# The Bone–Brain Axis: Novel Insights into the Bidirectional Crosstalk in Depression and Osteoporosis

**Authors:** Pengpeng Li, Yangyang Gao, Xudong Zhao

PMC · DOI: 10.3390/biom16020213 · Biomolecules · 2026-01-31

## TL;DR

This review explores how depression and osteoporosis are linked through a bidirectional bone-brain communication system, offering new insights into shared causes and potential treatments.

## Contribution

The paper provides a comprehensive overview of molecular pathways linking depression and osteoporosis through the bone–brain axis, highlighting novel therapeutic targets.

## Key findings

- Depression promotes bone loss via HPA axis activation, sympathetic overactivity, and inflammation.
- Bone-derived factors like osteocalcin and lipocalin 2 influence brain function by affecting neurogenesis and serotonin signaling.
- Bidirectional communication between bone and brain is modulated by circadian rhythms and genetic factors.

## Abstract

Depression and osteoporosis frequently co-occur, presenting a significant and increasing clinical challenge, especially among older adults. Growing research highlights the bone–brain axis, a complex bidirectional communication network connecting the skeletal and central nervous systems, as a central mechanism linking these conditions. This review comprehensively examines the current knowledge of the molecular and cellular pathways within this axis that contribute to depression–osteoporosis interactions. It details how depression promotes bone loss through sustained hypothalamic–pituitary–adrenal axis activation, sympathetic nervous system overactivity, and chronic low-grade inflammation. This review also explores how bone-derived factors, including osteocalcin, lipocalin 2, and extracellular vesicles, cross the blood–brain barrier to influence brain function by regulating hippocampal neurogenesis, serotonin signaling, and neuroinflammation. This bidirectional communication is modulated by circadian rhythms and genetic factors. Understanding these pathways offers critical insights into the shared pathophysiology and reveals promising therapeutic targets. Interventions such as neuromodulation, customized exercise programs, and novel treatments focusing on bone-derived signals show potential for simultaneously addressing both mood disorders and bone health deterioration. This review emphasizes the need for an integrated system-based approach in clinical care that moves beyond traditional specialty-focused treatment to improve overall health outcomes, particularly for vulnerable elderly individuals.

## Linked entities

- **Proteins:** bglap2 (bone gamma-carboxyglutamate (gla) protein (osteocalcin) 2)
- **Diseases:** depression (MONDO:0002050), osteoporosis (MONDO:0005298)

## Full-text entities

- **Genes:** BMAL1 (basic helix-loop-helix ARNT like 1) [NCBI Gene 406] {aka ARNTL, ARNTL1, BMAL1c, JAP3, MOP3, PASD3}, Igf2 (insulin-like growth factor 2) [NCBI Gene 16002] {aka Igf-2, Igf-II, M6pr, Mpr, Peg2}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, SOST (sclerostin) [NCBI Gene 50964] {aka CDD, DAND6, SOST1, VBCH}, Ctnnb1 (catenin beta 1) [NCBI Gene 12387] {aka Bfc, Catnb, Mesc}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, TNFSF11 (TNF superfamily member 11) [NCBI Gene 8600] {aka CD254, ODF, OPGL, OPTB2, RANKL, TNLG6B}, LCN2 (lipocalin 2) [NCBI Gene 3934] {aka 24p3, MSFI, NGAL, p25}, CLOCK (clock circadian regulator) [NCBI Gene 9575] {aka KAT13D, bHLHe8}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, Tnfsf11 (tumor necrosis factor (ligand) superfamily, member 11) [NCBI Gene 21943] {aka Ly109l, ODF, OPGL, RANKL, Trance}, IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}, SPP1 (secreted phosphoprotein 1) [NCBI Gene 6696] {aka BNSP, BSPI, ETA-1, OPN}, GPR158 (G protein-coupled receptor 158) [NCBI Gene 57512] {aka mGlyR}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, GSK3B (glycogen synthase kinase 3 beta) [NCBI Gene 2932], BDNF (brain derived neurotrophic factor) [NCBI Gene 627] {aka ANON2, BULN2}, Lcn2 (lipocalin 2) [NCBI Gene 16819] {aka 24p3, NRL, Sip24}, CRH (corticotropin releasing hormone) [NCBI Gene 1392] {aka CRF, CRH1}, TAC1 (tachykinin precursor 1) [NCBI Gene 6863] {aka Hs.2563, NK2, NKNA, NPK, TAC2}, BGLAP (bone gamma-carboxyglutamate protein) [NCBI Gene 632] {aka BGP, OC, OCN}, CALCA (calcitonin related polypeptide alpha) [NCBI Gene 796] {aka CALC1, CGRP, CGRP-I, CGRP-alpha, CGRP1, CT}, POMC (proopiomelanocortin) [NCBI Gene 5443] {aka ACTH, CLIP, LPH, MSH, NPP, OBAIRH}, IL6R (interleukin 6 receptor) [NCBI Gene 3570] {aka CD126, HIES5, IL-1Ra, IL-6R, IL-6R-1, IL-6RA}, ADRB2 (adrenoceptor beta 2) [NCBI Gene 154] {aka ADRB2R, ADRBR, ARB2, B2AR, BAR, BETA2AR}, ESR1 (estrogen receptor 1) [NCBI Gene 2099] {aka ER, ESR, ESRA, ESTRR, Era, NR3A1}
- **Diseases:** comorbidity (MESH:D004194), skeletal degenerative diseases (MESH:D019636), injury to (MESH:D014947), inflammation (MESH:D007249), fracture (MESH:D050723), alcohol abuse (MESH:D000437), behavioral abnormalities (MESH:D001523), AD (MESH:D000544), Skeletal Impairment (MESH:C564967), COVID-19 (MESH:D000086382), neuropsychiatric (MESH:C000631768), knee osteoarthritis (MESH:D020370), bone disease (MESH:D001847), joint (MESH:D007592), Osteoporosis (MESH:D010024), anxiety (MESH:D001007), SCZ (MESH:D012559), health (OMIM:603663), osteoporotic (MESH:D058866), neuroinflammation (MESH:D000090862), HPA axis hyperactivity (MESH:D007029), skeletal damage (MESH:C535850), mood disorders (MESH:D019964), bone metabolic abnormalities (MESH:D001851), skeletal deterioration (OMIM:616592), inflammatory bowel disease (MESH:D015212), Depression (MESH:D003866), IVDD (MESH:D055959), post stroke (MESH:D020521), vitamin D deficiency (MESH:D014808), eating disorders (MESH:D001068), MDD (MESH:D003865), neurological and skeletal disorders (MESH:D009461), osteoarthritis (MESH:D010003), hyperactivity (MESH:D006948), AIS (MESH:D000083242), cognitive impairment (MESH:D003072), memory dysfunction (MESH:D008569)
- **Chemicals:** osteokine (-), melatonin (MESH:D008550), thyroid-stimulating hormones (MESH:D013972), denosumab (MESH:D000069448), teriparatide (MESH:D019379), Catecholamines (MESH:D002395), cortisol (MESH:D006854), PTH (MESH:D010281), norepinephrine (MESH:D009638), serotonin (MESH:D012701), bisphosphonates (MESH:D004164), diosgenin (MESH:D004144)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

83 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938012/full.md

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Source: https://tomesphere.com/paper/PMC12938012