The College of Arts and Sciences, University of Washington, Seattle.
Division of General Internal Medicine, Department of Medicine, University of Washington, Seattle.
JAMA Otolaryngol Head Neck Surg. 2022 Jan 1;148(1):20-27. doi: 10.1001/jamaoto.2021.2716.
Age-related hearing difficulties can include problems with signal audibility and central auditory processing. Studies have demonstrated associations between audibility and dementia risk. To our knowledge, limited data exist to determine whether audibility, central processing, or both drive these associations.
To determine the associations between signal sensitivity, central auditory processing, and dementia and Alzheimer dementia (AD) risk.
DESIGN, SETTING, AND PARTICIPANTS: This follow-up observational study of a sample from the prospective Adult Changes in Thought study of dementia risk was conducted at Kaiser Permanente Washington, a western Washington health care delivery system, and included 280 volunteer participants without dementia who were evaluated from October 2003 to February 2006 with follow-up through September 2018. Analyses began in 2019 and continued through 2021.
Hearing tests included pure tone signal audibility, a monaural word recognition test, and 2 dichotic tests: the Dichotic Sentence Identification (DSI) test and the Dichotic Digits test (DDT).
Cognition was assessed biennially with the Cognitive Abilities Screening Instrument (range, 1-100; higher scores are better), and scores of less than 86 prompted clinical and neuropsychological evaluations. All data were reviewed at multidisciplinary consensus conferences, and standardized criteria were used to define incident cases of dementia and probable or possible AD. Cox proportional hazard models were used to determine associations with hearing test performance.
A total of 280 participants (177 women [63%]; mean [SD] age, 79.5 [5.2] years). As of September 2018, there were 2196 person-years of follow-up (mean, 7.8 years) and 89 incident cases of dementia (66 not previously analyzed), of which 84 (94.4%) were AD (63 not previously analyzed). Compared with people with DSI scores of more than 80, the dementia adjusted hazard ratio (aHR) for DSI scores of less than 50 was 4.18 (95% CI, 2.37-7.38; P < .001); for a DSI score of 50 to 80, it was 1.82 (95% CI, 1.10-3.04; P = .02). Compared with people with DDT scores of more than 80, the dementia aHR for DDT scores of less than 50 was 2.66 (95% CI, 1.31-5.42; P = .01); for a DDT score of 50 to 80, it was 2.40 (95% CI, 1.45-3.98; P = .001). The AD results were similar. Pure tone averages were weakly and insignificantly associated with dementia and AD, and associations were null when controlling for DSI scores.
In this cohort study, abnormal central auditory processing as measured by dichotic tests was independently associated with dementia and AD risk.
与年龄相关的听力障碍可能包括信号可听度和中枢听觉处理方面的问题。研究已经证明了可听度与痴呆风险之间的关联。据我们所知,目前还没有足够的数据来确定可听度、中枢处理或两者共同驱动这些关联。
确定信号灵敏度、中枢听觉处理与痴呆和阿尔茨海默病(AD)风险之间的关系。
设计、地点和参与者:这是一项对痴呆风险前瞻性成人思维变化研究中样本的随访观察性研究,在华盛顿西部的 Kaiser Permanente Washington 医疗保健系统进行,纳入了 280 名无痴呆症的志愿者参与者,他们于 2003 年 10 月至 2006 年 2 月接受评估,并随访至 2018 年 9 月。分析于 2019 年开始,并持续到 2021 年。
听力测试包括纯音信号可听度、单耳单词识别测试以及 2 项双耳测试:双耳句子识别测试(DSI)和双耳数字测试(DDT)。
认知能力每两年通过认知能力筛查工具(范围为 1-100;分数越高越好)进行评估,如果分数低于 86,则进行临床和神经心理学评估。所有数据均在多学科共识会议上进行审查,并使用标准化标准定义痴呆症和可能或可能的 AD 的新发病例。Cox 比例风险模型用于确定与听力测试表现的关联。
共有 280 名参与者(177 名女性[63%];平均[标准差]年龄为 79.5[5.2]岁)。截至 2018 年 9 月,有 2196 人年的随访时间(平均 7.8 年)和 89 例痴呆症(66 例以前未分析)的新发病例,其中 84 例(94.4%)为 AD(66 例以前未分析)。与 DSI 得分高于 80 的人相比,DSI 得分低于 50 的痴呆症调整后的危险比(aHR)为 4.18(95%CI,2.37-7.38;P<0.001);DSI 得分为 50-80 的 aHR 为 1.82(95%CI,1.10-3.04;P=0.02)。与 DDT 得分高于 80 的人相比,DDT 得分低于 50 的痴呆症 aHR 为 2.66(95%CI,1.31-5.42;P=0.01);DDT 得分为 50-80 的 aHR 为 2.40(95%CI,1.45-3.98;P=0.001)。AD 的结果相似。纯音平均值与痴呆症和 AD 的相关性较弱且无统计学意义,并且在控制 DSI 分数后相关性为零。
在这项队列研究中,通过双耳测试测量的异常中枢听觉处理与痴呆症和 AD 风险独立相关。