Evidence map›Paper›PMID 26304151›Full record

ArticleBrain : a journal of neurology2015

Reduced gamma-aminobutyric acid concentration is associated with physical disability in progressive multiple sclerosis.

Niamh Cawley, Bhavana S Solanky, Nils Muhlert, Carmen Tur, Richard A E Edden, Claudia A M Wheeler-Kingshott, David H Miller, Alan J Thompson, Olga Ciccarelli

Open access · bronzeAbstract read
In one paragraph

Article in Brain : a journal of neurology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
7.3field-weighted citation impact, top 2% 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

67 citing papers in PubMed, 116 citations in OpenAlex.

  1. Article
  2. Immune-mediated excitotoxicity in brain disorders.Nature reviews. Immunology · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Impact of a GABA-ProducingFASEB bioAdvances · 2026
    Article
  9. Central Dysmyelination in SSADH-Deficient Humans and Mice.Annals of clinical and translational neurology · 2025
    Observational
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

7 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 3 countries.

Niamh Cawley1 NMR Research Unit, Queen Square Multiple Sclerosis Centre, UCL Institute of Neurology, London, UK n.cawley@ucl.ac.uk.
Bhavana S Solanky1 NMR Research Unit, Queen Square Multiple Sclerosis Centre, UCL Institute of Neurology, London, UK.
Nils Muhlert1 NMR Research Unit, Queen Square Multiple Sclerosis Centre, UCL Institute of Neurology, London, UK 2 School of Psychology and Cardiff University Brain Research Imaging Centre, Cardiff University, Cardiff, UK 3 School of Psychological Sciences, University of Manchester, Manchester, UK.
Carmen Tur1 NMR Research Unit, Queen Square Multiple Sclerosis Centre, UCL Institute of Neurology, London, UK.
Richard A E Edden4 Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, MD, USA 5 FM Kirby Centre for Functional Brain Imaging, Kennedy Krieger Institute, Baltimore, MD, USA.
Claudia A M Wheeler-Kingshott1 NMR Research Unit, Queen Square Multiple Sclerosis Centre, UCL Institute of Neurology, London, UK 6 Brain Connectivity Centre, C. Mondino National Neurological Institute, Pavia, Italy.
David H Miller1 NMR Research Unit, Queen Square Multiple Sclerosis Centre, UCL Institute of Neurology, London, UK 7 National Institute of Health Research (NIHR) University College London Hospitals (UCLH) Biomedical Research Centre (BRC), London, UK.
Alan J Thompson1 NMR Research Unit, Queen Square Multiple Sclerosis Centre, UCL Institute of Neurology, London, UK 7 National Institute of Health Research (NIHR) University College London Hospitals (UCLH) Biomedical Research Centre (BRC), London, UK.
Olga Ciccarelli1 NMR Research Unit, Queen Square Multiple Sclerosis Centre, UCL Institute of Neurology, London, UK 7 National Institute of Health Research (NIHR) University College London Hospitals (UCLH) Biomedical Research Centre (BRC), London, UK.
National Hospital for Neurology and Neurosurgery · GBMultiple Sclerosis Society · GBJohns Hopkins University · USNational Institute for Health Research · GB

Funding

NIBIB NIH HHS R01EB015909
6 · The paper itself

Abstract

Neurodegeneration is thought to be the major cause of ongoing, irreversible disability in progressive stages of multiple sclerosis. Gamma-aminobutyric acid is the principle inhibitory neurotransmitter in the brain. The aims of this study were to investigate if gamma-aminobutyric acid levels (i) are abnormal in patients with secondary progressive multiple sclerosis compared with healthy controls; and (ii) correlate with physical and cognitive performance in this patient population. Thirty patients with secondary progressive multiple sclerosis and 17 healthy control subjects underwent single-voxel MEGA-PRESS (MEscher-GArwood Point RESolved Spectroscopy) magnetic resonance spectroscopy at 3 T, to quantify gamma-aminobutyric acid levels in the prefrontal cortex, right hippocampus and left sensorimotor cortex. All subjects were assessed clinically and underwent a cognitive assessment. Multiple linear regression models were used to compare differences in gamma-aminobutyric acid concentrations between patients and controls adjusting for age, gender and tissue fractions within each spectroscopic voxel. Regression was used to examine the relationships between the cognitive function and physical disability scores specific for these regions with gamma-aminobuytric acid levels, adjusting for age, gender, and total N-acetyl-aspartate and glutamine-glutamate complex levels. When compared with controls, patients performed significantly worse on all motor and sensory tests, and were cognitively impaired in processing speed and verbal memory. Patients had significantly lower gamma-aminobutyric acid levels in the hippocampus (adjusted difference = -0.403 mM, 95% confidence intervals -0.792, -0.014, P = 0.043) and sensorimotor cortex (adjusted difference = -0.385 mM, 95% confidence intervals -0.667, -0.104, P = 0.009) compared with controls. In patients, reduced motor function in the right upper and lower limb was associated with lower gamma-aminobutyric acid concentration in the sensorimotor cortex. Specifically for each unit decrease in gamma-aminobutyric acid levels (in mM), there was a predicted -10.86 (95% confidence intervals -16.786 to -4.482) decrease in grip strength (kg force) (P < 0.001) and -8.74 (95% confidence intervals -13.943 to -3.015) decrease in muscle strength (P < 0.006). This study suggests that reduced gamma-aminobutyric acid levels reflect pathological abnormalities that may play a role in determining physical disability. These abnormalities may include decreases in the pre- and postsynaptic components of gamma-aminobutyric acid neurotransmission and in the density of inhibitory neurons. Additionally, the reduced gamma-aminobutyric acid concentration may contribute to the neurodegenerative process, resulting in increased firing of axons, with consequent increased energy demands, which may lead to neuroaxonal degeneration and loss of the compensatory mechanisms that maintain motor function. This study supports the idea that modulation of gamma-aminobutyric acid neurotransmission may be an important target for neuroprotection in multiple sclerosis.See De Stefano and Giorgio (doi:10.1093/brain/awv213) for a scientific commentary on this article.

Indexed as

Multiple SclerosisPersons with DisabilitiesAdultAspartic AcidBrainDisability EvaluationFemalegamma-Aminobutyric AcidGlutamic AcidHumansMagnetic Resonance SpectroscopyMaleMiddle AgedNeuropsychological TestsSeverity of Illness IndexAspartic Acidgamma-Aminobutyric AcidGlutamic Aciddisabilitydisease progressiongamma-aminobutyric acid (GABA)MRImultiple sclerosis

Identifiers

PMID26304151
PMCPMC4643627
OpenAlexW2199931105

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.