Evidence map›Paper›PMID 33114181›Full record

ArticleJournal of clinical medicine2020

Deciphering the Genetics of Primary Angioedema with Normal Levels of C1 Inhibitor.

Gedeon Loules, Faidra Parsopoulou, Maria Zamanakou, Dorottya Csuka, Maria Bova, Teresa González-Quevedo, Fotis Psarros, Gregor Porebski, Matthaios Speletas, Davide Firinu and 7 more

Abstract read
In one paragraph

Article in Journal of clinical medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
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

21 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Hereditary angioedema with normal C1 inhibitor associated with carboxypeptidase N deficiency.The journal of allergy and clinical immunology. Global · 2024
    Article
  11. Hereditary or acquired? Comprehensive genetic testing assists in stratifying angioedema patients.Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology · 2024
    Article
  12. Review
  13. Genetic Variants Leading to Urticaria and Angioedema and Associated Biomarkers.The journal of allergy and clinical immunology. In practice · 2023
    Article
  14. Review
  15. Article
  16. Frontiers in allergy · 2022
    Review
  17. Article
  18. Review
  19. The Genetics of Hereditary Angioedema: A Review.Journal of clinical medicine · 2021
    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

17 authors.

Gedeon LoulesCeMIA SA, Makriyianni 31, GR-41334 Larissa, Greece.
Faidra ParsopoulouCeMIA SA, Makriyianni 31, GR-41334 Larissa, Greece.
Maria ZamanakouCeMIA SA, Makriyianni 31, GR-41334 Larissa, Greece.
Dorottya CsukaHungarian Angioedema Center, 3rd Department of Internal Medicine, Semmelweis University, Kutvolgyi ut 4, H-1125 Budapest, Hungary.ORCID 0000-0003-3610-9852
Maria BovaDepartment of Translational Medicine, University of Naples, Via S. Pansini 5, 80131 Naples, Italy.ORCID 0000-0002-7655-0696
Teresa González-QuevedoReference Unit for Angioedema in Andalusia, Allergy Department, Virgen del Rocío University Hospital, Av Manuel Siurot s/n, 41013 Seville, Spain.ORCID 0000-0002-0866-9134
Fotis PsarrosDepartment of Allergology, Navy Hospital, Deinokratous 70, GR-11521 Athens, Greece.ORCID 0000-0001-9810-3275
Gregor PorebskiDepartment of Clinical and Environmental Allergology, Jagiellonian University Medical College, Sniadeckich 10, 31-531 Krakow, Poland.ORCID 0000-0002-6146-0188
Matthaios SpeletasDepartment of Immunology & Histocompatibility, School of Health Sciences, Faculty of Medicine, University of Thessaly, Panepistimiou 3, GR-41500 Biopolis, Larissa, Greece.
Davide FirinuDepartment of Medical Sciences and Public Health, University of Cagliari, 09042 Monserrato, Italy.ORCID 0000-0002-5768-391X
Stefano Del GiaccoDepartment of Medical Sciences and Public Health, University of Cagliari, 09042 Monserrato, Italy.
Chiara SuffrittiDepartment of Biomedical and Clinical Sciences Luigi Sacco, University of Milan, Via G.B. Grassi 74, 20157 Milan, Italy.
Michael MakrisAllergy Unit, 2nd Department of Dermatology and Venereology, National and Kapodistrian University of Athens, University Hospital "Attikon", Rimini 1, GR-12462 Chaidari, Athens, Greece.
Sofia VatsiouCeMIA SA, Makriyianni 31, GR-41334 Larissa, Greece.
Andrea ZanichelliDepartment of Biomedical and Clinical Sciences Luigi Sacco, University of Milan, Via G.B. Grassi 74, 20157 Milan, Italy.
Henriette FarkasHungarian Angioedema Center, 3rd Department of Internal Medicine, Semmelweis University, Kutvolgyi ut 4, H-1125 Budapest, Hungary.
Anastasios E GermenisCeMIA SA, Makriyianni 31, GR-41334 Larissa, Greece.ORCID 0000-0002-3315-6947

Funding

Shire International GmbH, a member of the Takeda group of companies IIR-GRC-000905
6 · The paper itself

Abstract

The genetic alteration underlying the great majority of primary angioedema with normal C1 inhibitor (nl-C1-INH-HAE) cases remains unknown. To search for variants associated with nl-C1-INH-HAE, we genotyped 133 unrelated nl-C1-INH-HAE patients using a custom next-generation sequencing platform targeting 55 genes possibly involved in angioedema pathogenesis. Patients already diagnosed with

Indexed as

next-generation sequencingpedigree analysisprimary angioedemaprimary angioedema with normal C1 inhibitor

Identifiers

PMID33114181
PMCPMC7690775

What OpenQuestion holds

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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.