Evidence map›Paper›PMID 29438387›Full record

ArticlePloS one2018

Genetic association study of NLRP1, CARD, and CASP1 inflammasome genes with chronic Chagas cardiomyopathy among Trypanosoma cruzi seropositive patients in Bolivia.

Steven J Clipman, Josephine Henderson-Frost, Katherine Y Fu, Caryn Bern, Jorge Flores, Robert H Gilman

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

10 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Caspase-1 Variants and Plasma IL-1β in Patients withInternational journal of molecular sciences · 2024
    Article
  5. Review
  6. Review
  7. Inflammasome genetics and complex diseases: a comprehensive review.European journal of human genetics : EJHG · 2020
    Review
  8. Review
  9. Article
  10. Review
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

6 authors at 5 institutions in 2 countries.

Steven J ClipmanDepartment of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, United States of America.ORCID 0000-0002-2366-8420
Josephine Henderson-FrostMassachusetts General Hospital, Boston, Massachusetts, United States of America.
Katherine Y FuUniversity of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, United States of America.
Caryn BernDepartment of Epidemiology and Biostatistics, University of California San Francisco School of Medicine, San Francisco, California, United States of America.
Jorge FloresHospital San Juan de Dios, Santa Cruz de la Sierra, Bolivia.
Robert H GilmanDepartment of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, United States of America.
Johns Hopkins University · USMassachusetts General Hospital · USUniversidad Privada de Santa Cruz de la Sierra · BOUniversity of California, San Francisco · USUniversity of Pittsburgh Medical Center · US

Funding

Predictors of cardiomyopathy progression in a Chagas disease cohort in BoliviaR01AI107028 · NIAID · JOHNS HOPKINS UNIVERSITY · PI GILMAN, ROBERT H · 2014 to 2023
$6.6M
NIAID NIH HHS R01 AI107028NIH HHS 5R01AI107028-04
6 · The paper itself

Abstract

About 20-30% of people infected with Chagas disease present with chronic Chagas cardiomyopathy (CCC), the most serious and frequent manifestation of the disease, while others remain asymptomatic and often do not experience Chagas-specific mortality. It is not currently well understood what causes these differential disease outcomes, but a genetic predisposition within the host could play an important role. This study examined variants in the NLRP1, CARD, and CASP1 inflammasome genes among 62 T. cruzi seropositive patients from Bolivia (38 cases with CCC and 24 asymptomatic controls) to uncover associations with CCC. All subjects underwent a complete medical examination including electrocardiogram (EKG) and echocardiogram. After genotype calling and quality control filtering with exclusion of 3 cases and 3 controls, association analysis was performed across 76 directly genotyped SNPs in NLRP1, CARD, and CASP1 genes, adjusting for age, sex, and population stratification. One SNP (rs11651270; Bonferroni-corrected p = 0.036) corresponding to a missense mutation in NLPR1 was found to be significant after adjustment for multiple testing, and a suggestive association was seen in CARD11 (rs6953573; Bonferroni-corrected p = 0.060). Although limited by sample size, the study results suggest variations in the inflammasome, particularly in NLRP1 and CARD11, may be associated with CCC.

Indexed as

Genome-Wide Association StudyAdaptor Proteins, Signal TransducingAdultApoptosis Regulatory ProteinsBoliviaCARD Signaling Adaptor ProteinsCase-Control StudiesCaspase 1Chagas CardiomyopathyChronic DiseaseFemaleGuanylate CyclaseHumansInflammasomesMaleMiddle AgedAdaptor Proteins, Signal TransducingApoptosis Regulatory ProteinsCARD11 protein, humanCARD Signaling Adaptor ProteinsCaspase 1Guanylate CyclaseInflammasomesNLRP1 protein, humanNLR Proteins

Identifiers

PMID29438387
PMCPMC5810984
OpenAlexW2792222277

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.