Evidence map›Paper›PMID 41697318›Full record

ReviewJournal of bone and mineral metabolism2026

Endothelial diversity in bone vasculature coordinates osteogenesis and hematopoiesis.

Takahito Iga

Abstract readReview
PubMed Publisher
In one paragraph

Review in Journal of bone and mineral metabolism, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author.

Takahito IgaDepartment of Orthopedic Surgery, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582, Japan. takahito0429@keio.jp.ORCID http://orcid.org/0000-0002-7869-7421

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone is a highly vascularized organ, and the vasculature in bone not only delivers oxygen and nutrients but also helps determine when and where bone forms, how the marrow is organized, and how hematopoietic stem cells (HSCs) are maintained. Over the past decade, research has shifted from a single, uniform view of bone vessels to site- and stage-specific endothelial programs along the metaphysis-diaphysis-epiphysis axis of long bones. Local endothelial identity and hemodynamic signals coordinate angiogenesis with osteogenesis and shape the marrow niche. These programs also shift with aging. This review summarizes the recent advances in these endothelial programs and their roles in bone growth and hematopoiesis. Considering the vasculature as an active driver of skeletal integrity and hematopoietic function suggests strategies to strengthen bone, reduce skeletal fragility, and sustain hematopoiesis. This framework provides a roadmap for future studies and clinical translation.

Indexed as

Bone and BonesEndothelial CellsHematopoiesisNeovascularization, PhysiologicOsteogenesisAngiogenesisAnimalsHematopoietic Stem CellsHumansAngiogenesisBone vasculatureEndothelial heterogeneityHematopoietic stem cellOsteogenesis

Identifiers

What OpenQuestion holds

Textmetadata
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.