Publicacion


Titulo: Heritability and genetic correlation between GERD symptoms severity, metabolic syndrome, and inflammation markers in families living in Mexico City
Autores: REDING-BERNAL A
SANCHEZ-PEDRAZA V
MORENO-MACIAS H
SOBRINO-COSSIO S
MARÍA ELIZABETH TEJERO BARRERA
BURGUETE-GARCIA AI
LEON-HERNANDEZ M
SERRATOS-CANALES MF
DUGGIRALA R
LOPEZ-ALVARENGA JC
Tipo de Licencia: http://creativecommons.org/licenses/by/4.0
Fecha de Publicación: 5 de Junio de 2017
Resumen: OBJECTIVE: The aim of this study was to estimate the heritability (h2) and genetic correlation (rhoG) between GERD symptoms severity, metabolic syndrome components, and inflammation markers in Mexican families. METHODS: Cross-sectional study which included 32 extended families resident in Mexico City. GERD symptoms severity was assessed by the ReQuest in Practice questionnaire. Heritability and genetic correlation were determined using the Sequential Oligogenic Linkage Analysis Routines software. RESULTS: 585 subjects were included, the mean age was 42 (+/-16.7) years, 57% were women. The heritability of the severity of some GERD symptoms was h2 = 0.27, 0.27, 0.37, and 0.34 (p-value <1.0x10-5) for acidity complaints, lower abdominal complaints, sleep disturbances, and total ReQuest score, respectively. Heritability of metabolic syndrome components ranged from 0.40 for fasting plasma glucose to 0.61 for body mass index and diabetes mellitus. The heritability for fibrinogen and C-reactive protein was 0.64 and 0.38, respectively. Statistically significant genetic correlations were found between acidity complaints and fasting plasma glucose (rhoG = 0.40); sleep disturbances and fasting plasma glucose (rhoG = 0.36); acidity complaints and diabetes mellitus (rhoG = 0.49) and between total ReQuest score and fasting plasma glucose (rhoG = 0.43). The rest of metabolic syndrome components did not correlate with GERD symptoms. CONCLUSION: Genetic factors substantially explain the phenotypic variance of the severity of some GERD symptoms, metabolic syndrome components and inflammation markers. Observed genetic correlations suggest that these phenotypes share common genes. These findings suggest conducting further investigation, as the determination of a linkage analysis in order to identify regions of susceptibility for developing of GERD and metabolic syndrome.
Editorial: PLoS One
Idioma: Ingles
Palabras Clave: Adult
Blood Glucose/metabolism
Body Mass Index
C-Reactive Protein/metabolism
Cross-Sectional Studies
Fasting
Female
Fibrinogen/metabolism
Gastroesophageal Reflux/complications/diagnosis/epidemiology/*genetics
*Heredity
Humans
Inflammation
Male
Metabolic Syndrome/complications/diagnosis/epidemiology/*genetics
Mexico/epidemiology
Middle Aged
Severity of Illness Index
Sleep Initiation and Maintenance Disorders/complications/diagnosis/epidemiology/*genetics
Surveys and Questionnaires
URL: https://repositorio.inmegen.gob.mx/record/36
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