Head‐to‐Head Comparison of Tau and Amyloid Positron Emission Tomography Visual Reads for Differential Diagnosis of Neurodegenerative Disorders: An International, Multicenter Study

Author:

Soleimani‐Meigooni David N.12ORCID,Smith Ruben3,Provost Karine4,Lesman‐Segev Orit H.5ORCID,Allen Isabel Elaine6,Chen Miranda K.1,Cho Hanna7,Edwards Lauren18,Janelidze Shorena3,La Joie Renaud1,Mundada Nidhi1,Ossenkoppele Rik39,Stomrud Erik310,Strandberg Olof3,Strom Amelia111,Boxer Adam L.1,Dage Jeffrey L.12,Gorno‐Tempini Maria Luisa1,Kramer Joel H.1,Miller Bruce L.1,Rojas Julio C.1,Rosen Howard J.1,Lyoo Chul H.7,Hansson Oskar310ORCID,Rabinovici Gil D.113

Affiliation:

1. Memory and Aging Center, Department of Neurology University of California San Francisco CA USA

2. Molecular Biophysics and Integrated Bioimaging Lawrence Berkeley National Laboratory Berkeley CA USA

3. Clinical Memory Research Unit Lund University Lund Sweden

4. Department of Nuclear Medicine University of Montreal Hospital Center Montréal Canada

5. Department of Diagnostic Imaging Sheba Medical Center, Tel Hashomer Ramat Gan Israel

6. Department of Epidemiology and Biostatistics University of California San Francisco CA USA

7. Department of Neurology, Gangnam Severance Hospital Yonsei University College of Medicine Seoul South Korea

8. Clinical Psychology San Diego State University & University of California San Diego CA USA

9. Alzheimer Center Amsterdam, Department of Neurology Amsterdam Neuroscience, Amsterdam UMC Amsterdam the Netherlands

10. Memory Clinic Skåne University Hospital Lund Sweden

11. Health Sciences and Technology Harvard & Massachusetts Institute of Technology Cambridge MA USA

12. Stark Neuroscience Research Institute Indiana University School of Medicine Indianapolis IN USA

13. Department of Radiology and Biomedical Imaging University of California San Francisco CA USA

Abstract

ObjectiveWe compared the accuracy of amyloid and [18F]Flortaucipir (FTP) tau positron emission tomography (PET) visual reads for distinguishing patients with mild cognitive impairment (MCI) or dementia with fluid biomarker support of Alzheimer's disease (AD).MethodsParticipants with FTP‐PET, amyloid‐PET, and diagnosis of dementia‐AD (n = 102), MCI‐AD (n = 41), non‐AD diseases (n = 76), and controls (n = 20) were included. AD status was determined independent of PET by cerebrospinal fluid or plasma biomarkers. The mean age was 66.9 years, and 44.8% were women. Three readers interpreted scans blindly and independently. Amyloid‐PET was classified as positive/negative using tracer‐specific criteria. FTP‐PET was classified as positive with medial temporal lobe (MTL) binding as the minimum uptake indicating AD tau (tau‐MTL+), positive with posterolateral temporal or extratemporal cortical binding in an AD‐like pattern (tau‐CTX+), or negative. The majority of scan interpretations were used to calculate diagnostic accuracy of visual reads in detecting MCI/dementia with fluid biomarker support for AD (MCI/dementia‐AD).ResultsSensitivity of amyloid‐PET for MCI/dementia‐AD was 95.8% (95% confidence interval 91.1–98.4%), which was comparable to tau‐CTX+ 92.3% (86.7–96.1%, p = 0.67) and tau‐MTL+ 97.2% (93.0–99.2%, p = 0.27). Specificity of amyloid‐PET for biomarker‐negative healthy and disease controls was 84.4% (75.5–91.0%), which was like tau‐CTX+ 88.5% (80.4–94.1%, p = 0.34), and trended toward being higher than tau‐MTL+ 75.0% (65.1–83.3%, p = 0.08). Tau‐CTX+ had higher specificity than tau‐MTL+ (p = 0.0002), but sensitivity was lower (p = 0.02), driven by decreased sensitivity for MCI‐AD (80.5% [65.1–91.2] vs. 95.1% [83.5–99.4], p = 0.03).InterpretationAmyloid‐ and tau‐PET visual reads have similar sensitivity/specificity for detecting AD in cognitively impaired patients. Visual tau‐PET interpretations requiring cortical binding outside MTL increase specificity, but lower sensitivity for MCI‐AD. ANN NEUROL 2024;96:476–487

Funder

Vetenskapsrådet

Alzheimer's Association

Knut och Alice Wallenbergs Stiftelse

National Institute on Aging

National Institute of Neurological Disorders and Stroke

Publisher

Wiley

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