Evidence map›Paper›PMID 18566945›Full record

ArticleJournal of rehabilitation research and development2008

Human genome comparison of paretic and nonparetic vastus lateralis muscle in patients with hemiparetic stroke.

Michael J McKenzie, Shuzhen Yu, Richard F Macko, John C McLenithan, Charlene E Hafer-Macko

Registry-linked trialOpen access · greenAbstract readComparative Study
In one paragraph

Article in Journal of rehabilitation research and development, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00387712 (Inflammatory Abnormalities in Muscle After Stroke), which is not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.5field-weighted citation impact, top 16% 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.

NCT00387712 nacompletednot on this map

Inflammatory Abnormalities in Muscle After Stroke: Effects of Exercise

TypeinterventionalSponsorVA Office of Research and DevelopmentRan2006 to 2014Enrolled99ConditionsStroke, InflammationArmsVelocity based treadmill training, Duration based treadmill training
3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Investigating Muscle Function After Stroke Rehabilitation with 31P-MRS: A Preliminary Study.Medical science monitor : international medical journal of experimental and clinical research · 2018
    Article
  3. Article
  4. Article
  5. Monitoring hemodynamic changes in stroke-affected muscles using near-infrared spectroscopy.Journal of rehabilitation and assistive technologies engineering
    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

5 authors at 1 institution in 1 country.

Michael J McKenzieDivision of Gerontology, University of Maryland School of Medicine, Baltimore, MD, USA.
Shuzhen Yu
Richard F Macko
John C McLenithan
Charlene E Hafer-Macko
University of Maryland, Baltimore · US

Funding

UPPER EXTREMITY TRAINING FOR CHRONIC STROKEP60AG012583 · NIA · UNIVERSITY OF MARYLAND BALTIMORE · PI GOLDBERG, ANDREW P · 1994 to 2005
$7.8M
Diet and Exercise: Race, Postmenopause and MetabolismR01AG019310 · NIA · UNIVERSITY OF MARYLAND BALTIMORE · PI RYAN, ALICE S. · 2001 to 2005
$1.5M
NIA NIH HHS P30-AG-12583NIA NIH HHS P60 AG012583NIA NIH HHS R01 AG019310NIA NIH HHS R01-AG-019310
6 · The paper itself

Abstract

Hemiparetic stroke leads to major skeletal muscle abnormalities, as illustrated by paretic leg atrophy, weakness, and spasticity. Furthermore, the hemiparetic limb muscle shifts to a fast-twitch muscle fiber phenotype with anaerobic metabolism. This study investigated whether skeletal muscle genes were altered in chronic hemiparetic stroke. The nonparetic leg muscle served as an internal control. We used Affymetrix microarray analysis to survey gene expression differences between paretic and nonparetic vastus lateralis muscle punch biopsies from 10 subjects with chronic hemiparetic stroke. Stroke latency was greater than 6 months. We found that 116 genes were significantly altered between the paretic and non paretic vastus lateralis muscles. These gene differences were consistent with reported differences after stroke in areas such as injury and inflammation markers, the myosin heavy chain profile, and high prevalence of impaired glucose tolerance and type 2 diabetes. Furthermore, while many other families of genes were altered, the gene families with the most genes altered included inflammation, cell cycle regulation, signal transduction, metabolism, and muscle contractile protein genes. This study is an early step toward identification of specific gene regulatory pathways that might lead to these differences, propagate disability, and increase vascular disease risk.

Indexed as

AgedAged, 80 and overCell CycleChronic DiseaseFemaleGene ExpressionHumansInflammationLower ExtremityMaleMicroarray AnalysisMiddle AgedMuscle ContractionMuscle, SkeletalParesisRNARNA

Identifiers

PMID18566945
PMCPMC3024241
OpenAlexW2166924858

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.