Evidence map›Paper›PMID 26078981›Full record

Observational studyJournal of immunology research2015

Achalasia--An Autoimmune Inflammatory Disease: A Cross-Sectional Study.

J Furuzawa-Carballeda, D Aguilar-León, A Gamboa-Domínguez, M A Valdovinos, C Nuñez-Álvarez, L A Martín-del-Campo, A B Enríquez, E Coss-Adame, A E Svarch, A Flores-Nájera and 3 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Journal of immunology research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 1 pooled it
4.2field-weighted citation impact, top 6% 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

52 citing papers in PubMed, 1 synthesis or guideline pooled it, 117 citations in OpenAlex.

  1. Pooled it
  2. Nutrition in achalasia cardia-A neglected frontier.Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Two onset types of achalasia and the long-term course to diagnosis.Esophagus : official journal of the Japan Esophageal Society · 2024
    Article
  13. Review
  14. Article
  15. Article
  16. Altered Esophageal Smooth Muscle Phenotype in Achalasia.Journal of neurogastroenterology and motility · 2024
    Article
  17. Article
  18. Article
  19. Modern Achalasia: Diagnosis, Classification, and Treatment.Journal of neurogastroenterology and motility · 2023
    Review
  20. Article
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

13 authors.

J Furuzawa-CarballedaDepartment of Immunology and Rheumatology, National Institute of Medical Sciences and Nutrition, Vasco de Quiroga No. 15, Colonia Sección XVI, 14000 Mexico City, DF, Mexico.
D Aguilar-LeónDepartment of Pathology, National Institute of Medical Sciences and Nutrition, Vasco de Quiroga No. 15, Colonia Sección XVI, 14000 Mexico City, DF, Mexico.
A Gamboa-DomínguezDepartment of Pathology, National Institute of Medical Sciences and Nutrition, Vasco de Quiroga No. 15, Colonia Sección XVI, 14000 Mexico City, DF, Mexico.
M A ValdovinosDepartment of Gastroenterology, National Institute of Medical Sciences and Nutrition, Vasco de Quiroga No. 15, Colonia Sección XVI, 14000 Mexico City, DF, Mexico.
C Nuñez-ÁlvarezDepartment of Immunology and Rheumatology, National Institute of Medical Sciences and Nutrition, Vasco de Quiroga No. 15, Colonia Sección XVI, 14000 Mexico City, DF, Mexico.
L A Martín-del-CampoDepartment of Experimental Surgery, National Institute of Medical Sciences and Nutrition, Vasco de Quiroga No. 15, Colonia Sección XVI, 14000 Mexico City, DF, Mexico.
A B EnríquezDepartment of Immunology and Rheumatology, National Institute of Medical Sciences and Nutrition, Vasco de Quiroga No. 15, Colonia Sección XVI, 14000 Mexico City, DF, Mexico.
E Coss-AdameDepartment of Gastroenterology, National Institute of Medical Sciences and Nutrition, Vasco de Quiroga No. 15, Colonia Sección XVI, 14000 Mexico City, DF, Mexico.
A E SvarchDepartment of Experimental Surgery, National Institute of Medical Sciences and Nutrition, Vasco de Quiroga No. 15, Colonia Sección XVI, 14000 Mexico City, DF, Mexico.
A Flores-NájeraDepartment of Experimental Surgery, National Institute of Medical Sciences and Nutrition, Vasco de Quiroga No. 15, Colonia Sección XVI, 14000 Mexico City, DF, Mexico.
A Villa-BañosDepartment of Experimental Surgery, National Institute of Medical Sciences and Nutrition, Vasco de Quiroga No. 15, Colonia Sección XVI, 14000 Mexico City, DF, Mexico.
J C CeballosDepartment of Experimental Surgery, National Institute of Medical Sciences and Nutrition, Vasco de Quiroga No. 15, Colonia Sección XVI, 14000 Mexico City, DF, Mexico.
G Torres-VillalobosDepartment of Experimental Surgery, National Institute of Medical Sciences and Nutrition, Vasco de Quiroga No. 15, Colonia Sección XVI, 14000 Mexico City, DF, Mexico.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Idiopathic achalasia is a disease of unknown etiology. The loss of myenteric plexus associated with inflammatory infiltrates and autoantibodies support the hypothesis of an autoimmune mechanism. Thirty-two patients diagnosed by high-resolution manometry with achalasia were included. Twenty-six specimens from lower esophageal sphincter muscle were compared with 5 esophagectomy biopsies (control). Immunohistochemical (biopsies) and flow cytometry (peripheral blood) analyses were performed. Circulating anti-myenteric autoantibodies were evaluated by indirect immunofluorescence. Herpes simplex virus-1 (HSV-1) infection was determined by in situ hybridization, RT-PCR, and immunohistochemistry. Histopathological analysis showed capillaritis (51%), plexitis (23%), nerve hypertrophy (16%), venulitis (7%), and fibrosis (3%). Achalasia tissue exhibited an increase in the expression of proteins involved in extracellular matrix turnover, apoptosis, proinflammatory and profibrogenic cytokines, and Tregs and Bregs versus controls (P < 0.001). Circulating Th22/Th17/Th2/Th1 percentage showed a significant increase versus healthy donors (P < 0.01). Type III achalasia patients exhibited the highest inflammatory response versus types I and II. Prevalence of both anti-myenteric antibodies and HSV-1 infection in achalasia patients was 100% versus 0% in controls. Our results suggest that achalasia is a disease with an important local and systemic inflammatory autoimmune component, associated with the presence of specific anti-myenteric autoantibodies, as well as HSV-1 infection.

Indexed as

AdultAgedAutoantibodiesAutoimmune DiseasesCase-Control StudiesCross-Sectional StudiesEsophageal AchalasiaFemaleFluorescent Antibody Technique, IndirectHerpes SimplexHerpesvirus 1, HumanHumansImmunohistochemistryInflammationMaleMiddle AgedAutoantibodies

Identifiers

PMID26078981
PMCPMC4452860
OpenAlexW1548391375

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.