4.7 Article

β-Amyloid, Tau, Neurodegeneration Classification and Eligibility for Anti-amyloid Treatment in a Memory Clinic Population

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NEUROLOGY
卷 99, 期 19, 页码 E2102-E2113

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/WNL.0000000000201043

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资金

  1. Karolinska Institutet [6057695]
  2. Janssen Pharmaceutica NV [6057695]
  3. EU Joint Programme-Neurodegenerative Disease Research (JPND) EURO-FINGERS grant
  4. Alzheimerfonden (Sweden)
  5. Swedish Research Council
  6. Region Stockholm (ALF, Sweden)
  7. Center for Innovative Medicine (CIMED) at Karolinska Institute (Sweden)
  8. Stiftelsen Stockholms sjukhem (Sweden)
  9. Knut and Alice Wallenberg Foundation (Sweden)
  10. Konung Gustaf V:s och Drottning Victorias Frimurarstiftelse (Sweden)
  11. EU/EFPIA Innovative Medicines Initiative Joint Undertaking EPAD grant
  12. European Research Council [804371]
  13. Academy of Finland [317465]
  14. European Research Council (ERC) [804371] Funding Source: European Research Council (ERC)
  15. Academy of Finland (AKA) [317465, 317465] Funding Source: Academy of Finland (AKA)

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This study conducted in a memory clinic in Sweden applied the ATN system to assess patient eligibility for anti-amyloid treatment, showing that the majority of patients did not meet the criteria and emphasizing the need for continued development of disease-modifying treatments with different mechanisms.
Background and Objectives ATN (beta-amyloid [A beta], tau, neurodegeneration) system categorizes individuals based on their core Alzheimer disease (AD) biomarkers. An important potential future use for ATN is therapeutic decision-making in clinical practice once disease-modifying treatments (e.g., antiamyloid), become widely available. In this cross-sectional study, we applied ATN and estimated potential eligibility for anti-amyloid treatment in a real-life memory clinic with biomarker assessments integrated into the routine diagnostic procedure and all specialized resources available for the implementation of novel treatments. Methods We included all consecutive patients at the Karolinska University Hospital Memory clinic in Solna, Stockholm, Sweden, who had their first diagnostic visit in April 2018-February 2021, informed consent for the clinic research database, and available clinical and biomarker (CSF and imaging) data. ATN classification was based on CSF A beta 42 (or A beta 42/40; A), CSF phosphorylated tau (T), and medial temporal lobe atrophy (N). For CSF markers, we applied laboratory cutoffs and data-driven cutoffs for comparison (determined with Gaussian mixture modeling). Eligibility for anti-amyloid treatment was assessed following the published recommendations for aducanumab (AD dementia or mild cognitive impairment [MCI] with no evidence of non-AD etiology, appropriate level of cognition, and AD-consistent CSF profile). Results The study population consisted of 410 patients (52% subjective cognitive impairment, 23% MCI, and 25% any dementia; age 59 +/- 7 years, 56% women). Regardless of biomarker cutoffs, most patients were A-T-N- (54%-57%). A+ prevalence was 17%-30% (higher with data-driven cutoffs). Up to 13% of all patients (27% of those with MCI and 28% of those with dementia) were potentially eligible for anti-amyloid treatment when AD-consistent CSF was defined as any A+ profile. When A+T+ profile was required, treatment was targeted more to the dementia than MCI stage (eligibility up to 14% in MCI and 22% in dementia). The opposite applied to earlier-stage intervention (A+T-N-; eligibility up to 12% in MCI and 2% in dementia). Discussion In a memory clinic setting with all necessary infrastructure and national guidelines in place for dementia diagnostic examination (best-case scenario), most of the patients did not meet the eligibility criteria for anti-amyloid treatment. Continuing the development of disease-modifying treatments with different mechanisms of action is a priority.

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