Evidence map›Paper›PMID 32390518›Full record

ArticleBiological research for nursing2020

Genetic Variation Near chrXq22-q23 Is Linked to Emotional Functioning in Cystic Fibrosis.

Eric Barbato, Barbara Daly, Sara Douglas, Mary Kerr, Paul Litman, Rebecca Darrah

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Article in Biological research for nursing, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Eric BarbatoDepartment of Genetics and Genome Sciences, Case Western Reserve University, Cleveland, OH, USA.ORCID 0000-0001-8132-0679
Barbara DalyFrances Payne Bolton School of Nursing, Case Western Reserve University, Cleveland, OH, USA.
Sara DouglasFrances Payne Bolton School of Nursing, Case Western Reserve University, Cleveland, OH, USA.
Mary KerrFrances Payne Bolton School of Nursing, Case Western Reserve University, Cleveland, OH, USA.
Paul LitmanFrances Payne Bolton School of Nursing, Case Western Reserve University, Cleveland, OH, USA.
Rebecca DarrahDepartment of Genetics and Genome Sciences, Case Western Reserve University, Cleveland, OH, USA.

Funding

Genetic Modifiers of Health Related Quality of Life in Cystic FibrosisF31NR017341 · NINR · CASE WESTERN RESERVE UNIVERSITY · PI BARBATO, ERIC · 2018 to 2019
$67k
NINR NIH HHS F31 NR017341
6 · The paper itself

Abstract

introductionCystic fibrosis (CF) is an autosomal recessive disease that affects many organ systems, most notably the pulmonary and gastrointestinal systems. Through genome-wide association studies, multiple genetic regions modifying CF-related pulmonary and gastrointestinal symptoms have been identified, but translation of these findings to clinical benefit remains elusive. Symptom variation in CF patients has been associated with changes in health-related quality of life (HRQOL), but the relationship between CF symptom-modifying genetic loci and HRQOL has not been explored. The purpose of this study was to determine whether two previously identified genetic modifiers of CF-related pathology also modify the subscales of HRQOL.

methodsHRQOL and genotype data were obtained and analyzed. Linear regressions were used to examine the amount of variance in HRQOL subscales that could be explained by genotype for each modifier locus.

resultsA significant regression equation was found between genotype for rs5952223, a variant near chrXq22-q23, and emotional functioning in a sample of 129 CF patients. DISCUSSION: These data suggest that genotype for this single-nucleotide polymorphism is associated with emotional functioning in CF patients and highlight this genetic region as a potential therapeutic target, irrespective of CF transmembrane conductance regulator genotype.

Indexed as

EmotionsGenotypeAdultCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorFemaleGenetic VariationGenome-Wide Association StudyHumansMaleMiddle AgedOhioPolymorphism, Single NucleotideCFTR protein, humanCystic Fibrosis Transmembrane Conductance Regulatorcystic fibrosisgenetic modifiergeneticshealth-related quality of lifepediatrics

Identifiers

PMID32390518
PMCPMC7492775

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