Evidence map›Paper›PMID 32651949›Full record

ArticleBrain : a journal of neurology2020

Molecular and cellular correlates of human nerve regeneration: ADCYAP1/PACAP enhance nerve outgrowth.

Georgios Baskozos, Oliver Sandy-Hindmarch, Alex J Clark, Katherine Windsor, Pall Karlsson, Greg A Weir, Lucy A McDermott, Joanna Burchall, Akira Wiberg, Dominic Furniss and 2 more

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Brain : a journal of neurology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 41 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 3 pooled it
4.5field-weighted citation impact, top 4% 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

41 citing papers in PubMed, 3 syntheses or guidelines pooled it, 81 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 2 countries.

Georgios BaskozosNuffield Department of Clinical Neurosciences, The University of Oxford, Oxford, UK.
Oliver Sandy-HindmarchNuffield Department of Clinical Neurosciences, The University of Oxford, Oxford, UK.
Alex J ClarkNuffield Department of Clinical Neurosciences, The University of Oxford, Oxford, UK.
Katherine WindsorNuffield Department of Clinical Neurosciences, The University of Oxford, Oxford, UK.
Pall KarlssonDepartment of Clinical Medicine, The Danish Pain Research Center, Aarhus, Denmark.
Greg A WeirNuffield Department of Clinical Neurosciences, The University of Oxford, Oxford, UK.
Lucy A McDermottNuffield Department of Clinical Neurosciences, The University of Oxford, Oxford, UK.
Joanna BurchallNuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, The University of Oxford, Oxford, UK.
Akira WibergNuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, The University of Oxford, Oxford, UK.
Dominic FurnissNuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, The University of Oxford, Oxford, UK.
David L H BennettNuffield Department of Clinical Neurosciences, The University of Oxford, Oxford, UK.
Annina B SchmidNuffield Department of Clinical Neurosciences, The University of Oxford, Oxford, UK.
University of Oxford · GBNuffield Orthopaedic Centre · GBDanish Pain Research Center · DK

Funding

Medical Research Council MR/N001524/1Medical Research Council MR/T01072X/1Wellcome 095698Z/11/ZWellcome 202747/Z/16/ZWellcome TrustWellcome Trust 097152/Z/11/ZWellcome Trust 203141/Z/16/Z
6 · The paper itself

Abstract

We only have a rudimentary understanding of the molecular and cellular determinants of nerve regeneration and neuropathic pain in humans. This cohort study uses the most common entrapment neuropathy (carpal tunnel syndrome) as a human model system to prospectively evaluate the cellular and molecular correlates of neural regeneration and its relationship with clinical recovery. In 60 patients undergoing carpal tunnel surgery [36 female, mean age 62.5 (standard deviation 12.2) years], we used quantitative sensory testing and nerve conduction studies to evaluate the function of large and small fibres before and 6 months after surgery. Clinical recovery was assessed with the global rating of change scale and Boston Carpal Tunnel Questionnaire. Twenty healthy participants provided normative data [14 female, mean age 58.0 (standard deviation 12.9) years]. At 6 months post-surgery, we noted significant recovery of median nerve neurophysiological parameters (P < 0.0001) and improvements in quantitative sensory testing measures of both small and large nerve fibre function (P < 0.002). Serial biopsies revealed a partial recovery of intraepidermal nerve fibre density [fibres/mm epidermis pre: 4.20 (2.83), post: 5.35 (3.34), P = 0.001], whose extent correlated with symptom improvement (r = 0.389, P = 0.001). In myelinated afferents, nodal length increased postoperatively [pre: 2.03 (0.82), post: 3.03 (1.23), P < 0.0001] suggesting that this is an adaptive phenomenon. Transcriptional profiling of the skin revealed 31 differentially expressed genes following decompression, with ADCYAP1 (encoding pituitary adenylate cyclase activating peptide, PACAP) being the most strongly upregulated (log2 fold-change 1.87, P = 0.0001) and its expression was associated with recovery of intraepidermal nerve fibres. We found that human induced pluripotent stem cell-derived sensory neurons expressed the receptor for PACAP and that this peptide could significantly enhance axon outgrowth in a dose-dependent manner in vitro [neurite length PACAP 1065.0 µm (285.5), vehicle 570.9 μm (181.8), P = 0.003]. In conclusion, carpal tunnel release is associated with significant cutaneous reinnervation, which correlates with the degree of functional improvement and is associated with a transcriptional programme relating to morphogenesis and inflammatory processes. The most highly dysregulated gene ADCYAP1 (encoding PACAP) was associated with reinnervation and, given that this peptide signals through G-protein coupled receptors, this signalling pathway provides an interesting therapeutic target for human sensory nerve regeneration.

Indexed as

AdultAgedCarpal Tunnel SyndromeCohort StudiesFemaleHumansInduced Pluripotent Stem CellsMaleMiddle AgedNerve RegenerationPituitary Adenylate Cyclase-Activating PolypeptideSensory Receptor CellsADCYAP1 protein, humanPituitary Adenylate Cyclase-Activating PolypeptideADCYAP1carpal tunnel syndromenerve regenerationperipheral nerve injurypituitary adenylate cyclase-activating peptide

Identifiers

PMID32651949
PMCPMC7462094
OpenAlexW3030793585

What Socratic 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 Socratic graph.