Evidence map›Paper›PMID 18372305›Full record

ArticleThe Journal of physiology2008

Physiological properties of human diaphragm muscle fibres and the effect of chronic obstructive pulmonary disease.

Alison K Stubbings, Alastair J Moore, Michael Dusmet, Peter Goldstraw, Timothy G West, Michael I Polkey, Michael A Ferenczi

Open access · greenAbstract readComparative Study
In one paragraph

Article in The Journal of physiology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.9field-weighted citation impact, top 5% 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

19 citing papers in PubMed, 71 citations in OpenAlex.

  1. Unaffected contractility of diaphragm muscle fibers in humans on mechanical ventilation.American journal of physiology. Lung cellular and molecular physiology · 2014
    Trial
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Impact of diaphragm muscle fiber atrophy on neuromotor control.Respiratory physiology & neurobiology · 2013
    Review
  14. Article
  15. Muscle function in COPD: a complex interplay.International journal of chronic obstructive pulmonary disease · 2012
    Review
  16. Article
  17. In vivo specific tension of the human quadriceps femoris muscle.European journal of applied physiology · 2009
    Article
  18. Respiratory muscle fiber remodeling in chronic hyperinflation: dysfunction or adaptation?Journal of applied physiology (Bethesda, Md. : 1985) · 2009
    Review
  19. Skeletal muscle dysfunction in patients with chronic obstructive pulmonary disease.International journal of chronic obstructive pulmonary disease · 2008
    Review
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 2 institutions in 1 country.

Alison K StubbingsMolecular Medicine Section, National Heart & Lung Institute, Imperial College London, South Kensington Campus, London SW7 2AZ, UK.
Alastair J Moore
Michael Dusmet
Peter Goldstraw
Timothy G West
Michael I Polkey
Michael A Ferenczi
Royal Brompton Hospital · GBImperial College London · GB

Funding

Medical Research Council G0100150
6 · The paper itself

Abstract

The contractile and actomyosin ATPase properties of single fibres were examined in human diaphragm muscle obtained from patients with and without chronic obstructive pulmonary disease (COPD). Costal diaphragm biopsies were taken from five patients without evidence of COPD and from 11 age-matched individuals with varying degrees of the disease. Our aim was to establish whether changes in contractile properties of COPD diaphragm could be fully explained by the previously documented shift towards a greater proportion of type I myosin heavy chain isoform in COPD. The relative proportion of type I diaphragm fibres from non-COPD and COPD patients was measured by gel electrophoresis, and was negatively correlated with FEV(1) over the full range of values investigated. There was also significant atrophy of the type I fibre population in COPD diaphragms. Isometric tension was similar among the fibre types and between the COPD and non-COPD patients. The intrinsic energetic properties of diaphragm fibres were examined by monitoring the time-resolved actomyosin ATPase activity in COPD and non-COPD fibres that produced similar isometric forces. The isometric ATPase rate in COPD fibres was reduced to 50% of the rate in non-COPD fibres; hence, the cost of isometric contraction in type I and type IIA COPD fibres was reduced to between one-third and one-half of the tension cost calculated for non-COPD fibres. The rate of force development in type I COPD fibres was reduced to 50% of the rate seen in non-COPD type-I fibres. No difference in the rate of ATP consumption between COPD and non-COPD fibres was evident during isovelocity shortening. These data extend previous findings showing that aspects of breathing mechanics during progressive COPD are associated with remodelling of the diaphragm fibre-type distribution; on top of the increase in type I fibres there are fibre-specific reductions in force development rate (type I fibres) and ATPase rate that are consistent with the impairment of cross-bridge cycling kinetics.

Indexed as

AdultAgedAged, 80 and overDiaphragmFemaleForced Expiratory VolumeHumansIsometric ContractionMaleMiddle AgedMuscle Fibers, SkeletalPulmonary Disease, Chronic Obstructive

Identifiers

PMID18372305
PMCPMC2464347
OpenAlexW1555649237

What OpenQuestion holds

Textmetadata
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.