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Closing the care gap: IOF position paper identifies barriers and solutions to global undertreatment of osteoporosis

The International Osteoporosis Foundation identifies critical global barriers to osteoporosis care, including limited DXA scanning and outdated treatment criteria. The IOF advocates for a paradigm shift in bone health management worldwide, recognizing high fracture risk as a valid criterion for treatment and reimbursement.

SourceInternational Osteoporosis Foundation·JournalOsteoporosis International·TypeLiterature review·DateSep 9, 2025

Therapeutic potential for PEPITEM in osteoporosis

Researchers from the University of Birmingham identified bioactive peptide sequences in PEPITEM that counteract key changes caused by osteoporosis. The study shows the full PEPITEM molecule reduces bone resorption, increases bone formation, and promotes angiogenesis in bone.

SourceUniversity of Birmingham·JournalBiomedicine & Pharmacotherapy·TypeExperimental study·DateSep 2, 2025

Nucleic acid aptamers for advancing targeted therapies for bone diseases

Researchers explore the benefits of nucleic acid aptamers in targeted therapies for bone tissue regeneration, revealing their potential in managing orthopedic conditions. Aptamers can modulate key molecular pathways involved in bone repair, advancing the standard of care for fractures and various types of bone diseases.

SourceEditorial Office of West China School of Stomatology, Sichuan University·JournalBone Research·TypeLiterature review·DateAug 26, 2025

Genetically engineered mouse model provides insights on genetic bone disorders

Researchers developed a genetically modified mouse model to study osteogenesis imperfecta (OI), a rare genetic bone disorder. The study found that the Sp7 R342C mutation affects bone mineral density, trabecular bone volume fraction, and cortical porosity, leading to impaired bone remodeling.

SourceEditorial Office of West China School of Stomatology, Sichuan University·JournalBone Research·TypeExperimental study·DateAug 12, 2025

Researchers identify protein essential for balancing bone tissue

A team of researchers from the University of São Paulo identified agrin as a crucial protein in maintaining bone mass and quality. The study found that osteocytes produce agrin, which plays an essential role in preserving bone health. Without agrin, bone tissue becomes less dense and more fragile, making bones susceptible to fractures.

SourceFundação de Amparo à Pesquisa do Estado de São Paulo·JournalInternational Journal of Biological Macromolecules·DateJun 25, 2025

New review highlights impact of diabetes on bone health and fracture risk

A landmark review highlights how diabetes alters bone microarchitecture and increases fracture risk in people with type 2 diabetes, despite normal or elevated bone mineral density. The authors advocate for updated diagnostic tools, including a revised TBS algorithm, to more accurately reflect bone quality in individuals with central ob...

SourceInternational Osteoporosis Foundation·JournalOsteoporosis International·TypeLiterature review·DateJun 18, 2025

Aging disrupts osteocyte networks and bone structure, with greater impact in males

Researchers used a premature aging mouse model to study the effects of age and sex on osteocyte networks and bone structure. Aged PolgA mice showed accelerated skeletal aging, reduced osteocyte connectivity, and increased frailty, with males exhibiting more pronounced changes.

SourceEditorial Office of West China School of Stomatology, Sichuan University·JournalBone Research·TypeExperimental study·DateJun 10, 2025

Joint consensus highlights the role of bone turnover markers in osteoporosis diagnosis and management

A new consensus paper emphasizes the role of bone turnover markers (BTMs) in diagnosing and managing osteoporosis. BTMs, such as procollagen type I N propeptide (PINP) and β-isomerized C-terminal telopeptide of type I collagen (β-CTX-I), are invaluable tools for predicting fracture risk and monitoring treatment adherence.

SourceInternational Osteoporosis Foundation·JournalOsteoporosis International·TypeLiterature review·DateMar 31, 2025

Hard evidence of soft teeth: the oral symptoms of hypophosphatasia

Researchers from Osaka University analyzed dental issues faced by Japanese patients with hypophosphatasia, finding two distinct groups: odonto-type disease (early tooth loss) and non-odonto-type disease (tooth misalignment and softening). The study aims to improve diagnosis and treatment for this often misunderstood disease.

SourceOsaka University·JournalScientific Reports·TypeObservational study·DateMar 10, 2025

Nemours Children’s study demonstrates babies prenatally diagnosed with lethal osteogenesis imperfecta may survive with medical interventions

A new study by Nemours Children's Health reveals that prenatal diagnosis of OI does not accurately predict mortality, and many babies can survive with medical interventions. The study found that 16 out of 18 infants with lethal OI diagnoses survived and achieved significant mobility milestones.

SourceNemours·JournalJBMR Plus·TypeObservational study·DateMar 4, 2025

Gene therapy may be “one shot stop” for rare bone disease

A new study adds weight to the safety and effectiveness of a gene therapy for hypophosphatasia, a rare inherited disorder that causes abnormal bone development. The treatment, AAV8-TNAP-D10, has shown promising results in mice models, with female mice achieving improvements in bone and teeth at lower doses.

SourceSanford Burnham Prebys·JournalJournal of Bone and Mineral Research·TypeExperimental study·DateFeb 3, 2025

The European Society For Paediatric Endocrinology and the European Society Of Endocrinology join together in 2025 to launch the first joint Congress – “Connecting Endocrinology Across The Life Course”

The European Society for Paediatric Endocrinology and the European Society of Endocrinology will host the first-ever joint Congress on May 10-13, 2025. The event aims to bring together paediatric and adult endocrine specialists from across Europe and the world to collaborate and celebrate endocrinology.

Special issue: Osteogenesis imperfecta from bench to bedside and from cradle to grave

This special issue of Calcified Tissue International presents a collection of critical reviews and original research articles on osteogenesis imperfecta (OI), covering essential aspects of the condition, including its nosology, genetics, and clinical presentation. The contributions also discuss treatment strategies for both children an...

SourceInternational Osteoporosis Foundation·TypeCommentary/editorial·DateNov 29, 2024

Opioids may negatively impact hormone health

The Endocrine Society's new statement highlights research gaps on opioids' effects on the endocrine system, which can lead to conditions like male hypogonadism and secondary adrenal insufficiency. Clinicians need to monitor patients using opioids for signs of these health consequences.

SourceThe Endocrine Society·JournalEndocrine Reviews·DateOct 24, 2024

Zebrafish as a model for studying rare genetic disease

A recent study employs zebrafish to model Nager syndrome, revealing the role of sf3b4 mutations in facial development and apoptosis. The research suggests that FGF8 plays a critical role in disease pathogenesis and provides a potential therapeutic strategy.

SourceKyushu University·JournalInternational Journal of Biological Macromolecules·TypeExperimental study·DateOct 16, 2024

Research findings offer a unique opportunity for early diagnosis and therapeutic intervention for rheumatoid arthritis

Researchers propose a better understanding of inflammation in rheumatoid arthritis, identifying an early pathogenic macrophage cell/gene signature that shapes the inflammatory environment. This discovery offers a unique opportunity for early diagnosis and therapeutic intervention, potentially leading to improved patient outcomes.

SourceTrinity College Dublin·JournalScience Advances·TypeMeta-analysis·DateSep 27, 2024