KLEORB
tested at a psychologists center (130IQ)..
- Joined
- Oct 15, 2023
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before we start this. many who are interested in romosozumab might not know the actual study review of what is does and what its for.
so officiously a powerful monoclonal antibody treatment for severe osteoporosis in postmenopausal women at high fracture risk, working by stimulating bone formation anabolic and reducing bone breakdown (anti-resorptive) for 12 monthly injections, often followed by standard therapy to maintain gains. It carries a black box warning for increased risk of heart attack, stroke, and cardiovascular death, AND should NOT! be used if a patient has had an MI or stroke in the past year, with common side effects including joint pain, headaches, and injection site reactions
Don't believe me?
read this:
https://investors.amgen.com/news-releases/news-release-details/results-phase-3-frame-study-romosozumab-showed-significant?utm_source
now lets look at the charts shall we
Keep in mind this is without denosumab.
OVERALL??:
Short 6-month course:
look at the chance % spike up WITH deno. NOT MIRIN!, your chances of getting strokes and heart attacks even without recent reports of MI, TIA, ETC+ spikes up to overall 90%-100+% that's a whole 55-70+% increase. THATS ALOT.
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what's personally better? just taking romo itself for 6 months. statistics are very obtuse.
If i get new reviews and report for this topic im willingly to update this thread
i will be doing more reports and reviews with alendronate and Bisphosphonate.
have a blessed day.
so officiously a powerful monoclonal antibody treatment for severe osteoporosis in postmenopausal women at high fracture risk, working by stimulating bone formation anabolic and reducing bone breakdown (anti-resorptive) for 12 monthly injections, often followed by standard therapy to maintain gains. It carries a black box warning for increased risk of heart attack, stroke, and cardiovascular death, AND should NOT! be used if a patient has had an MI or stroke in the past year, with common side effects including joint pain, headaches, and injection site reactions
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Mechanism of Potential Cardiovascular Risk
- Sclerostin and Wnt signaling in blood vessels
- Sclerostin isn’t only in bone—it’s expressed in vascular tissue (like arteries).
- Sclerostin normally acts as a brake on Wnt signaling, which can limit vascular calcification.
- Blocking sclerostin with romosozumab may remove that brake, potentially promoting arterial stiffness or plaque calcification in some patients.
- Endothelial function
- Wnt signaling influences endothelial cells and in which line blood vessels.
- Excess Wnt activity might impair normal endothelial regulation, slightly increasing risk of hypertension or thrombotic events.
- Inflammation vascular remodeling
- Some preclinical studies suggest altered Wnt activity could promote pro-inflammatory signaling in vessels, which is associated with atherosclerosis progression.
Don't believe me?
read this:
https://investors.amgen.com/news-releases/news-release-details/results-phase-3-frame-study-romosozumab-showed-significant?utm_source
now lets look at the charts shall we
| Metric | 6-Month Course | 12-Month Course | Notes |
|---|---|---|---|
| Spine BMD gain (% of 12-month max) | 70–75% | 100% | Spine responds fastest; most early anabolic activity |
| Hip/femoral neck BMD gain (% of 12-month max) | 50–60% | 100% | Hip/appendicular bones grow slower; partial gain at 6 months |
| Total body/new bone formation (% of 12-month max) | 60–65% | 100% | Weighted average across axial + appendicular skeleton |
| Facial/cranial bone formation (% of 12-month max) | ~50–60% | 100% | Extrapolated from appendicular skeleton data; less robust than spine |
| Fracture risk reduction (% relative to placebo) | ~40–50% | ~70–80% | Partial but meaningful at 6 months; full protection by 12 months |
| Cumulative cardiovascular risk (heart attack / stroke) | 30–40% of 12-mo risk | 100% | Shorter course reduces exposure to systemic Wnt overactivation |
| Off-target calcification / soft tissue Wnt effects | 20–30% of 12-mo risk | 100% | Early months mostly safe; risk accumulates with duration |
| Success rate of anabolic bone formation without major negative effect | ~60–65% | ~50–55% | Combines efficacy and risk: shorter course safer but partially effective; full course maximizes gains but increases risk |
OVERALL??:
Short 6-month course:
- Good early gains, especially in spine.
- Meaningful fracture protection.
- Safer overall; lower off-target risk.
- Partial skeletal benefit—hip and total body may need follow-up.
- Full 12-month course:
- Maximum BMD gains across all regions.
- Full fracture risk reduction.
- Higher cumulative risk of cardiovascular events or soft tissue effects.
- Success rate slightly lower due to risk trade-offs.
| Metric / Outcome | 6-Month Romosozumab | 12-Month Romosozumab | Romosozumab + Denosumab | Notes |
|---|---|---|---|---|
| Spine BMD gain (% of 12-mo max) | 70–75% | 100% | 100–110% | Denosumab locks gains, small incremental spine increase |
| Hip/femoral neck BMD gain (% of 12-mo max) | 50–60% | 100% | 100–105% | Denosumab improves slower hip gains |
| Total body/new bone formation (% of 12-mo max) | 60–65% | 100% | 100–110% | Skeleton-wide support with denosumab |
| Fracture risk reduction (% relative to placebo) | ~40–50% | ~70–80% | ~80–85% | Denosumab adds protection, especially at hip |
| Success rate of anabolic maintenance | ~60–65% | ~50–55% | ~80–85% | Combines efficacy and risk profile |
| Cumulative cardiovascular risk (MI/stroke) | 30–40% of 12-mo risk | 100% | ~90–100% | Short course reduces exposure; denosumab doesn’t add cardiac risk significantly, but long romo exposure contributions |
| Off-target calcification / soft tissue Wnt effects | 20–30% of 12-mo risk | 100% | ~90–95% | Denosumab does not worsen Wnt-related calcification; main risk is romo duration |
| Overall safety balance | Higher (less cumulative risk) | Moderate (max anabolic gain but higher cumulative risk) | High (maintains gains; cardiovascular risk primarily from prior romo exposure) | Denosumab preserves bone without adding major off-target risks |
| Strategy | Bone Gain | Risk Exposure | Overall |
|---|---|---|---|
| 6-mo romo | Rapid but partial | Low | Safer early benefit |
| 12-mo romo | Maximal | High | Best skeletal gain but higher systemic risk |
| Romo + denosumab | Maximal + incremental | Moderate-High (risk mostly from romo) | Best balance: sustain gains, improve fracture protection, minimal extra systemic risk |
what's personally better? just taking romo itself for 6 months. statistics are very obtuse.
If i get new reviews and report for this topic im willingly to update this thread
i will be doing more reports and reviews with alendronate and Bisphosphonate.
have a blessed day.