BioConst生物常量

Research reference only. BioConst updates and corrects content over time, but it cannot replace clinician-guided diagnosis, treatment, medication, or testing decisions.

Aging biology / loss of homeostasis

Biology runs on set-points. We track the ones that fail with age.

Map the age-related loss of biological repair capacity without making treatment claims.

Bone

Bone conditions, organized by what fails.

A low-friction map of major bone-condition families. Cards link to existing source-backed research until dedicated condition pages are reviewed.

Bone

Bone mass and fracture resistance

Conditions where bone strength, density, quality, or falls make low-trauma fracture more likely.

Hormone and remodeling disorders

Conditions where bone remodeling speed or hormone signals become the central problem.

Mineralization and kidney-mineral control

Conditions where mineral deposition or kidney-mineral hormone control changes the meaning of bone data.

Structural, systemic & secondary

Inherited, developmental, and structural fragility

Conditions where collagen, osteoclast function, mosaic lesions, or skeletal development alter strength.

Tumor, marrow, and systemic bone destruction

Bone involvement from cancer or marrow disease, kept separate from everyday bone-fragility concerns.

Blood supply, infection, and tissue destruction

Conditions where blood flow failure or infection damages living bone tissue.

Brain

Memory and cognition, organized by what fails.

A source-backed map for memory, cognitive aging, MCI, Alzheimer disease, and the factors that can change cognitive function.

Memory and cognitive decline

Alzheimer disease and neurodegeneration

How Alzheimer disease disrupts memory networks, synapses, amyloid, tau, and brain volume over time.

Alzheimer diseaseAlzheimer disease: memory-network failureAlzheimer disease first disrupts memory-related networks such as the entorhinal cortex and hippocampus, then spreads across brain systems.
Hippocampus / entorhinal memory networkBeta-amyloidTauSynaptic plasticityBrain atrophy
Alzheimer disease: treatment boundariesAlzheimer disease: treatment boundariesCurrent anti-amyloid antibodies can slow progression in some early Alzheimer contexts, but they are not a promise to bring lost memory back.
Anti-amyloid antibodiesARIABeta-amyloidCognitive testing
synapse rebuildingCan synapses be rebuilt, and can neurons be backed up?If neurons and network scaffolding remain, some synaptic compensation may be possible; correctness can only be inferred, and neurons cannot be biologically backed up today.
Synapse lossSynaptic plasticityBrain atrophyHippocampus / entorhinal memory networkCognitive testingAlzheimer biomarkersSV2A PET / synaptic density imaging
Alzheimer root causeWhat is the root cause of Alzheimer disease?Synapse loss is close to the memory problem, but Alzheimer disease is not explained by one root cause.
Beta-amyloidTauSynapse lossSynaptic plasticityBrain atrophy
synapse rebuilding AlzheimerIf synaptic connections came back, would that treat Alzheimer disease?Rebuilding the right working memory-network connections would be a core treatment effect, but more synapses alone would not be enough.
Synapse lossSynaptic plasticityHippocampus / entorhinal memory networkBrain atrophyBeta-amyloidTau

Cognitive aging and decline

The boundary between slower recall, mild cognitive impairment, and dementia-level daily-life loss.

Memory systems and forgetting

How experiences become memory, why recall fails, and why forgetting is not one single process.

Heart

Cardiac function, organized by what fails.

A source-backed map for coronary blood supply, pump reserve, rhythm, valve flow, heart muscle, and pressure load.

Blood

Blood function, organized by what fails.

A source-backed map for oxygen carrying, iron context, clotting, bleeding, platelets, marrow production, and blood cancers.

Oxygen carrying and clotting balance

Clotting and bleeding balance

Conditions where blood clots too much, too little, or in the wrong context.

Iron and blood production context

How iron stores, marrow production, and red-cell size change anemia interpretation.

Red cells and oxygen carrying

Conditions where red blood cells or hemoglobin cannot deliver enough oxygen signal.

Liver

Liver function, organized by what fails.

A source-backed map for liver-cell injury, bile flow, fat context, scarring, and synthetic function.

Kidney

Kidney function, organized by what fails.

A source-backed map for filtration, albumin leakage, fluid balance, acute injury, stones, and kidney failure context.

Filtration, albumin, and fluid balance

Fluid, electrolytes, and acid-base context

Conditions where kidney control of water, salts, and blood chemistry affects the clinical picture.

Filtration and waste clearance

Conditions where kidney filtration, creatinine, eGFR, or urea handling becomes central.

Urine protein and glomerular barrier

Conditions where albumin leakage signals kidney barrier damage or microvascular context.

Lung

Lung function, organized by what fails.

A source-backed map for airflow, gas exchange, infection, scarring, sleep breathing, and pulmonary blood-flow context.

Problem

BioConst

BioConst

Aging appears as drifting biological set-points: bone remodeling, lipid regulation, immune repair, follicle cycling, and tissue renewal all become harder to hold. BioConst studies that loss of control as a research problem, not as medical advice.

The work starts with evidence tracking. Each note separates animal work, early human signals, clinical trials, and unsupported claims, with sources attached to every factual data point.

Research discussion only. Not medical advice.

Operating Rule

Receipts before claims.

Every public fact, number, or model baseline is attached to a visible source. Estimates are marked as estimates. Boundaries stay close to the result.

Initial Evidence Tiers4framework to human data
Source Set5linked references
BoundaryNo adviceresearch discussion