Evidence map›Paper›PMID 37933884›Full record

Observational studyEuropean journal of neurology2024

Ultrasonic detection of vagus, accessory, and phrenic nerve atrophy in amyotrophic lateral sclerosis: Relation to impairment and mortality.

Uwe Walter, Gretlies Sobiella, Johannes Prudlo, Michael Batchakaschvili, Jan Böhmert, Alexander Storch, Andreas Hermann

Open access · hybridAbstract readObservational Study
In one paragraph

Observational study in European journal of neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 10% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Article
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  4. Article
  5. Review
  6. Article
  7. Article
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  9. Observational
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.

Uwe WalterDepartment of Neurology, Rostock University Medical Center, Rostock, Germany.ORCID 0000-0002-6280-785X
Gretlies SobiellaDepartment of Neurology, Rostock University Medical Center, Rostock, Germany.
Johannes PrudloDepartment of Neurology, Rostock University Medical Center, Rostock, Germany.
Michael BatchakaschviliDepartment of Neurology, Rostock University Medical Center, Rostock, Germany.
Jan BöhmertDepartment of Neurology, Rostock University Medical Center, Rostock, Germany.
Alexander StorchDepartment of Neurology, Rostock University Medical Center, Rostock, Germany.ORCID 0000-0002-1133-9216
Andreas HermannDeutsches Zentrum für Neurodegenerative Erkrankungen Rostock/Greifswald, Rostock, Germany.
German Center for Neurodegenerative Diseases · DEUniversity of Rostock · DE

Funding

European Regional Development Fund GHS-15-0017Hermann und Lilly Schilling-Stiftung für Medizinische Forschung
6 · The paper itself

Abstract

background and purposeIn amyotrophic lateral sclerosis (ALS), phrenic nerve (PN) atrophy has been found, whereas there is controversy regarding vagus nerve (VN) atrophy. Here, we aimed to find out whether PN atrophy is related to respiratory function and 12-month survival. Moreover, we investigated the relevance of VN and spinal accessory nerve (AN) atrophy in ALS.

methodsThis prospective observational monocentric study included 80 adult participants (40 ALS patients, 40 age- and sex-matched controls). The cross-sectional area (CSA) of bilateral cervical VN, AN, and PN was measured on high-resolution ultrasonography. Clinical assessments included the Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised (ALSFRS-R), the Non-Motor Symptoms Questionnaire, and handheld spirometry of forced vital capacity (FVC). One-year survival was documented.

resultsThe CSA of each nerve, VN, AN, and PN, was smaller in ALS patients compared to controls. VN atrophy was unrelated to nonmotor symptom scores. PN CSA correlated with the respiratory subscore of the ALSFRS-R (Spearman test, r = 0.59, p < 0.001), the supine FVC (r = 0.71, p < 0.001), and the relative change of sitting-supine FVC (r = -0.64, p = 0.001). Respiratory impairment was predicted by bilateral mean PN CSA (p = 0.046, optimum cutoff value of ≤0.37 mm

conclusionsUltrasonography detects degeneration of cranial nerve motor fibers. PN and AN calibers are tightly related to respiratory function and 1-year survival in ALS.

Indexed as

Amyotrophic Lateral SclerosisAdultAtrophyFemaleHumansMalePhrenic NerveUltrasonicsVagus Nerveaccessory nerveamyotrophic lateral sclerosismotor neuron diseasenerve ultrasoundphrenic nerverespiratory functionvagus nerve

Identifiers

PMID37933884
PMCPMC11235926
OpenAlexW4388454454

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.