Izquierdo Delgado E, Gutiérrez Ríos R, Andrés Calvo M, Repiso Gento I, Castrillo Sanz A, Rodríguez Herrero R, Rodríguez Sanz M F, Tola-Arribas M A
Servicio de Medicina Interna, Hospital Universitario Río Hortega, Valladolid, España.
Sección de Neurología, Complejo Asistencial de Segovia, Segovia, España.
Neurologia (Engl Ed). 2020 Jan 21. doi: 10.1016/j.nrl.2019.11.005.
Nutritional deficiencies are frequent in Alzheimer disease (AD), even in early stages. Nutritional impairment (NI) may be associated with faster disease progression. The objective of this study was to describe the frequency of NI and the associated risk factors at the time of diagnosis and to analyse its influence on subsequent progression.
We performed a prospective, multicentre, observational study of patients recently diagnosed with prodromal AD (pAD) or dementia due to AD (ADd). Two clinical assessments were conducted over a period of 18months. The Mini Nutritional Assessment test (MNA; score range, 0-30; cut-off point for NI, <24) was used to estimate nutritional status. Progression was defined as an increase of ≥3points on the Clinical Dementia Rating-sum of boxes test.
The sample included 50 patients with pAD (mean [standard deviation] age, 76.1 [5.3] years; 68% women), and 127 with ADd (80 [5.9] years; 72.4% women). A total of 141 (79.7%) completed both evaluations. The prevalence of NI was 28.2% (24% for pAD, 29.9% for ADd; P=.43), with the majority (92%) at risk of malnutrition. NI was associated with female sex (odds ratio [OR]: 4.2; 95% confidence interval [CI]: 1.7-10.5; P<.001) and greater behavioural involvement (OR: 5.8; 95%CI: 2.6-12.7; P<.001). A larger proportion of patients with progression was observed among those with NI than among those with normal nutritional status (50% vs 28.7%, P<.05; ADd: 53.6% vs 31.8%, P<.05; pAD: 41.7% vs 22.9%, P=.21). Greater cognitive impairment (OR: 2.1; 95%CI: 1.03-4.4; P<.05) and NI (OR: 2.4; 95%CI: 1.1-5.1; P<.05) were independent risk factors for disease progression.
NI is highly prevalent in patients with AD. Assessing nutritional status at the time of diagnosis may enable identification of patients at greater risk of disease progression.
营养缺乏在阿尔茨海默病(AD)中很常见,即使在疾病早期也是如此。营养损害(NI)可能与疾病进展加快有关。本研究的目的是描述诊断时NI的发生率及其相关危险因素,并分析其对后续疾病进展的影响。
我们对近期诊断为前驱期AD(pAD)或AD所致痴呆(ADd)的患者进行了一项前瞻性、多中心观察性研究。在18个月的时间里进行了两次临床评估。采用微型营养评定法(MNA;评分范围为0 - 30分;NI的临界值为<24分)来评估营养状况。疾病进展定义为临床痴呆评定量表总分测试得分增加≥3分。
样本包括50例pAD患者(平均[标准差]年龄为76.1[5.3]岁;68%为女性)和127例ADd患者(80[5.9]岁;72.4%为女性)。共有141例(79.7%)患者完成了两次评估。NI的患病率为28.2%(pAD为24%,ADd为29.9%;P = 0.43),其中大多数(92%)存在营养不良风险。NI与女性性别(优势比[OR]:4.2;95%置信区间[CI]:1.7 - 10.5;P < 0.001)和更多的行为问题(OR:5.8;95%CI:2.6 - 12.7;P < 0.001)相关。与营养状况正常的患者相比,NI患者中疾病进展的比例更高(50%对28.7%,P < 0.05;ADd:53.6%对31.8%,P < 0.05;pAD:41.7%对22.9%;P = 0.21)。更严重的认知障碍(OR:2.1;95%CI:1.03 - 4.4;P < 0.05)和NI(OR:2.4;95%CI:1.1 - 5.1;P < 0.05)是疾病进展的独立危险因素。
NI在AD患者中非常普遍。在诊断时评估营养状况可能有助于识别疾病进展风险更高的患者。