Evidence map›Paper›PMID 38591545›Full record

ArticleeLife2024

Deciphering the complex relationship between type 2 diabetes and fracture risk with both genetic and observational evidence.

Pianpian Zhao, Zhifeng Sheng, Lin Xu, Peng Li, Wenjin Xiao, Chengda Yuan, Zhanwei Xu, Mengyuan Yang, Yu Qian, Jiadong Zhong and 3 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

8 citing papers in PubMed, 6 citations in OpenAlex.

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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

13 authors at 8 institutions in 3 countries.

Pianpian Zhao *The affiliated Hangzhou first people's hospital, School of Medicine, Westlake University, Hangzhou, China.ORCID https://orcid.org/0009-0009-1676-1748
Zhifeng Sheng *Health Management Center, The Second Xiangya Hospital of Central South University, Changsha, China.
Lin Xu *Department of Orthopedics, Yantai Affiliated Hospital of Binzhou Medical University, Yantai, China.
Peng LiDepartment of Geratology, The Third People's Hospital of Hangzhou, Hangzhou, China.
Wenjin XiaoDepartment of Endocrinology, Second Affiliated Hospital of Soochow University, Suzhou, China.
Chengda YuanDepartment of Dermatology, Hangzhou Hospital of Traditional Chinese Medicine, Hangzhou, China.
Zhanwei XuCentral Health Center of Mashenqiao Town, Tianjin, China.
Mengyuan YangThe affiliated Hangzhou first people's hospital, School of Medicine, Westlake University, Hangzhou, China.
Yu QianThe affiliated Hangzhou first people's hospital, School of Medicine, Westlake University, Hangzhou, China.
Jiadong ZhongThe affiliated Hangzhou first people's hospital, School of Medicine, Westlake University, Hangzhou, China.
Jiaxuan GuThe affiliated Hangzhou first people's hospital, School of Medicine, Westlake University, Hangzhou, China.
David KarasikAzrieli Faculty of Medicine, Bar-Ilan University, Safed, Israel.
Hou-Feng ZhengThe affiliated Hangzhou first people's hospital, School of Medicine, Westlake University, Hangzhou, China.ORCID https://orcid.org/0000-0001-5681-8598
Westlake University · CNBar-Ilan University · ILBinzhou Medical University · CNCentral South University · CNHangzhou Hospital of Traditional Chinese Medicine · CNHealth Center · USSoochow University · CNThird People's Hospital of Hangzhou · CN

Funding

National Natural Science Foundation of China 82370887The Chinese National Key Technology R&D Program, Ministry of Science and Technology 2021YFC2501702The "Pioneer" and "Leading Goose" R&D Program of Zhejiang 2023C03164The "Pioneer" and "Leading Goose" R&D Program of Zhejiang 2024SSYS0032The Westlake Laboratory of Life Sciences and Biomedicine 202208014
6 · The paper itself

Abstract

The 'diabetic bone paradox' suggested that type 2 diabetes (T2D) patients would have higher areal bone mineral density (BMD) but higher fracture risk than individuals without T2D. In this study, we found that the genetically predicted T2D was associated with higher BMD and lower risk of fracture in both weighted genetic risk score (wGRS) and two-sample Mendelian randomization (MR) analyses. We also identified ten genomic loci shared between T2D and fracture, with the top signal at SNP rs4580892 in the intron of gene

Indexed as

Diabetes Mellitus, Type 2Fractures, BoneBone and BonesGenome-Wide Association StudyHumansProspective StudiesRisk FactorsfracturegeneticsgenomicshumanMendelian randomization analysesobservational analysestype 2 diabetes

Identifiers

PMID38591545
PMCPMC11003741
OpenAlexW4386163057

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.