» Articles » PMID: 33632704

Effect of Reductions in Amyloid Levels on Cognitive Change in Randomized Trials: Instrumental Variable Meta-analysis

Abstract

Objective: To evaluate trials of drugs that target amyloid to determine whether reductions in amyloid levels are likely to improve cognition.

Design: Instrumental variable meta-analysis.

Setting: 14 randomized controlled trials of drugs for the prevention or treatment of Alzheimer's disease that targeted an amyloid mechanism, identified from ClinicalTrials.gov.

Population: Adults enrolled in randomized controlled trials of amyloid targeting drugs. Inclusion criteria for trials vary, but typically include adults aged 50 years or older with a diagnosis of mild cognitive impairment or Alzheimer's disease, and amyloid positivity at baseline.

Main Outcome Measures: Analyses included trials for which information could be obtained on both change in brain amyloid levels measured with amyloid positron emission tomography and change in at least one cognitive test score reported for each randomization arm.

Results: Pooled results from the 14 randomized controlled trials were more precise than estimates from any single trial. The pooled estimate for the effect of reducing amyloid levels by 0.1 standardized uptake value ratio units was an improvement in the mini-mental state examination score of 0.03 (95% confidence interval -0.06 to 0.1) points. This study provides a web application that allows for the re-estimation of the results when new data become available and illustrates the magnitude of the new evidence that would be necessary to achieve a pooled estimate supporting the benefit of reducing amyloid levels.

Conclusions: Pooled evidence from available trials reporting both reduction in amyloid levels and change in cognition suggests that amyloid reduction strategies do not substantially improve cognition.

Citing Articles

Clusterin induced by OPC phagocytosis blocks IL-9 secretion to inhibit myelination in a model of Alzheimer's disease.

Beiter R, Raghavan T, Suchocki O, Ennerfelt H, Rivet-Noor C, Merchak A Heliyon. 2025; 11(1):e41635.

PMID: 39866464 PMC: 11761289. DOI: 10.1016/j.heliyon.2025.e41635.


Serum metabolome profiling in patients with mild cognitive impairment reveals sex differences in lipid metabolism.

Escarcega R, Vijay Kumar M, Kyriakopoulos V, Ortiz G, Gusdon A, Fan H bioRxiv. 2024; .

PMID: 39605322 PMC: 11601308. DOI: 10.1101/2024.11.11.623108.


Assessing clinical progression measures in Alzheimer's disease trials: A systematic review and meta-analysis.

McLaughlin J, Scotton W, Ryan N, Hardy J, Shoai M Alzheimers Dement. 2024; 20(12):8673-8683.

PMID: 39439251 PMC: 11667530. DOI: 10.1002/alz.14314.


Reading and conducting instrumental variable studies: guide, glossary, and checklist.

Walker V, Sanderson E, Levin M, Damraurer S, Feeney T, Davies N BMJ. 2024; 387:e078093.

PMID: 39401839 PMC: 11472180. DOI: 10.1136/bmj-2023-078093.


What's in It for Me? Contextualizing the Potential Clinical Impacts of Lecanemab, Donanemab, and Other Anti-β-amyloid Monoclonal Antibodies in Early Alzheimer's Disease.

Jin M, Noble J eNeuro. 2024; 11(9).

PMID: 39332901 PMC: 11439562. DOI: 10.1523/ENEURO.0088-24.2024.


References
1.
Logovinsky V, Satlin A, Lai R, Swanson C, Kaplow J, Osswald G . Safety and tolerability of BAN2401--a clinical study in Alzheimer's disease with a protofibril selective Aβ antibody. Alzheimers Res Ther. 2016; 8(1):14. PMC: 4822297. DOI: 10.1186/s13195-016-0181-2. View

2.
Cummings J, Ritter A, Zhong K . Clinical Trials for Disease-Modifying Therapies in Alzheimer's Disease: A Primer, Lessons Learned, and a Blueprint for the Future. J Alzheimers Dis. 2018; 64(s1):S3-S22. PMC: 6004914. DOI: 10.3233/JAD-179901. View

3.
Imbimbo B, Ottonello S, Frisardi V, Solfrizzi V, Greco A, Seripa D . Solanezumab for the treatment of mild-to-moderate Alzheimer's disease. Expert Rev Clin Immunol. 2012; 8(2):135-49. DOI: 10.1586/eci.11.93. View

4.
Abushouk A, Elmaraezy A, Aglan A, Salama R, Fouda S, Fouda R . Bapineuzumab for mild to moderate Alzheimer's disease: a meta-analysis of randomized controlled trials. BMC Neurol. 2017; 17(1):66. PMC: 5381133. DOI: 10.1186/s12883-017-0850-1. View

5.
Lannfelt L, Moller C, Basun H, Osswald G, Sehlin D, Satlin A . Perspectives on future Alzheimer therapies: amyloid-β protofibrils - a new target for immunotherapy with BAN2401 in Alzheimer's disease. Alzheimers Res Ther. 2014; 6(2):16. PMC: 4054967. DOI: 10.1186/alzrt246. View