Table 2.
Cardiovascular risk in spaceflight, cardiovascular risk in spaceflight and epidemiological evidence for radiation-induced cardiovascular risk
| Level of evidence | Source/Model | Key cardiovascular observations | Role in risk assessment |
|---|---|---|---|
| Epidemiologic | Human: LSS (atomic bomb) and radiotherapy | Dose-dependent increase in ischemic heart disease and stroke (>0.5 Gy). | Establishes the primary terrestrial baseline for human risk. |
| Clinical | Human: ISS and Apollo Crews | Carotid-intima thickness shifts; microvascular remodeling in LEO. | Validates human physiological response in the space environment. |
| Mechanistic | Animal: simGCRsim Murine models | Accelerated atherosclerosis; myocardial fibrosis; reduced EF%. | Recapitulates the deep space (High-LET) hazard profile. |
| Molecular | Experimental: Omics and in vitro | RNA dysregulation; cytokine signaling; oxidative stress. | Identifies predictive biomarkers and early-warning signatures. |
| Epidemiological evidence for radiation-induced cardiovascular risk | |||
| Cohort type | Key examples | Exposure characteristics | Relevance to spaceflight |
|
Atomic bomb survivors |
Life Span Study (LSS) | Acute, high-dose-rate; mixed photon-neutron field. | Foundational for stochastic risk and dose–response modeling. |
|
Clinical radiotherapy |
Breast cancer and Hodgkin lymphoma survivors | High-dose, localized fractions; primarily photons. | Identifies specific tissue reactions (valvular disease, pericarditis). |
| Occupational | INWORKS, Mayak workers, Chornobyl liquidators | Chronic, low-dose-rate; protracted over years; primarily gamma/neutron. | Most relevant for modeling the cardiovascular effects of protracted GCR exposure. |
This table summarizes the hierarchy of evidence characterizing the cardiovascular hazards associated with space travel and epidemiological evidence for radiation-induced cardiovascular risk, both categorized by research scale and clinical relevance.