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Prevalence and affective correlates of subjective cognitive decline in patients with de novo Parkinson's disease

OBJECTIVES: The novel concept of subjective cognitive decline (SCD) in Parkinson's disease (PD) refers to subjective cognitive impairment without concurrent objective cognitive deficits. This study aimed to determine the prevalence and affective correlates of SCD in de novo PD patients. MATERIA...

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Autores principales: Yang, Ning, Ju, Yuanyuan, Ren, Jingru, Wang, Haidong, Li, Peishan, Ning, Houxu, Tao, Jiaping, Liu, Weiguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545461/
https://www.ncbi.nlm.nih.gov/pubmed/35722712
http://dx.doi.org/10.1111/ane.13662
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author Yang, Ning
Ju, Yuanyuan
Ren, Jingru
Wang, Haidong
Li, Peishan
Ning, Houxu
Tao, Jiaping
Liu, Weiguo
author_facet Yang, Ning
Ju, Yuanyuan
Ren, Jingru
Wang, Haidong
Li, Peishan
Ning, Houxu
Tao, Jiaping
Liu, Weiguo
author_sort Yang, Ning
collection PubMed
description OBJECTIVES: The novel concept of subjective cognitive decline (SCD) in Parkinson's disease (PD) refers to subjective cognitive impairment without concurrent objective cognitive deficits. This study aimed to determine the prevalence and affective correlates of SCD in de novo PD patients. MATERIALS AND METHODS: A total of 139 de novo PD patients underwent comprehensive neuropsychological evaluation. PD patients with SCD (PD‐SCD) did not meet the diagnostic criteria for mild cognitive impairment in PD (PD‐MCI) based on the Movement Disorder Society Level II Criteria and were defined by a Domain‐5 Score ≥1 on the Non‐Motor Symptoms Questionnaire. Affective symptoms were measured using the Hamilton Depression Scale (HAMD) and Hamilton Anxiety Scale (HAMA). RESULTS: In de novo PD cohort, the prevalence of SCD was 28.1%. PD‐SCD patients performed significantly better than PD‐MCI patients on tests of five cognitive domains. The more commonly affected domains in PD‐SCD patients were memory (28.2%) and attention/working memory (25.6%). Multivariable linear regression analysis revealed that PD‐SCD was significantly associated with both HAMD (β = 4.518, 95% CI = 0.754–8.281, p = .019) and HAMA scores (β = 4.259, 95% CI = 1.054–7.464, p = .010). Furthermore, binary logistic regression analysis revealed that higher HAMD (OR = 1.128, 95% CI = 1.019–1.249, p = .020) and HAMA scores (OR = 1.176, 95% CI = 1.030–1.343, p = .017) increased the risk of PD‐SCD. CONCLUSIONS: Our findings suggest that SCD is highly prevalent in de novo PD patients. The presence of PD‐SCD is suggestive of an underlying affective disorder.
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spelling pubmed-95454612022-10-14 Prevalence and affective correlates of subjective cognitive decline in patients with de novo Parkinson's disease Yang, Ning Ju, Yuanyuan Ren, Jingru Wang, Haidong Li, Peishan Ning, Houxu Tao, Jiaping Liu, Weiguo Acta Neurol Scand Original Articles OBJECTIVES: The novel concept of subjective cognitive decline (SCD) in Parkinson's disease (PD) refers to subjective cognitive impairment without concurrent objective cognitive deficits. This study aimed to determine the prevalence and affective correlates of SCD in de novo PD patients. MATERIALS AND METHODS: A total of 139 de novo PD patients underwent comprehensive neuropsychological evaluation. PD patients with SCD (PD‐SCD) did not meet the diagnostic criteria for mild cognitive impairment in PD (PD‐MCI) based on the Movement Disorder Society Level II Criteria and were defined by a Domain‐5 Score ≥1 on the Non‐Motor Symptoms Questionnaire. Affective symptoms were measured using the Hamilton Depression Scale (HAMD) and Hamilton Anxiety Scale (HAMA). RESULTS: In de novo PD cohort, the prevalence of SCD was 28.1%. PD‐SCD patients performed significantly better than PD‐MCI patients on tests of five cognitive domains. The more commonly affected domains in PD‐SCD patients were memory (28.2%) and attention/working memory (25.6%). Multivariable linear regression analysis revealed that PD‐SCD was significantly associated with both HAMD (β = 4.518, 95% CI = 0.754–8.281, p = .019) and HAMA scores (β = 4.259, 95% CI = 1.054–7.464, p = .010). Furthermore, binary logistic regression analysis revealed that higher HAMD (OR = 1.128, 95% CI = 1.019–1.249, p = .020) and HAMA scores (OR = 1.176, 95% CI = 1.030–1.343, p = .017) increased the risk of PD‐SCD. CONCLUSIONS: Our findings suggest that SCD is highly prevalent in de novo PD patients. The presence of PD‐SCD is suggestive of an underlying affective disorder. John Wiley and Sons Inc. 2022-06-20 2022-09 /pmc/articles/PMC9545461/ /pubmed/35722712 http://dx.doi.org/10.1111/ane.13662 Text en © 2022 The Authors. Acta Neurologica Scandinavica published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Yang, Ning
Ju, Yuanyuan
Ren, Jingru
Wang, Haidong
Li, Peishan
Ning, Houxu
Tao, Jiaping
Liu, Weiguo
Prevalence and affective correlates of subjective cognitive decline in patients with de novo Parkinson's disease
title Prevalence and affective correlates of subjective cognitive decline in patients with de novo Parkinson's disease
title_full Prevalence and affective correlates of subjective cognitive decline in patients with de novo Parkinson's disease
title_fullStr Prevalence and affective correlates of subjective cognitive decline in patients with de novo Parkinson's disease
title_full_unstemmed Prevalence and affective correlates of subjective cognitive decline in patients with de novo Parkinson's disease
title_short Prevalence and affective correlates of subjective cognitive decline in patients with de novo Parkinson's disease
title_sort prevalence and affective correlates of subjective cognitive decline in patients with de novo parkinson's disease
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545461/
https://www.ncbi.nlm.nih.gov/pubmed/35722712
http://dx.doi.org/10.1111/ane.13662
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