Association of blood-based neurodegenerative biomarkers with cognitive functioning and dementia in India (LASI-DAD) and the United States (HRS) - Scorecard - MDSpire

Association of blood-based neurodegenerative biomarkers with cognitive functioning and dementia in India (LASI-DAD) and the United States (HRS)

  • By

  • Jung Ki Kim

  • Masroor Anwar

  • Abhishek Gupta

  • Bharat Thyagarajan

  • Peifeng Hu

  • Jessica D Faul

  • David R Weir

  • Kenneth M Langa

  • Jinkook Lee

  • Sharmistha Dey

  • Eileen M Crimmins

  • August 21, 2025

  • 0 min

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Clinical Scorecard: Linking Blood Neurodegenerative Biomarkers to Cognitive Abilities and Dementia in Older Adults: Insights from India (LASI-DAD) and the United States (HRS)

At a Glance

CategoryDetail
ConditionCognitive decline and dementia
Key MechanismsBlood-based neurodegenerative biomarkers including Aβ42/Aβ40 ratio, GFAP, NfL, and pTau181 reflecting amyloid pathology, astrocytic activation, axonal damage, and tau pathology
Target PopulationOlder adults in India and the United States
Care SettingPopulation-based epidemiological and clinical research settings; potential for clinical screening and monitoring

Key Highlights

  • Higher GFAP and NfL levels are associated with worse cognitive function and increased dementia risk in both Indian and US older adults.
  • The Aβ42/Aβ40 ratio shows divergent associations: higher ratio linked to worse cognition and dementia in US, but better cognition in Indian population.
  • pTau181 generally shows no significant association with cognitive functioning in either country.

Guideline-Based Recommendations

Diagnosis

  • Utilize blood-based biomarkers (Aβ42/Aβ40 ratio, GFAP, NfL) as practical tools for early detection of cognitive impairment and dementia.
  • Consider cross-national differences in biomarker associations when interpreting results.

Management

  • Incorporate blood biomarker testing to monitor neurodegenerative progression and potentially guide treatment decisions.
  • Use blood-based biomarkers to complement existing diagnostic modalities, reducing reliance on costly PET scans and CSF analysis.

Monitoring & Follow-up

  • Regularly assess GFAP and NfL levels to track cognitive decline and dementia progression, especially in US populations.
  • Recognize that biomarker trajectories may differ by population; monitor accordingly.

Risks

  • Interpret biomarker levels cautiously due to potential variability influenced by environmental, social, and economic factors.
  • Avoid overreliance on pTau181 alone given its limited association with cognitive outcomes in studied populations.

Patient & Prescribing Data

Older adults from diverse socio-economic and environmental backgrounds in India and the United States

Blood-based neurodegenerative biomarkers offer a less invasive, cost-effective method for early detection and monitoring of dementia, facilitating timely intervention and potentially improving outcomes.

Clinical Best Practices

  • Employ validated, sensitive blood assays for neurodegenerative biomarkers to ensure reliable cross-population comparisons.
  • Integrate biomarker data with clinical and cognitive assessments for comprehensive evaluation.
  • Consider environmental and socio-cultural factors that may modify biomarker-cognition relationships when applying findings clinically.

References

Original Source(s)

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