Use of biomarkers in the diagnosis of Alzheimer’s disease in adults with intellectual disability

IF 13.4 Q1 GERIATRICS & GERONTOLOGY Lancet Healthy Longevity Pub Date : 2024-10-01 DOI:10.1016/j.lanhl.2024.100639
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Abstract

People with intellectual disability are a vulnerable cohort who face challenges accessing health care. Compared with the general population, people with intellectual disability have an elevated risk of developing dementia, which often presents at a younger age and with atypical symptoms. The lifelong cognitive and functional difficulties faced by people with intellectual disability further complicate the diagnostic process. Specialised intellectual disability memory services and evaluation using reliable biomarkers of neurodegeneration are needed to improve diagnostic and prognostic certainty in this group. Inadequate specialist services and paucity of research on biomarkers in this population hinders progress and impedes the delivery of adequate health care. Although cerebrospinal fluid-based biomarkers and radiological biomarkers are used routinely in the evaluation of Alzheimer’s disease in the general population, biological variation within the clinically heterogenous group of people with intellectual disability could affect the clinical utility of existing biomarkers. As disease-modifying therapies become available for the treatment of early Alzheimer’s disease, and hopefully other neurodegenerative conditions in the future, biomarkers will serve as gatekeepers to establish the eligibility for such therapies. Inadequate representation of adults with intellectual disability in biomarker research will result in their exclusion from treatment with disease-modifying therapies, thus perpetuating the inequity in health care that is already faced by this group. The aim of this Series paper is to summarise current evidence on the application of biomarkers for Alzheimer’s disease in a population with intellectual disability (that is not attributable to Down syndrome) and suspected cognitive decline.
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使用生物标志物诊断智障成人阿尔茨海默病。
智障人士是弱势群体,他们在获得医疗保健服务方面面临挑战。与普通人群相比,智障人士罹患痴呆症的风险更高,而且痴呆症的发病年龄往往更小,症状也不典型。智障人士终生面临的认知和功能障碍使诊断过程更加复杂。需要提供专门的智障记忆服务,并使用可靠的神经变性生物标志物进行评估,以提高该群体诊断和预后的确定性。专科服务的不足和对这一人群生物标志物研究的匮乏阻碍了进展,并妨碍了提供适当的医疗保健服务。虽然基于脑脊液的生物标志物和放射学生物标志物已被常规用于评估普通人群中的阿尔茨海默病,但在临床上具有异质性的智障人士群体中的生物变异可能会影响现有生物标志物的临床效用。随着可用于治疗早期阿尔茨海默病的疾病改变疗法的出现,以及希望将来能用于治疗其他神经退行性疾病,生物标志物将成为确定是否有资格接受此类疗法的把关人。智障成人在生物标志物研究中的代表性不足,将导致他们被排除在疾病改变疗法的治疗范围之外,从而使这一群体已经面临的医疗保健不公平现象永久化。本系列论文旨在总结目前在智障(非唐氏综合症所致)和疑似认知能力下降人群中应用阿尔茨海默病生物标志物的证据。
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来源期刊
Lancet Healthy Longevity
Lancet Healthy Longevity GERIATRICS & GERONTOLOGY-
CiteScore
16.30
自引率
2.30%
发文量
192
审稿时长
12 weeks
期刊介绍: The Lancet Healthy Longevity, a gold open-access journal, focuses on clinically-relevant longevity and healthy aging research. It covers early-stage clinical research on aging mechanisms, epidemiological studies, and societal research on changing populations. The journal includes clinical trials across disciplines, particularly in gerontology and age-specific clinical guidelines. In line with the Lancet family tradition, it advocates for the rights of all to healthy lives, emphasizing original research likely to impact clinical practice or thinking. Clinical and policy reviews also contribute to shaping the discourse in this rapidly growing discipline.
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