Dilated cardiomyopathy (LMNA) OMIM 115200
In Dilated cardiomyopathy (LMNA, OMIM 115200), the master switch sits on the ↑ UP branch ([F] forced below); the healthy state is the ON well. The forced corrective direction is to raise s toward ON branch (polarity: clear). Classification: — Honest hold (no matched agent). Direction only — no dose, no efficacy magnitude.
The disease maps to an R19 double-well whose corrective lever is read straight off the cusp (barrier 0.6016, γ 1.5513, spinodal 0.7437). The corrective direction is forced [F]; the agent names below are direction-concordant labels at grade [O] (no dose, no efficacy or safety magnitude). This is a research hypothesis offered to experts, not medical advice.
The emergence switch
The switch for Dilated cardiomyopathy is an R19 double-well emerged from the real proximal-promoter DNA of LMNA. Its geometry is fixed by measured stiffness γ (never fitted); the numbers below are read directly off that cusp.
- emergent axis
- ↑ UP [F]
- healthy branch
- ON
- lesion
- LOF_null
- γ (stiffness)
- 1.5513
- barrier
- 0.6016
- spinodal
- 0.7437
- s_on / s_off
- 1.2455 / -1.2455
- fragility
- 0.00
- corrective polarity
- clear
- forced direction
- raise s toward ON branch
Chemistry feasibility (DIRECTION only [O]). small-molecule recrossing of the fold is geometrically harder (barrier 0.6016 at neutral drive; lower barrier = smaller drive to supply). [O] -- no affinity/potency/dose/efficacy asserted.
The derived corrective lever
The cusp forces a corrective direction: raise s toward ON branch. This is the load-bearing output of the framework — it is [F] forced, and it is falsifiable. 2 lever families are derived; the lead is h-restore (drive modulator).
Agents mapped onto the lever
| agent (class) | dir. | status | phase | map |
|---|---|---|---|---|
| p38 MAPK inhibition reducing the maladaptive MAPK signaling drive downstream of the LMNA lamin defect Muchir 2007 J Clin Invest 117:1282 (activation of mapk pathways links lmna mutations); Fatkin 1999 N Engl J Med 341:1715 (missense mutations in the rod domain of) | decrease | investigational | 2 | ◇ in trials |
Evidence & provenance
| element | grade | basis |
|---|---|---|
| R19 switch & cusp geometry (this page) | [V] verified | emerged from measured promoter γ of LMNA; deterministic, 2×sha256 identical |
| corrective direction | [F] forced | forced by the cusp sign; falsifiable (see lever falsifiers) |
| mapped agents / leads | [O] open | direction-concordance only; corpus-pinned (2026-06-21); no dose, no efficacy/safety magnitude |
Reading the agent column. VALIDATION SIGNAL -- the agent is already approved / established standard for this disease, so the direction logic recovered known clinical practice. Not a new claim by this kit. GENUINE HYPOTHESIS -- no approved indication for this disease; the direction match is a direction-only, untested [O] lead. Basis field grades the evidence (investigational here / in a related condition / off-label / speculative).