Evidence map›Paper›PMID 39445778›Full record

ArticleEndocrinology2024

Evaluation of Osteogenic Phenotype in Postmenopausal Women Receiving Anabolic and Antiresorptive Osteoporosis Therapies.

Margaret M Kobelski, Sabashini K Ramchand, Joy N Tsai, Benjamin Z Leder, Marie B Demay

Abstract read
In one paragraph

Article in Endocrinology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Comparative bone histomorphometry effects of combined denosumab and teriparatide vs monotherapy in postmenopausal women with osteoporosis: a randomized controlled trial.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2026
    Trial
  2. Article
  3. Article
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

5 authors.

Margaret M KobelskiEndocrine Unit, Massachusetts General Hospital, Boston, MA 02114, USA.
Sabashini K RamchandEndocrine Unit, Massachusetts General Hospital, Boston, MA 02114, USA.
Joy N TsaiEndocrine Unit, Massachusetts General Hospital, Boston, MA 02114, USA.
Benjamin Z LederEndocrine Unit, Massachusetts General Hospital, Boston, MA 02114, USA.
Marie B DemayEndocrine Unit, Massachusetts General Hospital, Boston, MA 02114, USA.ORCID 0000-0001-5845-5479

Funding

The Harvard Clinical and Translational Science CenterUL1TR002541 · NCATS · HARVARD MEDICAL SCHOOL · PI NADLER, LEE MARSHALL · 2018 to 2022
$93.0M
Translational Imaging and Phenotyping CoreP30AR075042 · NIAMS · MASSACHUSETTS GENERAL HOSPITAL · PI MARY L BOUXSEIN, PAOLA DIVIETI PAJEVIC · 2019 to 2026
$7.4M
Mechanisms Underlying the Bone Modeling Effects of Combined Anabolic/Antiresorptive AdministrationR01AR073191 · NIAMS · MASSACHUSETTS GENERAL HOSPITAL · PI DEMAY, MARIE, LEDER, BENJAMIN Z · 2019 to 2022
$2.2M
NCATS NIH HHS UL1 TR002541NIAMS NIH HHS P30 AR075042NIAMS NIH HHS R01 AR073191NIH HHS R01 AR073191NIH's National Center for Advancing Translational Sciences 1UL1TR002541-01
6 · The paper itself

Abstract

Aging of the general population has led to a substantial increase in the prevalence of osteoporosis over the past decades. While there are effective pharmacological agents that increase bone formation, decrease bone resorption, and decrease fracture risk, they do not uniformly cure osteoporosis. This has prompted investigations to examine whether combination therapy (COMBO) with these agents can result in an additive benefit. Since concomitant therapy with denosumab and teriparatide has shown promise in this respect, investigations were undertaken to explore whether the changes in osteogenic phenotype could provide insight into the cellular and molecular mechanism of this effect. Investigations were performed in postmenopausal women receiving denosumab, teriparatide, or both for 3 months. Histomorphometric parameters were the primary outcome, while exploratory studies examined RNA expression in bone biopsies as well as in sorted and cultured bone marrow stromal cells (BMSCs). Osteogenic colony forming units of BMSCs were also evaluated. The studies demonstrated that COMBO results in an increase in osteoprogenitors, evidenced by an increase in osteoblastic colony-forming units. This was associated with an increased in BMSC expression of LGR6 (leucine-rich repeat containing G protein-coupled receptor 6), a stem cell marker and activator of the canonical Wnt signaling pathway. These data suggest that enhancement of canonical Wnt signaling contributes to the increase in osteoprogenitors and consequently an increase in bone density in postmenopausal women receiving COMBO for osteoporosis.

Indexed as

Bone Density Conservation AgentsDenosumabOsteogenesisOsteoporosis, PostmenopausalTeriparatideAgedAnabolic AgentsDrug Therapy, CombinationFemaleHumansMesenchymal Stem CellsMiddle AgedPhenotypePostmenopauseReceptors, G-Protein-CoupledAnabolic AgentsBone Density Conservation AgentsDenosumabReceptors, G-Protein-CoupledTeriparatideanabolicantiresorptivebone marrow stromal cellsLGR6osteoporosis

Identifiers

PMID39445778
PMCPMC11523613

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.