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dc.creatorGrammatikopoulou M.G., Gkiouras K., Markaki A.G., Gkouskou K.K., Aivaliotis M., Stylianou K., Bogdanos D.P.en
dc.date.accessioned2023-01-31T07:44:32Z
dc.date.available2023-01-31T07:44:32Z
dc.date.issued2020
dc.identifier10.1007/s42000-020-00199-6
dc.identifier.issn11093099
dc.identifier.urihttp://hdl.handle.net/11615/72711
dc.description.abstractPurpose: The salivary amylase gene (AMY1) copy number variation (CNV) is increased as a human adaptation to starch-enriched nutritional patterns. The purpose of this study was to evaluate the relationship between AMY1 CNV, dietary starch consumption, and anthropometric indices among a known population with elevated cardiovascular risk, being end-stage renal disease (ESRD) patients. Methods: A total of 43 ESRD patients were recruited based on the following inclusion criteria: being (1) adults, (2) on hemodialysis for more than 3 months, (3) able to communicate effectively, and (4) willing to participate. Anthropometric measurements were performed, dietary intake was recorded via food-frequency questionnaires, and AMY1 CNV was quantified in blood samples DNA via real-time PCR. Results: Median AMY1 CNV was 4.0 (2.0–17.0). A total of 21 patients had an even, and 22 had an odd AMY1 copy number (CN). Independent samples t tests revealed that AMY1-odd diploid CN is associated with increased body weight, waist and hip circumferences, and fat mass compared to the respective even diploid CN carrier group. No differences were observed for BMI or nutritional intake. Multiple regression analysis revealed that AMY1-odd diploid CN was positively associated with increased hip circumference (ß = 7.87, 95% CI = 0.34 to 15.39) and absolute fat mass (ß = 6.66, 95% CI = 0.98 to 12.34); however, after applying the Bonferroni correction for multiplicity, all regression analyses lost their significance. Conclusions: AMY1-odd diploid CN appears to be associated with selected adiposity variables among hemodialysis patients. However, more research is needed to verify this finding in this population with known increased cardiovascular risk. © 2020, Hellenic Endocrine Society.en
dc.language.isoenen
dc.sourceHormonesen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85084985011&doi=10.1007%2fs42000-020-00199-6&partnerID=40&md5=81e0f77b067a2abd43fd629665b181ff
dc.subjectstarchen
dc.subjectalpha amylase saliva isoenzymeen
dc.subjectAMY1A protein, humanen
dc.subjectadulten
dc.subjectageden
dc.subjectAMY1 geneen
dc.subjectanthropometric parametersen
dc.subjectArticleen
dc.subjectblood levelen
dc.subjectbody compositionen
dc.subjectbody weighten
dc.subjectBonferroni correctionen
dc.subjectcarbohydrate intakeen
dc.subjectcardiovascular risken
dc.subjectCaucasianen
dc.subjectclinical articleen
dc.subjectcontrolled studyen
dc.subjectdietary intakeen
dc.subjectdiploidyen
dc.subjectdisease associationen
dc.subjectDNA determinationen
dc.subjectend stage renal diseaseen
dc.subjectfat massen
dc.subjectfemaleen
dc.subjectfood frequency questionnaireen
dc.subjectgeneen
dc.subjectgenetic analysisen
dc.subjectgenetic associationen
dc.subjecthemodialysisen
dc.subjectheterozygoteen
dc.subjecthip circumferenceen
dc.subjecthumanen
dc.subjectmaleen
dc.subjectmultiple regressionen
dc.subjectnutritional assessmenten
dc.subjectobesityen
dc.subjectreal time polymerase chain reactionen
dc.subjectregression analysisen
dc.subjectStudent t testen
dc.subjecttreatment durationen
dc.subjectwaist circumferenceen
dc.subjectadipose tissueen
dc.subjectchronic kidney failureen
dc.subjectcopy number variationen
dc.subjectdiploidyen
dc.subjecteatingen
dc.subjectgeneticsen
dc.subjectmiddle ageden
dc.subjectmorphometryen
dc.subjectAdipose Tissueen
dc.subjectAdulten
dc.subjectBody Weights and Measuresen
dc.subjectDiploidyen
dc.subjectDNA Copy Number Variationsen
dc.subjectEatingen
dc.subjectFemaleen
dc.subjectHumansen
dc.subjectKidney Failure, Chronicen
dc.subjectMaleen
dc.subjectMiddle Ageden
dc.subjectRenal Dialysisen
dc.subjectSalivary alpha-Amylasesen
dc.subjectStarchen
dc.subjectSpringeren
dc.titleAMY1 diploid copy number among end-stage renal disease patientsen
dc.typejournalArticleen


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