Bone is living mineralized tissue, constantly remodeled by osteoblasts (building) and osteoclasts (resorbing) under mechanical load and hormonal control. Collagen forms about 30% of bone mass, with calcium and other minerals making up most of the rest.

Thyroid drives renewal, not just resorption

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Ray Peat argued that adequate thyroid hormone supports bone renewal, and that the bone-breakdown markers that rise with active thyroid function reflect healthy turnover rather than pathological loss:[1]

T3 increases the formation of bone.

The thyroid hormone supports bone renewal, and increases indicators of bone breakdown in the blood.

Calcium itself has effects beyond structural mineral supply: Peat described it as lowering the same stress-adjacent signals (adrenaline, parathyroid hormone, prolactin) that drive bone loss:

Calcium activates mitochondrial respiration, and lowers adrenaline, parathyroid hormone, and prolactin.

Vitamin K2 specifically stimulates production of osteocalcin and osteonectin, two of the key non-collagen bone proteins, while progesterone and estrogen act oppositely on the carbonic-anhydrase pathway involved in bone remodeling.[1]

Practice

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Calcium, vitamin K2, vitamin D, adequate protein, and progesterone/estrogen balance all matter; weight-bearing movement helps when the body is adequately fueled to use it.

See also

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References

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