AMY1 diploid copy number among end-stage renal disease patients

被引:2
作者
Grammatikopoulou, Maria G. [1 ]
Gkiouras, Konstantinos [1 ]
Markaki, Anastasia G. [2 ]
Gkouskou, Kalliopi K. [3 ,4 ]
Aivaliotis, Michalis [5 ,6 ]
Stylianou, Konstantinos [7 ]
Bogdanos, Dimitrios P. [1 ,8 ]
机构
[1] Univ Thessaly, Fac Med, Sch Hlth Sci, Dept Rheumatol & Clin Immunol, Larisa, Greece
[2] Hellen Mediterranean Univ, Fac Hlth Sci, Dept Nutr & Dietet, Sitia, Greece
[3] Univ West Attica, Fac Hlth & Caring Profess, Dept Med Labs, Athens, Greece
[4] Biol Res Co, Embiodiagnost, Melissinon & Damvergidon Str, Iraklion, Crete, Greece
[5] Aristotle Univ Thessaloniki, Fac Hlth Sci, Dept Med, Lab Biol Chem, Thessaloniki, Greece
[6] Fdn Res & Technol Hellas FORTH, Inst Mol Biol & Biotechnol, Iraklion, Crete, Greece
[7] Univ Hosp Heraklion, Dept Nephrol, Iraklion, Crete, Greece
[8] Kings Coll London, MRC Ctr Transplantat, Div Transplantat Immunol & Mucosal Biol, Med Sch, London, England
来源
HORMONES-INTERNATIONAL JOURNAL OF ENDOCRINOLOGY AND METABOLISM | 2020年 / 19卷 / 03期
关键词
Chronic kidney disease; Hemodialysis patients; Salivary amylase gene; Nutrigenetics; Starch; Nutrition transition; Metabolism; Obesity; SALIVARY AMYLASE GENE; KIDNEY-DISEASE; OBESITY; RISK; ADIPONECTIN; NUTRITION; MORTALITY; ASSOCIATE; DIET; CKD;
D O I
10.1007/s42000-020-00199-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose 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.
引用
收藏
页码:369 / 376
页数:8
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