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One row per finding: what was tested, which way the result went, and how the study was built. The answer by area, and where the studies disagree, are on the main page.
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Showing 2 of 382 rows for CSF alpha-synuclein seed amplification assay. One row per study per exposure: a study that tested two different things appears twice, once for each.
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| Exposure | Question | Direction | Outcome measured | Design | People | Effect size, as the source reported it | Source |
|---|---|---|---|---|---|---|---|
| CSF alpha-synuclein seed amplification assay Care, carers and services | Treatment |
Mixed
whyDirection is for the test's accuracy against the reference standard; an accuracy result, not a health outcome. Results ranged from 55% to 100% sensitivity and 60% to 100% specificity across four laboratories using different protocols, with only fair agreement between them (kappa 0.246). |
Sensitivity, specificity and cross-laboratory agreement for dementia with Lewy bodies | cross-sectional study | 30 | On average, the 4 laboratories achieved 78.8% sensitivity (minimum 55%, maximum 100%), 77.5% specificity (minimum 60%, maximum 100%), and 78.5% accuracy (minimum 57%, maximum 100%) for discriminating DLB from controls ... A fair agreement of SAA results was obtained across the 4 laboratories (average κ = 0.246) |
Neurology
2026 ✓ Peer-reviewed PMID 41604609 |
| CSF alpha-synuclein seed amplification assay Care, carers and services | Treatment |
Benefit
whyDirection is for the test's accuracy against the reference standard; an accuracy result, not a health outcome. Smell testing followed by CSF seed amplification only in those with reduced smell predicted brain Lewy body pathology with 94% accuracy and cut CSF testing by 43%; in a living cohort it predicted CSF assay status with 79% accuracy. |
Accuracy for autopsy-confirmed Lewy body pathology and reduction in confirmatory CSF testing | cohort study | 1,567 | Among 358 autopsied participants, the two-step workflow predicted brain LBP with high accuracy overall (94%), and within clinical subgroups (clinical parkinsonism=95%; clinical Alzheimer's disease [AD]=94%; clinically unimpaired [CU]=93%). It reduced the need for confirmatory CSF testing by 43% overall (23% clinical parkinsonism; 35% clinical AD; 80% CU). In an independent in vivo cohort (N=1209), the workflow predicted CSF α-syn SAA status with 79% accuracy and reduced CSF testing by 26% |
Nature Communications
2025 ✓ Peer-reviewed PMID 40764485 |