Evidence map›Paper›PMID 36362274›Full record

SynthesisInternational journal of molecular sciences2022

Molecular and Genetic Mechanisms of Spinal Stenosis Formation: Systematic Review.

Vadim A Byvaltsev, Andrei A Kalinin, Phillip A Hernandez, Valerii V Shepelev, Yurii Y Pestryakov, Marat A Aliyev, Morgan B Giers

Open access · goldAbstract readSystematic Review
In one paragraph

Synthesis in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
5.4field-weighted citation impact, top 3% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Pooled it
  2. Integrative Transcriptomic Profiling Delineates LTBP4-Driven Fibroblast Reprogramming Across the Ossification Continuum of the Ligamentum Flavum.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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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

7 authors at 3 institutions in 3 countries.

Vadim A ByvaltsevDepartment of Neurosurgery, Irkutsk State Medical University, Irkutsk 664003, Russia.ORCID 0000-0003-4349-7101
Andrei A KalininDepartment of Neurosurgery, Irkutsk State Medical University, Irkutsk 664003, Russia.
Phillip A HernandezSchool of Chemical, Biological, and Environmental Engineering, Oregon State University, Corvallis, OR 97331, USA.
Valerii V ShepelevDepartment of Neurosurgery, Irkutsk State Medical University, Irkutsk 664003, Russia.
Yurii Y PestryakovDepartment of Neurosurgery, Irkutsk State Medical University, Irkutsk 664003, Russia.
Marat A AliyevDepartment of Neurosurgery, Asfendiyarov Kazakh National Medical University, Almaty 050012, Kazakhstan.
Morgan B GiersSchool of Chemical, Biological, and Environmental Engineering, Oregon State University, Corvallis, OR 97331, USA.ORCID 0000-0002-2247-1167
Irkutsk State Medical University · RUOregon State University · USKazakh National Medical University · KZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spinal stenosis (SS) is a multifactorial polyetiological condition characterized by the narrowing of the spinal canal. This condition is a common source of pain among people over 50 years old. We perform a systematic review of molecular and genetic mechanisms that cause SS. The five main mechanisms of SS were found to be ossification of the posterior longitudinal ligament (OPLL), hypertrophy and ossification of the ligamentum flavum (HLF/OLF), facet joint (FJ) osteoarthritis, herniation of the intervertebral disc (IVD), and achondroplasia. FJ osteoarthritis, OPLL, and HLF/OLFLF/OLF have all been associated with an over-abundance of transforming growth factor beta and genes related to this phenomenon. OPLL has also been associated with increased bone morphogenetic protein 2. FJ osteoarthritis is additionally associated with Wnt/β-catenin signaling and genes. IVD herniation is associated with collagen type I alpha 1 and 2 gene mutations and subsequent protein dysregulation. Finally, achondroplasia is associated with fibroblast growth factor receptor 3 gene mutations and fibroblast growth factor signaling. Although most publications lack data on a direct relationship between the mutation and SS formation, it is clear that genetics has a direct impact on the formation of any pathology, including SS. Further studies are necessary to understand the genetic and molecular changes associated with SS.

Indexed as

AchondroplasiaLigamentum FlavumOssification of Posterior Longitudinal LigamentOsteoarthritisSpinal StenosisHumansMiddle Agedcongenital diseasedegenerative diseasegeneticsmolecular mechanismsspinal stenosissystematic review

Identifiers

PMID36362274
PMCPMC9658491
OpenAlexW4308335814

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.