A multi-center blinded prospective study of urine neural thread protein measurements in patients with suspected Alzheimer's disease

被引:53
作者
Goodman, Ira
Golden, Greg
Flitman, Stephen
Xie, Kevin
McConville, Matthew
Levy, Susanna
Zimmerman, Earl
Lebedeva, Zinaida
Richter, Ralph
Minagar, Alireza
Averback, Paul
机构
[1] Orlando Reg Healthcare Syst, Dept Neurol, Orlando, FL 32801 USA
[2] Thomas Jefferson Univ, Sch Med, VA Med Ctr, Coatesville, PA USA
[3] 21st Century Neurol, Phoenix, AZ USA
[4] Ctr Care Clin, St Cloud, MN USA
[5] Nymox Corp, Hasbrouck Hts, NJ USA
[6] Mt Sinai Sch Med, Elmhurst Hosp, Elmhurst, NY USA
[7] Albany Med Coll, Albany, NY 12208 USA
[8] Univ Hosp Hlth Care Syst, Beachwood, OH USA
[9] Univ Oklahoma, Tulsa, OK USA
[10] Louisiana State Univ, Hlth Sci Ctr, Dept Neurol, Shreveport, LA 71105 USA
关键词
D O I
10.1016/j.jamda.2006.07.002
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
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 mu g/mL). There were 90.7% of subjects diagnosed as definite non-AD who had a normal NTP measurement (<= 22 mu g/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.
引用
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页码:21 / 30
页数:10
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