Evidence map›Paper›PMID 36819520›Full record

ArticleAnnals of translational medicine2023

Qian Song, Dongming Zhou, Jianyang Du, Tao Li, Xueyu He, Jianxiong Wang, Aijun Chao, Bingbing Yu, Chunyan Shan

Open access · diamondAbstract read
In one paragraph

Article in Annals of translational medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.8field-weighted citation impact, top 11% of its field
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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. 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

9 authors at 6 institutions in 1 country.

Qian Song *Department of Osteo-internal Medicine, Tianjin Hospital, Tianjin, China.
Dongming Zhou *Department of Traumatic Orthopedics, The First Affiliated Hospital of Baotou Medical College, Inner Mongolia University of Science and Technology, Baotou, Inner Mongolia Autonomous Region, China.
Jianyang Du *Department of Neurosurgery, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China.
Tao LiDepartment of Orthopedics, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Shenshan Central Hospital, Shanwei, China.
Xueyu HeDepartment of Pediatrics, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Shenshan Central Hospital, Shanwei, China.
Jianxiong WangDepartment of Endocrinology, Tianjin Hospital, Tianjin, China.
Aijun ChaoDepartment of Osteo-internal Medicine, Tianjin Hospital, Tianjin, China.
Bingbing YuDepartment of Orthopedics, The Fifth Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Chunyan ShanDepartment of Nephrology, Tianjin Medical University, Chu Hsien-I Memorial Hospital & Tianjin Institute of Endocrinology, NHC Key Laboratory of Hormones and Development, Tianjin Key Laboratory of Metabolic Diseases, Tianjin, China.
Tianjin Hospital · CNSun Yat-sen University · CNGuangzhou Medical University · CNInner Mongolia University of Science and Technology · CNShandong Provincial Hospital · CNTianjin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Although Methods: Ovariectomy (OVX)-induced estrogen deficiency-related osteoporotic mouse models and sham mouse models were established using 8-week-old female C57BL/6J mice. Micro-computed tomography (µCT) scanning was performed to assess the skeletal phenotype. The differentiation potential of bone marrow mesenchymal stem cells (BMSCs) from the OVX and sham groups was assessed by osteogenic or adipogenic induction medium Results: µCT scanning showed that AP treatment attenuated the osteoporotic phenotype in OVX-induced estrogen deficiency-related osteoporotic mice. The results of ARS staining, ALP staining, ORO staining and quantitative real-time polymerase chain reaction indicated that BMSCs from OVX-induced osteoporotic mice displayed a significant reduction in osteogenic differentiation and an increase in adipogenic differentiation, which could be reversed by AP treatment. Conclusions: Our findings suggested that AP regulated the differentiation potential of BMSCs and ameliorated the development of estrogen deficiency-related osteoporosis, which might be an effective therapeutic method for estrogen deficiency-related osteoporosis.

Indexed as

Andrographis paniculata (AP)bone lossbone marrow mesenchymal stem cells (BMSCs)osteoporosis

Identifiers

PMID36819520
PMCPMC9929840
OpenAlexW4320012086

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.