Evidence map›Paper›PMID 39702559›Full record

ArticleCommunications biology2024

IGF-1 c.258 A > G synonymous mutation ameliorates senile osteoporosis.

Zhaoguo Wang, Dayou Dai, Siyao Wang, Libo Zhang, Yi Li, Xunming Zhang, Yunyun Cheng, Linlin Hao

Abstract read
In one paragraph

Article in Communications biology, 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

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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. Review
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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

8 authors.

Zhaoguo Wang *College of Animal Science, Jilin University, Changchun, Jilin, China.
Dayou Dai *State Key Laboratory of Systems Medicine for Cancer, Shanghai Cancer Institute, Ren Ji Hospital, School of medicine, Shanghai Jiao Tong University, Shanghai, China.
Siyao WangCollege of Animal Science, Jilin University, Changchun, Jilin, China.
Libo ZhangCollege of Animal Science, Jilin University, Changchun, Jilin, China.
Yi LiCollege of Animal Science, Jilin University, Changchun, Jilin, China.
Xunming ZhangCollege of Animal Science, Jilin University, Changchun, Jilin, China.
Yunyun ChengCollege of Animal Science, Jilin University, Changchun, Jilin, China. chengyy@jlu.edu.cn.ORCID 0009-0007-3600-7350
Linlin HaoCollege of Animal Science, Jilin University, Changchun, Jilin, China. haolinlin@jlu.edu.cn.

Funding

National Natural Science Foundation of China (National Science Foundation of China) 32072813
6 · The paper itself

Abstract

Senile osteoporosis (SOP) is a multifactorial, age-related progressive phenomenon with a considerable morbidity and mortality. IGF-1 is an important regulator of bone reconstruction and metabolism throughout life. Nevertheless, our previous study unexpectedly found there is no change in the peak bone mass with a altered IGF-1 gene expression leaded by IGF-1 c.258 A > G synonymous mutation. Considering its involvement in the cellular senescence, we suspected c.258 A > G may participate in SOP. Therefore, the effect of IGF-1 c.258 A > G on SOP was firstly detected, the changes of bone formation and bone resorption index in SOP mice with two genotypes indicated it improved SOP. Then, the in vitro study confirmed the mutation ameliorates SOP by promoting the growth and development of senescent osteoblasts. At last, co-culture of osteoblast and osteoclast further verified the mutation prevents SOP by increasing the bone formation capacity of senescent osteoblasts. Collectively, this study illuminated the role of IGF-1 c.258 A > G in ameliorating SOP.

Indexed as

Insulin-Like Growth Factor IOsteoblastsOsteoporosisAnimalsCellular SenescenceFemaleMaleMiceMice, Inbred C57BLMutationOsteoclastsOsteogenesisinsulin-like growth factor-1, mouseInsulin-Like Growth Factor I

Identifiers

PMID39702559
PMCPMC11659520

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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.