Evidence map›Paper›PMID 26258862›Full record

ArticlePediatric pulmonology2015

Changing incidence of cystic fibrosis in Wisconsin, USA.

Katelyn Parker-McGill, Melodee Nugent, Rachel Bersie, Gary Hoffman, Michael Rock, Mei Baker, Philip M Farrell, Pippa Simpson, Hara Levy

Abstract read
In one paragraph

Article in Pediatric pulmonology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Contemporary cystic fibrosis incidence rates in Canada and the United States.Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2023
    Article
  2. Article
  3. Review
  4. Article
  5. The future of cystic fibrosis care: a global perspective.The Lancet. Respiratory medicine · 2020
    Review
  6. Article
  7. Article
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Katelyn Parker-McGill *Children's Research Institute, Children's Hospital of Wisconsin, Milwaukee, Wisconsin.
Melodee Nugent *Children's Research Institute, Children's Hospital of Wisconsin, Milwaukee, Wisconsin.
Rachel BersieChildren's Research Institute, Children's Hospital of Wisconsin, Milwaukee, Wisconsin.
Gary HoffmanWisconsin State Lab of Hygiene, Madison, Wisconsin.
Michael RockPediatrics, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin.
Mei BakerWisconsin State Lab of Hygiene, Madison, Wisconsin.
Philip M FarrellPediatrics, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin.
Pippa SimpsonChildren's Research Institute, Children's Hospital of Wisconsin, Milwaukee, Wisconsin.
Hara LevyChildren's Research Institute, Children's Hospital of Wisconsin, Milwaukee, Wisconsin.

Funding

Integration of Genomics with Genetics - Molecular Phenotypes for CF Lung DiseaseDP2OD007031 · OD · MEDICAL COLLEGE OF WISCONSIN · PI LEVY, HARA · 2010 to 2010
$2.2M
NIH HHS DP2 OD007031NIH HHS DP2OD007031PHS HHS D.K. 34108
6 · The paper itself

Abstract

rationalePrevious investigations of cystic fibrosis (CF) incidence in Massachusetts, Colorado, and Minnesota (USA) yielded contradictory results, particularly regarding allele p.Phe508del; the racial compositions of the cohorts were not reported.

objectivesTo clarify discrepancies in reported incidence with the ultimate goal of improving screening and quality of care, we assessed CF incidence, stratified by race and mutations in cystic fibrosis transmembrane conductance regulator (CFTR), in Wisconsin (USA) from 1994 to 2011.

methodsData on patients diagnosed with CF (N = 283), CFTR genotypes, CF carriers, and birth rate were collected. All data were categorized by racial background of the birth mother and the incidence of CF births was accordingly adjusted. Spearman's nonparametric rank correlation and Fisher's exact test were performed for continuous and categorical variables, respectively. Trends over time were fitted with a cubic spline.

resultsWe detected a trending increase in CF cases (range within all data 1.67-2.98 per 10,000 births per year), homozygous p.Phe508del cases (0.57-1.79 per 10,000), heterozygous p.Phe508del cases (0.29-1.55 per 10,000), and cases lacking p.Phe508del (0-0.45 per 10,000). Both the number of cases lacking the p.Phe508del mutation per year and the number of cases lacking p.Phe508del per 10,000 births significantly increased (P = 0.05) from 1994 to 2011; the increase in overall incidence was not significant. The number of carriers identified through newborn screening significantly increased within the non-Hispanic Black (P = 0.0.021) and Hispanic (P = 0.003) populations.

conclusionThe racial composition of the CF cohort is changing in Wisconsin, possibly influencing disease detection, care, and outcome.

Indexed as

MutationAllelesCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorFemaleGenotypeHumansIncidenceInfant, NewbornMaleNeonatal ScreeningRetrospective StudiesWisconsinCystic Fibrosis Transmembrane Conductance RegulatorCFTR mutationepidemiologyincidence of CFTRrace

Identifiers

PMID26258862
PMCPMC4615551

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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.