Evidence map›Paper›PMID 19228968›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2009

Carriers of recessive WNK1/HSN2 mutations for hereditary sensory and autonomic neuropathy type 2 (HSAN2) are more sensitive to thermal stimuli.

Marco L Loggia, M Catherine Bushnell, Martine Tétreault, Isabelle Thiffault, Claude Bhérer, Nazma K Mohammed, Anil A Kuchinad, Audrey Laferrière, Marie-Josée Dicaire, Lina Loisel and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 35% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Trial
  2. Genetic pain loss disorders.Nature reviews. Disease primers · 2022
    Review
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  4. Article
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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

12 authors at 3 institutions in 2 countries.

Marco L LoggiaAlan Edwards Centre for Research on Pain, McGill University, Montreal, Quebec, Canada H3A 2B2. marco@nmr.mgh.harvard.edu
M Catherine Bushnell
Martine Tétreault
Isabelle Thiffault
Claude Bhérer
Nazma K Mohammed
Anil A Kuchinad
Audrey Laferrière
Marie-Josée Dicaire
Lina Loisel
Jeffrey S Mogil
Bernard Brais
Centre Hospitalier de l’Université de Montréal · CAEdwards (United Kingdom) · GBMcGill University · CA

Funding

Risk Factors for Onset and Persistence of TMDU01DE017018 · NIDCR · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DIATCHENKO, LUDA, FILLINGIM, ROGER B · 2005 to 2016
$35.9M
Sex-Related Genetic Influences on Pain and AnalgesiaR01NS041670 · NINDS · UNIVERSITY OF FLORIDA · PI FILLINGIM, ROGER B · 2000 to 2009
$4.4M
NIDCR NIH HHS U01 DE017018NINDS NIH HHS R01 NS041670
6 · The paper itself

Abstract

Hereditary sensory and autonomic neuropathy type 2 (HSAN2) is a rare recessive genetic disorder characterized by severe sensory loss affecting the tactile, thermal and nociceptive modalities. Although heterozygous carriers of nonsense mutations in the HSN2 gene, called with-no-lysine(K)-1 (WNK1), do not develop the disease, historical and experimental evidence suggests that these individuals might perceive somatosensory stimuli differently from others. Using the method-of-limits, we assessed the thresholds for warmth detection, cool detection, heat pain and cold pain in 25 mutation carriers and 35 controls. In group analyses, carriers displayed significantly lower warmth (p<0.001) and cool (p<0.05) difference thresholds, and also tended to report cold pain at higher temperatures (p=0.095), than controls. Similarly, matched-pair analyses showed that carriers are significantly more sensitive to warm stimuli (p<0.01) and cold pain stimuli (p<0.05), and tend to be more sensitive to cool stimuli (p=0.11). Furthermore, the differences between the warmth detection thresholds of the carriers and those of gender- and sex-matched wild types significantly increased with age (r=0.76, p=0.02), and in carriers cool detection thresholds did not increase with age (r=0.27, p=0.24) as expected and observed in controls (r=0.34, p=0.05). This study demonstrates that the carriers of a recessive mutation for HSAN2 display greater sensitivity to innocuous thermal stimuli, as well as for cold pain, suggesting a possible environmental adaptive advantage of the heterozygous state.

Indexed as

AdultAgedDNA Mutational AnalysisFemaleGene FrequencyGenes, RecessiveGenetic Predisposition to DiseaseGenetic TestingGenotypeHereditary Sensory and Autonomic NeuropathiesHumansHyperalgesiaIntracellular Signaling Peptides and ProteinsMaleMiddle AgedMinor Histocompatibility AntigensIntracellular Signaling Peptides and ProteinsMinor Histocompatibility AntigensNerve Tissue ProteinsProtein Serine-Threonine KinasesWNK1 protein, humanWNK Lysine-Deficient Protein Kinase 1

Identifiers

PMID19228968
PMCPMC2749662
OpenAlexW2041191850

What OpenQuestion holds

Textmetadata
LicenceTDM
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.