与过敏相关和非过敏相关的老年人嗅觉障碍与认知功能的关系:两项横断面研究

Hui Chen, Yihong Ding, Liyan Huang, Wansi Zhong, Xiaojun Lin, Baoyue Zhang, Yan Zheng, Xin Xu, Min Lou, Changzheng Yuan
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引用次数: 0

摘要

背景:嗅觉障碍(OI)与年龄相关的认知能力下降之间的关系尚无定论,过敏的潜在影响仍不明确:我们旨在评估与过敏相关和非过敏相关的 OI 与认知功能的横断面关联:我们纳入了健康与退休研究(HRS)--统一认知评估协议(HCAP)子研究的 2499 名参与者和英国老龄化纵向研究(ELSA)--HCAP 的 1086 名参与者。使用 Sniffin' Stick 气味笔进行嗅觉功能现场检查 (OFFE),以客观评估嗅觉功能和嗅觉评分结果:与非 OI 参与者相比,OI 患者的 MMSE z 评分较低[βHRS = -0.33,95% 置信区间 (CI):-0.41 至 -0.24;βELSA = -0.31,-0.43 至 -0.18],认知障碍患病率较高[患病率比 (PR)HRS = 1.46,1.06 至 2.01;PRELSA = 1.63,1.26 至 2.11]。非过敏相关 OI 的相关性(βHRS = -0.36;βELSA = -0.34)强于过敏相关 OI(βHRS = -0.26;βELSA = 0.13)。在特定领域的认知功能测量中也观察到类似的关联:结论:OI,尤其是非过敏相关的 OI,与老年人较差的认知功能有关。尽管目前的横断面研究存在一些局限性,如反向因果关系和残余混杂因素,但研究结果将有助于深入了解OI与认知功能的关系,并启发人们今后关注非过敏相关OI,以预防潜在的认知功能损害。
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The Association of Allergy-Related and Non-Allergy-Related Olfactory Impairment with Cognitive Function in Older Adults: Two Cross- Sectional Studies.

Background: Evidence on the association of Olfactory Impairment (OI) with age-related cognitive decline is inconclusive, and the potential influence of allergy remains unclear.

Objective: We aimed to evaluate the cross-sectional associations of allergy-related and non-allergy- related OI to cognitive function.

Methods: We included 2,499 participants from the Health and Retirement Study (HRS)-Harmonized Cognitive Assessment Protocol (HCAP) sub-study and 1,086 participants from the English Longitudinal Study of Ageing (ELSA)-HCAP. The Olfactory Function Field Exam (OFFE) using Sniffin' Stick odor pens was used to objectively assess olfactory function and an olfactory score <6/11 indicated OI. Mini-Mental Status Examination (MMSE) was used to assess global cognitive function and define cognitive impairment (<24/30). A neuropsychologic battery was used to assess five cognitive domains.

Results: Compared to non-OI participants, individuals with OI had lower MMSE z-score [βHRS = -0.33, 95% Confidence Interval (CI): -0.41 to -0.24; βELSA = -0.31, -0.43 to -0.18] and higher prevalence of cognitive impairment (Prevalence Ratio (PR)HRS = 1.46, 1.06 to 2.01; PRELSA = 1.63, 1.26 to 2.11). The associations were stronger for non-allergy-related OI (βHRS = -0.36; βELSA = -0.34) than for allergy-related OI (βHRS = -0.26; βELSA = 0.13). Similar associations were observed with domain- specific cognitive function measures.

Conclusion: OI, particularly non-allergy-related OI, was related to poorer cognitive function in older adults. Although the current cross-sectional study is subject to several limitations, such as reverse causality and residual confounding, the findings will provide insights into the OI-cognition association and enlighten future attention to non-allergy-related OI for the prevention of potential cognitive impairment.

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