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首页> 外文期刊>Journal of the American Medical Directors Association >A multi-center blinded prospective study of urine neural thread protein measurements in patients with suspected Alzheimer's disease.
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A multi-center blinded prospective study of urine neural thread protein measurements in patients with suspected Alzheimer's disease.

机译:对怀疑患有阿尔茨海默氏病的患者进行尿液神经线蛋白测定的多中心盲前瞻性研究。

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摘要

OBJECTIVE: To investigate the utility of a clinical laboratory ELISA format assay that measures neural thread protein (NTP) in urine in the assessment of patients presenting with cognitive symptoms. DESIGN: A prospective blinded multicentered study. SETTING: Eight US specialty clinics for the evaluation of cognitive or memory disorder or dementia, including memory disorder and dementia clinics, neurology clinics, and psychiatry clinics, in 8 states. PARTICIPANTS: Prospectively enrolled consecutive patients who were newly referred to a specialty clinic for assessment of cognitive or memory disorder symptoms or dementia to rule out or rule in Alzheimer's disease (AD). MEASUREMENTS: Participants provided a first morning urine sample for UNTP measurement for testing at a central core laboratory and subsequently went through specialized diagnostic evaluations in accordance with established clinical criteria. Urine NTP measurement was compared to the diagnostic categorization of the patients as probable or possible AD (according to National Institute of Neurological Communicative Disorders and Stroke and the Alzheimer Disease and Related Disorders Association [NINCDS-ADRDA] criteria), mild cognitive impairment (MCI) (according to Quality Standards Subcommittee of the American Academy of Neurology [AAN] criteria) or definite non-AD. Clinical diagnoses were made without reference to UNTP measurement; the testing laboratory was blinded to both patient identity and clinical diagnoses. RESULTS: A total of 168 enrolled and consented patients provided qualifying urine samples and completed specialized diagnostic workups. There were 91.4% of subjects with probable AD, 37.7% of subjects categorized as possible AD, and 48.6% of subjects with MCI who had an elevated NTP measurement (>22 microg/mL). There were 90.7% of subjects diagnosed as definite non-AD who had a normal NTP measurement (< or =22 microg/mL). CONCLUSION: Noninvasive UNTP test results are potentially helpful as part of the workup of dementia for the nonspecialist to help in the decision as to whether referral and/or more detailed investigation is advisable.
机译:目的:探讨测量尿液中神经线蛋白(NTP)的临床实验室ELISA格式测定法在评估表现出认知症状的患者中的实用性。设计:一项前瞻性多盲盲研究。地点:美国的8个专科诊所,用于评估认知或记忆障碍或痴呆症,包括在8个州的记忆障碍和痴呆症诊所,神经病诊所和精神病学诊所。参与者:前瞻性入组的连续患者,这些患者新近被转诊至专科诊所以评估认知或记忆障碍症状或痴呆,以排除或排除阿尔茨海默氏病(AD)。测量:参与者提供了第一天早晨的尿液样本用于UNTP测量,以在中央核心实验室进行测试,随后根据既定的临床标准进行了专门的诊断评估。将尿液NTP的测量值与患者的诊断分类进行比较,将其分类为可能或可能的AD(根据美国国家神经病学,传染性疾病和中风协会以及阿尔茨海默病和相关疾病协会[NINCDS-ADRDA]的标准),轻度认知障碍(MCI) (根据美国神经病学会[AAN]标准的质量标准小组委员会)或明确的非AD。临床诊断时未参考UNTP测量值;测试实验室对患者身份和临床诊断均视而不见。结果:共有168名入组并获得同意的患者提供了合格的尿液样本并完成了专门的诊断检查。 NTP测量值升高(> 22 microg / mL)的受试者中,有91.4%可能患有AD,37.7%的受试者被归为可能的AD,还有48.6%的MCI受试者。有90.7%的诊断为明确的非AD受试者的NTP测量值正常(<或= 22 microg / mL)。结论:作为非痴呆症检查工作的一部分,非侵入性UNTP测试结果可能有助于非专业人士做出决定是否建议转诊和/或更详细的研究。

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