Baseline features of the AMYPAD Diagnostic and Patient Management Study (DPMS) participants: Neuroimaging / differential diagnosis. (7th December 2020)
- Record Type:
- Journal Article
- Title:
- Baseline features of the AMYPAD Diagnostic and Patient Management Study (DPMS) participants: Neuroimaging / differential diagnosis. (7th December 2020)
- Main Title:
- Baseline features of the AMYPAD Diagnostic and Patient Management Study (DPMS) participants
- Authors:
- Altomare, Daniele
Collij, Lyduine
Garibotto, Valentina
Poitrine, Léa
Moro, Christian
Alves, Isadora Lopes
van Maurik, Ingrid S.
Berkhof, Johannes
Scheltens, Philip
Delrieu, Julien
Molinuevo, Jose Luis
Nordberg, Agneta K
Jessen, Frank
Walker, Zuzana
Démonet, Jean‐François
Gismondi, Rossella
Farrar, Gill
Barkhof, Frederik
Stephens, Andrew W
Frisoni, Giovanni B - Abstract:
- Abstract: Background: AMYPAD‐DPMS is the largest European, multicenter, prospective and randomized study assessing clinical utility and cost‐effectiveness of amyloid‐PET in a controlled but realistic clinical setting. In the present abstract we report preliminary results on the baseline features of the first study participants. Method: A total of 900 participants (300 with subjective cognitive decline plus [SCD+], 300 with mild cognitive impairment [MCI], and 300 with dementia) will be enrolled and randomized into 3 study arms: ARM‐1, amyloid‐PET performed early in the diagnostic workup; ARM‐2, amyloid‐PET performed late in the diagnostic work‐up; and ARM‐3, amyloid‐PET performed if and when the physician chooses to. Result: As of January 23 rd 2020, 617 participants (154 SCD+, 303 MCI, and 160 dementia) have been enrolled from 8 centers. Baseline features are reported in Table 1. SCD+ participants are younger than MCI ( p =0.006) and dementia ( p <0.001) participants. SCD+ are more highly educated than MCI and dementia ( p <0.001), and MCI are more highly educated that dementia ( p =0.008). As expected, worse global cognition is observed in dementia ( p <0.001) compared to MCI and SCD+, and in MCI compared to SCD+ ( p <0.001). Among those who already underwent amyloid‐PET, 34% (30/88) of SCD+, 58% (90/155) of MCI, and 74% (60/81) of dementia patients were amyloid‐positive based on visual PET scan assessment. Conclusion: The socio‐demographic and cognitive features of theAbstract: Background: AMYPAD‐DPMS is the largest European, multicenter, prospective and randomized study assessing clinical utility and cost‐effectiveness of amyloid‐PET in a controlled but realistic clinical setting. In the present abstract we report preliminary results on the baseline features of the first study participants. Method: A total of 900 participants (300 with subjective cognitive decline plus [SCD+], 300 with mild cognitive impairment [MCI], and 300 with dementia) will be enrolled and randomized into 3 study arms: ARM‐1, amyloid‐PET performed early in the diagnostic workup; ARM‐2, amyloid‐PET performed late in the diagnostic work‐up; and ARM‐3, amyloid‐PET performed if and when the physician chooses to. Result: As of January 23 rd 2020, 617 participants (154 SCD+, 303 MCI, and 160 dementia) have been enrolled from 8 centers. Baseline features are reported in Table 1. SCD+ participants are younger than MCI ( p =0.006) and dementia ( p <0.001) participants. SCD+ are more highly educated than MCI and dementia ( p <0.001), and MCI are more highly educated that dementia ( p =0.008). As expected, worse global cognition is observed in dementia ( p <0.001) compared to MCI and SCD+, and in MCI compared to SCD+ ( p <0.001). Among those who already underwent amyloid‐PET, 34% (30/88) of SCD+, 58% (90/155) of MCI, and 74% (60/81) of dementia patients were amyloid‐positive based on visual PET scan assessment. Conclusion: The socio‐demographic and cognitive features of the first 68% of AMYPAD‐DPMS participants are as expected for a memory clinic population, confirming the inclusion/exclusion criteria resulted in a representative sample. These results support the generalizability of the final study results. The end of participants' enrolment is expected by mid‐2020. … (more)
- Is Part Of:
- Alzheimer's & dementia. Volume 16(2020)Supplement 5
- Journal:
- Alzheimer's & dementia
- Issue:
- Volume 16(2020)Supplement 5
- Issue Display:
- Volume 16, Issue 5 (2020)
- Year:
- 2020
- Volume:
- 16
- Issue:
- 5
- Issue Sort Value:
- 2020-0016-0005-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2020-12-07
- Subjects:
- Alzheimer's disease -- Periodicals
Alzheimer Disease -- Periodicals
Dementia -- Periodicals
Démence
Maladie d'Alzheimer
Périodique électronique (Descripteur de forme)
Ressource Internet (Descripteur de forme)
616.83 - Journal URLs:
- http://www.sciencedirect.com/science/journal/15525260 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1002/alz.042628 ↗
- Languages:
- English
- ISSNs:
- 1552-5260
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library DSC - 0806.255333
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