Factors associated with cognitive function in patient with Alzheimer's disease with newly prescribed acetylcholinesterase inhibitors: A 1‐year retrospective cohort study

Author:

Ching Pao‐Yuan1ORCID,Chang Cheng‐Ho1,Pan Chih‐Chuan12,Chiang Yung‐Chih1,Kuo Hsin‐ya12,Hsu Tien‐Wei345ORCID,Chu Che‐Sheng1267ORCID

Affiliation:

1. Department of Psychiatry Kaohsiung Veterans General Hospital Kaohsiung Taiwan

2. Center for Geriatric and Gerontology Kaohsiung Veterans General Hospital Kaohsiung Taiwan

3. Department of Psychiatry, E‐DA Dachang Hospital I‐Shou University Kaohsiung Taiwan

4. Department of Psychiatry, E‐DA Hospital I‐Shou University Kaohsiung Taiwan

5. Graduate Institute of Clinical Medicine, College of Medicine Kaohsiung Medical University Kaohsiung Taiwan

6. Non‐invasive Neuromodulation Consortium for Mental Disorders Society of Psychophysiology Taipei Taiwan

7. Graduate Institute of Medicine, College of Medicine Kaohsiung Medical University Kaohsiung Taiwan

Abstract

AbstractObjectiveWe aimed to examine the factors associated with treatment outcomes in patients with Alzheimer's disease (AD) after 1 year of acetylcholinesterase inhibitors (AChEI) treatment.MethodWe obtained electronic medical records from a medical center in Southern Taiwan between January 2015 and September 2021. Participants aged ≥60 who were newly diagnosed with AD and had been prescribed AChEIs were included. Cognitive assessments were performed before the AChEIs were prescribed and at the 1 year follow‐up. Cognition progressors were defined as a Mini‐Mental State Examination decline of >3 or a Clinical Dementia Rating decline of ≥1 after 1 year of AChEI treatment. The relationship between the baseline characteristics and cognitive status after follow‐up was investigated using logistic regression analysis after adjusting for potential confounders.ResultsA total of 1370 patients were included in our study (mean age, 79.86 ± 8.14 years). After adjustment, the body mass index (BMI) was found to be significantly lower in the progressor group [adjusted odds ratio (AOR): 0.970, 95% confidence intervals (95% CIs): 0.943 to 0.997, P = 0.033]. The usage of antipsychotics was significantly higher in the progressor group (AOR: 1.599, 95% CIs: 1.202 to 2.202, P = 0.001). The usage of benzodiazepine receptor agonists also tended to be significantly higher in the progressor group (AOR: 1.290, 95% CIs: 0.996 to 1.697, p = 0.054).ConclusionThese results suggest that patients with AD who receive 1 year of AChEI treatment and have a lower BMI or concurrent treatment with antipsychotics and benzodiazepine receptor agonists are more likely to suffer from cognitive decline.

Publisher

Wiley

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