GLP-1 receptor agonist (public encyclopedia provenance reconstruction)
Reconstructed from 22 public encyclopedia revisions showing article evolution
22 revisions 3 claim families 14 variants 9 events
Independent assertion extraction and claim-family grouping by two analysts, with disagreements resolved by documented criteria.
Documented disagreement
Disagreement: Bridge process split a drug-list assertion into two families because word overlap fell below the 0.5 threshold; human analyst treated it as one semantic family.
Resolution: Added section-anchored joining: merge assertions in the same section when overlap > 0.3.
Evidence movement detected relative to stated reliance. Review when practical.
- Evidence trajectory is moderate based on 3 claim families and 3 assessments.
- Reliance scope is strong from 1 endorsement(s) and 2 operational-use commitment(s).
- Feasibility signals are strong from assertion scan for restrictions and approvals.
| Family | Direction | Variants | Disputes | Last change | Basis |
|---|---|---|---|---|---|
| fam-sentence-1 | disputed | 3 | 1 | 2012-08-22 | analyst asserted |
| fam-sentence-2 | mixed | 7 | 0 | 2012-09-27 | analyst asserted |
| fam-sentence-3 | mixed | 4 | 0 | 2012-09-27 | analyst asserted |
One of their advantages is that they have a lower risk of ca...
Relationships
Licenced : exenatide (2005) Under investigation : liragluti...
Relationships
Glucagon-like peptide-1 agonists (GLP-1 agonists) are new cl...
Relationships
Reverted edits by [[Special:Contributions/59.95.72.254|59.95.72.254]] ([[User talk:59.95.72.254|talk]]) to last revision by PhiLiP ([[WP:HG|HG]])
FDA approval provides direct institutional operationalization of the class-level T2D claim.
Add liraglutide to the list of licensed GLP-1 agonists without changing the family scope.
Endorsement supports the class claim but is inferred from guideline language, not an operational record; retain with ASCVD qualification.
FDA approval converts the evidence claim "GLP-1 agonists are a class of drugs for type 2 diabetes" into an operational regulatory commitment for exenatide.
FDA approval extends the operational commitment to another GLP-1 agonist, supporting the family that exenatide and liraglutide are licensed options.
ADA Standards of Care endorse GLP-1 receptor agonists for type 2 diabetes, particularly when atherosclerotic cardiovascular disease is present. This is an endorsement inferred from guideline language, not an operational record of a specific institution acting on it.
Changes in related specimens can affect this claim history. These links are the seed of monitoring: they show where an event in one domain should trigger reconsideration in another.
FDA approval of liraglutide for chronic weight management strengthens the cross-specimen claim that GLP-1-class drugs, including liraglutide, have an obesity/weight-management indication.
The GLP-1 class ADA endorsement supports the liraglutide T2D mechanism claim because liraglutide is a member of the endorsed class.
This public example shows a capability NextConsensus can deploy now: reconstructing how a medical claim changed across source versions, grouping related statements into claim families, surfacing where the record was disputed or weakened, linking claims to evidence of institutional reliance, and propagating impacts across related specimens.
The underlying method preserves source-addressable artifacts, extracted assertions, claim identity, reviewer-attributed state, reliance inferences, and cross-specimen impact links. The specimen is illustrative; it is not a recommendation for clinical or institutional action.
Evidentiary
- public encyclopedia version identifiers
- Edit timestamps
- Editor usernames
- Edit comments
- Citation URLs
- Page move records
- Template changes
Derived
- Sentence-level diffs (before/after)
- Citation added/removed events
- Section reorganization events
- Edit magnitude (minor/moderate/major)
- Content change type
- Key terms extraction
- Direction signal (strengthening/weakening/neutral)
Inferred
- Claim family membership
- Claim variant relationships
- Confidence assignment
- Impact direction
- Decision rationale reconstruction
- Reliance commitment interpretation