Evidence map›Paper›PMID 32193469›Full record

SynthesisScientific reports2020

Genetic polymorphisms of IL17A associated with Chagas disease: results from a meta-analysis in Latin American populations.

Mariana Strauss, Miriam Palma-Vega, Desiré Casares-Marfil, Pau Bosch-Nicolau, María Silvina Lo Presti, Israel Molina, Clara Isabel González, Chagas Genetics CYTED Network, Javier Martín, Marialbert Acosta-Herrera

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. The IL-17 family in diseases: from bench to bedside.Signal transduction and targeted therapy · 2023
    Review
  5. Review
  6. Article
  7. 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

10 authors at 10 institutions in 7 countries.

Mariana StraussCentro de Estudios e Investigación de la Enfermedad de Chagas y Leishmaniasis, FCM, INICSA-CONICET-UNC, Córdoba, Argentina. marianastr86@gmail.com.
Miriam Palma-VegaInstituto de Parasitología y Biomedicina López-Neyra, IPBLN-CSIC, Granada, España.
Desiré Casares-MarfilInstituto de Parasitología y Biomedicina López-Neyra, IPBLN-CSIC, Granada, España.
Pau Bosch-NicolauUnidad de Medicina Tropical y Salud Internacional Hospital Universitari Vall d'Hebron, PROSICS, Barcelona, España.
María Silvina Lo PrestiCentro de Estudios e Investigación de la Enfermedad de Chagas y Leishmaniasis, FCM, INICSA-CONICET-UNC, Córdoba, Argentina.
Israel MolinaUnidad de Medicina Tropical y Salud Internacional Hospital Universitari Vall d'Hebron, PROSICS, Barcelona, España.
Clara Isabel GonzálezGIEM, Universidad Industrial de Santander, Bucaramanga, Colombia.
Chagas Genetics CYTED Network
Javier MartínInstituto de Parasitología y Biomedicina López-Neyra, IPBLN-CSIC, Granada, España. javiermartin@ipb.csic.es.
Marialbert Acosta-HerreraInstituto de Parasitología y Biomedicina López-Neyra, IPBLN-CSIC, Granada, España. m.acostaherrera@ipb.csic.es.
Instituto de Parasitología y Biomedicina "López - Neyra" · ESInstituto de Investigaciones en Ciencias de la Salud · ARConsejo Nacional de Investigaciones Científicas y Técnicas · ARFundación Cardiovascular de Colombia · COInstituto Conmemorativo Gorgas de Estudios de la Salud · PAVall d'Hebron Hospital Universitari · ESBarcelona Institute for Global Health · ESCentro de Biología Molecular Severo Ochoa · ESIndustrial University of Santander · COInstituto Venezolano de Investigaciones Científicas · VE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic factors and the immunologic response have been suggested to determine the susceptibility against the infection and the outcome of Chagas disease. In the present study, we analysed three IL17A genetic variants (rs4711998, rs8193036 and rs2275913) regarding the predisposition to Trypanosoma cruzi infection and the development of chronic Chagas cardiomyopathy (CCC) in different Latin American populations. A total of 2,967 individuals from Colombia, Argentina, Bolivia and Brazil, were included in this study. The individuals were classified as seronegative and seropositive for T. cruzi antigens, and this last group were divided into asymptomatic and CCC. For T. cruzi infection susceptibility, the IL17A rs2275913*A showed a significant association in a fixed-effect meta-analysis after a Bonferroni correction (P = 0.016, OR = 1.21, 95%CI = 1.06-1.41). No evidence of association was detected when comparing CCC vs. asymptomatic patients. However, when CCC were compared with seronegative individuals, it showed a nominal association in the meta-analysis (P = 0.040, OR = 1.20, 95%CI = 1.01-1.45). For the IL17A rs4711998 and rs8193036, no association was observed. In conclusion, our results suggest that IL17A rs2275913 plays an important role in the susceptibility to T. cruzi infection and could also be implicated in the development of chronic cardiomyopathy in the studied Latin American population.

Indexed as

Chagas DiseaseGenetic Association StudiesGenetic Predisposition to DiseaseInterleukin-17Polymorphism, GeneticAdultAgedAged, 80 and overFemaleHumansLatin AmericaMaleMiddle AgedIL17A protein, humanInterleukin-17

Identifiers

PMID32193469
PMCPMC7081280
OpenAlexW3011418201

What OpenQuestion 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 OpenQuestion graph.