Evidence map›Paper›PMID 36339402›Full record

ReviewFrontiers in endocrinology2022

Necroptosis: A new target for prevention of osteoporosis.

Xinli Hu, Zheng Wang, Chao Kong, Yu Wang, Weiguo Zhu, Wei Wang, Yongjin Li, Wei Wang, Shibao Lu

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in endocrinology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

13 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
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  8. Journal of musculoskeletal & neuronal interactions · 2025
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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

9 authors at 1 institution in 1 country.

Xinli HuDepartment of Orthopedics, Xuanwu Hospital, Capital Medical University, Beijing, China.
Zheng WangDepartment of Orthopedics, Xuanwu Hospital, Capital Medical University, Beijing, China.
Chao KongDepartment of Orthopedics, Xuanwu Hospital, Capital Medical University, Beijing, China.
Yu WangDepartment of Orthopedics, Xuanwu Hospital, Capital Medical University, Beijing, China.
Weiguo ZhuDepartment of Orthopedics, Xuanwu Hospital, Capital Medical University, Beijing, China.
Wei WangDepartment of Orthopedics, Xuanwu Hospital, Capital Medical University, Beijing, China.
Yongjin LiDepartment of Orthopedics, Xuanwu Hospital, Capital Medical University, Beijing, China.
Wei WangDepartment of Orthopedics, Xuanwu Hospital, Capital Medical University, Beijing, China.
Shibao LuDepartment of Orthopedics, Xuanwu Hospital, Capital Medical University, Beijing, China.
Capital Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple causes may contribute to osteoporosis, characterized by a loss in bone mass and density as a consequence of the degradation of bone microstructure and a resultant rise in bone fragility. Recently, increasing attention has been paid to the role of necroptosis in the development of osteoporosis. Necroptosis is orchestrated by a set of proteins known as receptor-interacting protein kinase (RIPK)1, RIPK3, and mixed lineage kinase domain-like protein (MLKL). A necrosome is formed by MLKL, RIPK1, RIPK3, and RIPK3-RIPK3. A dissociated MLKL forms pores in the plasma membrane and eventually leads to necroptosis after translocating from the necrosome. In this review, we discuss a detailed understanding of necroptosis and its associated processes, a better understanding of its interactions with osteoclasts, osteoblasts, and osteocytes, and the associations between necroptosis and diabetic osteoporosis, steroid-induced osteoporosis, and postmenopausal osteoporosis. In addition, a variety of experimental medicines capable of modulating crucial necroptosis processes are highlighted. It's important to note that this is the first review paper to consolidate current data on the role of necroptosis in osteoporosis, and it offers fresh hope for the future treatment of this disease.

Indexed as

NecroptosisOsteoporosisHumansProtein KinasesProtein Kinasescell deathnecroptosisosteoblastsosteoclastsosteoporosis

Identifiers

PMID36339402
PMCPMC9627214
OpenAlexW4306842416

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.