the Poisson regression showed that any clinical or sociodemographic variables explained undernourishment.

CONCLUSIONS

Undernourishment was a frequent finding in our sample of EO-ADAD, especially in later stages of the disease. Patients with polymedication, multimorbidity, frailty and severe dementia show differences in their nutritional status with a tendency to be more frequently undernourished. Further studies with larger sample sizes are needed to establish this association.

摘要

背景

体重减轻和营养不良在晚发型和散发性阿尔茨海默病(AD)中很常见。然而,对于早发型常染色体显性AD(EO-ADAD)的营养状况了解较少。

目的

分析EO-ADAD遗传形式个体的营养状况与其他临床和社会人口学特征之间的关联。

设计、场所和参与者:对来自常染色体显性AD队列的75名非机构化参与者进行横断面研究(13名轻度认知障碍者和61名痴呆症患者,年龄38至67岁),进行了以营养状况为重点的结构化临床评估。

测量

主要结局是营养状况,使用微型营养评定法(MNA)进行测量。根据MNA总分将患者分为营养不良(MNA≤23.5)和营养良好(MNA≥24)。还收集了被确定为营养状况潜在预测因素或混杂因素的社会人口学和临床变量。

结果

样本中57.3%的人存在MNA评定的营养不良。42%的参与者BMI值异常,被认为低于18.5或高于24.9kg/m²。营养良好和营养不良患者的总BMI值相似(中位数分别为24.2,四分位间距3.59和中位数23.9,四分位间距4.42,p=0.476)。在比较营养良好和营养不良组时,我们发现以下变量存在统计学显著差异:痴呆严重程度(p=0.034)、虚弱(p=0.001)、多种疾病(p=0.035)和多种药物治疗(p=0.045)。调整后的逻辑回归和泊松回归均未显示任何临床或社会人口学变量可解释营养不良情况。

结论

在我们的EO-ADAD样本中,营养不良很常见,尤其是在疾病后期。使用多种药物、患有多种疾病、身体虚弱和患有严重痴呆症的患者在营养状况方面存在差异,营养不良的倾向更频繁。需要进行更大样本量的进一步研究来确定这种关联。

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