4.7 Article

Prevalence of Amyloid PET Positivity in Dementia Syndromes A Meta-analysis

期刊

JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
卷 313, 期 19, 页码 1939-1949

出版社

AMER MEDICAL ASSOC
DOI: 10.1001/jama.2015.4669

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资金

  1. National Institute on Aging [U01 AG016976, P50 AG005681, P01 AD 003991, P01 AD 026276]
  2. National Institute on Aging, the National Institute of Biomedical Imaging and Bioengineering [U01 AG024904]
  3. Canadian Institutes of Health Research
  4. Australian Commonwealth Scientific Industrial and Research Organization [CSIRO]
  5. Edith Cowan University [ECU]
  6. Mental Health Research Institute [MHRI]
  7. Alzheimer's Australia [AA]
  8. National Ageing Research Institute [NARI]
  9. Austin Health
  10. CogState
  11. Hollywood Private Hospital
  12. Sir Charles Gardner Hospital
  13. National Health and Medical Research Council (NHMRC)
  14. Dementia Collaborative Research Centres program (DCRC2)
  15. Science and Industry Endowment Fund (SIEF)
  16. Innovative Medicines Initiative Joint Undertaking under EMIF [115372]
  17. European Union
  18. German research foundation (Deutsche Forschungsgemeinschaft) [HE 4560/1-2, DR 445/3-1, DR 445/4-1]
  19. KKF-grant for clinical research of the Technische Universitat Munchen
  20. Health and Health Services Research Fund [06070231]
  21. Lui Che Woo Institute of Innovative Medicine
  22. Fred Simmons and Olga Mohan, and the Joanne Knight Alzheimer's Research Initiative of the Washington Knight Alzheimer's Disease Research Center
  23. French Ministry of Health [PHRC-N 2008 1004]
  24. EC-FP6-project (DiMI) [LSHB-CT-2005-512146]
  25. Pennsylvanian Department of Health [4100037703]
  26. NIH NCRR [UL1RR024992]
  27. NIH NINDS [NS075321]
  28. American Parkinson Disease Association (APDA) Advanced Research Center for Parkinson Disease at Washington University in St. Louis
  29. Greater St Louis Chapter of the APDA
  30. Center for Translational Molecular Medicine (CTMM), project LeARN [02N-101]
  31. Agence Nationale de la Reserche
  32. Programme Hospitalier de Reserche Clinique
  33. Region Basse Normandie
  34. Institut National de la Sante et de la Reserche Medicale (INSERM)

向作者/读者索取更多资源

IMPORTANCE Amyloid-beta positron emission tomography (PET) imaging allows in vivo detection of fibrillar plaques, a core neuropathological feature of Alzheimer disease (AD). Its diagnostic utility is still unclear because amyloid plaques also occur in patients with non-AD dementia. OBJECTIVE To use individual participant data meta-analysis to estimate the prevalence of amyloid positivity on PET in a wide variety of dementia syndromes. DATA SOURCES The MEDLINE and Web of Science databases were searched from January 2004 to April 2015 for amyloid PET studies. STUDY SELECTION Case reports and studies on neurological or psychiatric diseases other than dementia were excluded. Corresponding authors of eligible cohorts were invited to provide individual participant data. DATA EXTRACTION AND SYNTHESIS Data were provided for 1359 participants with clinically diagnosed AD and 538 participants with non-AD dementia. The reference groups were 1849 healthy control participants (based on amyloid PET) and an independent sample of 1369 AD participants (based on autopsy). MAIN OUTCOMES AND MEASURES Estimated prevalence of positive amyloid PET scans according to diagnosis, age, and apolipoprotein E (APOE) epsilon 4 status, using the generalized estimating equations method. RESULTS The likelihood of amyloid positivity was associated with age and APOE epsilon 4 status. InAD dementia, the prevalence of amyloid positivity decreased from age 50 to 90 years in APOE epsilon 4 noncarriers(86%[95% CI, 73%-94%] at 50 years to68%[95% CI, 57%-77%] at 90 years; n = 377) and to a lesser degree in APOE epsilon 4 carriers (97%[95% CI, 92%-99%] at 50 years to 90%[95% CI, 83%-94%] at 90 years; n = 593; P <.01). Similar associations of age and APOE epsilon 4 with amyloid positivity were observed in participants with AD dementia at autopsy. Inmost non-AD dementias, amyloid positivity increased with both age (from 60 to 80years) and APOE epsilon 4 carriership. [GRAPHICS] CONCLUSIONS AND RELEVANCE Among participants with dementia, the prevalence of amyloid positivity was associated with clinical diagnosis, age, and APOE genotype. These findings indicate the potential clinical utility of amyloid imaging for differential diagnosis in early-onset dementia and to support the clinical diagnosis of participants with AD dementia and noncarrier APOE epsilon 4 status who are older than 70 years.

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