Correlational studies on insulin resistance and leptin gene polymorphisms in peritoneal dialysis patients

Publish Year: 1394
نوع سند: مقاله ژورنالی
زبان: English
View: 123

This Paper With 9 Page And PDF Format Ready To Download

  • Certificate
  • من نویسنده این مقاله هستم

این Paper در بخشهای موضوعی زیر دسته بندی شده است:

استخراج به نرم افزارهای پژوهشی:

لینک ثابت به این Paper:

شناسه ملی سند علمی:

JR_IJBMS-18-9_006

تاریخ نمایه سازی: 3 آبان 1400

Abstract:

Objective(s):The aim of the study was to investigate the relationship between insulin resistance (IR) and leptin (LEP) gene polymorphisms in peritoneal dialysis (PD) patients. Materials and Methods: From July ۱, ۲۰۱۱ to August ۱, ۲۰۱۱, patients who received chronic PD were chosen and divided into three groups (DM, high HOMR-IR, and low HOMR-IR). Two PCR products of LEP were sequenced and aligned and the distribution of polymorphisms was analyzed using χ۲ analysis. In addition, serum leptin level, PD conditions, and biochemical parameters according to different genotype of G-۲۵۴۸A and A۱۹G were statistically analyzed (P-value<۰.۰۵). The relationship between LEP gene polymorphisms and prognosis was explored. Results: Totally ۱۵۷ patients with average age of ۵۵±۱۵ years old were chosen. Distribution of genotype frequencies was complied with Hardy-Weinberg equilibrium. Leptin level and BMI (body mass index) of the GG genotype of G-۲۵۴۸A were higher than that of GA or AA. The fasting glucose, cholesterol, etc. of AA genotype were lower, and the nPCR was higher than the two other genotypes. Serum leptin level and BMI of AA genotype of A۱۹G was higher than GA and GG genotypes; meanwhile, fasting blood glucose of that genotypes was the highest. In addition, survival rate of AA group of A۱۹G was very low. Conclusion:The G-۲۵۴۸A and A۱۹G polymorphisms were correlated with serum leptin level and IR. Leptin A۱۹G polymorphism may be prognostic for PD patients. This study may facilitate early intervention for IR in PD patients.

Authors

Liou Cao

Department of Nephrology, Molecular Cell Laboratory for Kidney Disease, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai Center for Peritoneal Dialysis Research, Shanghai, China

Shan Mou

Department of Nephrology, Molecular Cell Laboratory for Kidney Disease, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai Center for Peritoneal Dialysis Research, Shanghai, China

Wei Fang

Department of Nephrology, Molecular Cell Laboratory for Kidney Disease, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai Center for Peritoneal Dialysis Research, Shanghai, China

Chaojun Qi

Department of Nephrology, Molecular Cell Laboratory for Kidney Disease, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai Center for Peritoneal Dialysis Research, Shanghai, China

Xinbei Chang

Department of Nephrology, Molecular Cell Laboratory for Kidney Disease, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai Center for Peritoneal Dialysis Research, Shanghai, China

Leyi Gu

Department of Nephrology, Molecular Cell Laboratory for Kidney Disease, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai Center for Peritoneal Dialysis Research, Shanghai, China

Jiaqi Qian

Department of Nephrology, Molecular Cell Laboratory for Kidney Disease, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai Center for Peritoneal Dialysis Research, Shanghai, China

Zhaohui Ni

Department of Nephrology, Molecular Cell Laboratory for Kidney Disease, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai Center for Peritoneal Dialysis Research, Shanghai, China

مراجع و منابع این Paper:

لیست زیر مراجع و منابع استفاده شده در این Paper را نمایش می دهد. این مراجع به صورت کاملا ماشینی و بر اساس هوش مصنوعی استخراج شده اند و لذا ممکن است دارای اشکالاتی باشند که به مرور زمان دقت استخراج این محتوا افزایش می یابد. مراجعی که مقالات مربوط به آنها در سیویلیکا نمایه شده و پیدا شده اند، به خود Paper لینک شده اند :
  • Isse N, Ogawa Y, Tamura N, Masuzaki H, Mori K, ...
  • de Luis DA, Aller R, Izaola O, Conde R, Bouza ...
  • Ovsyannikova IG, White SJ, Larrabee BR, Grill DE, Jacobson RM, ...
  • Kohan L, Nasiri M, Habib A, Bolhasani A. Association of ...
  • Ribeiro R, Vasconcelos A, Costa S, Pinto D, Morais A, ...
  • Hager J, Clement K, Francke S, Dina C, Raison J, ...
  • Ohshiro Y, Ueda K, Nishi M, Ishigame M, Wakasaki H, ...
  • Lakka TA, Rankinen T, Weisnagel SJ, Chagnon YC, Lakka H-M, ...
  • Mammes O, Betoulle D, Aubert R, Herbeth B, Siest G, ...
  • Van der Lende T, Te Pas M, Veerkamp R, Liefers ...
  • Montague CT, Farooqi IS, Whitehead JP, Soos MA, Rau H, ...
  • Le Stunff C, Le Bihan C, Schork NJ, Bougnères P. A ...
  • Ren W, Zhang S-H, Wu J, Ni Y-X. Polymorphism of ...
  • Simpson S, Raubenheimer D. The protein leverage hypothesis in human ...
  • Cao L, Mou S, Fang W, Gu L, Huang J, ...
  • Gawkrodger D, Ferguson A, Barnetson R. Nutritional status in patients ...
  • Mazen I, El-Gammal M, Abdel-Hamid M, Amr K. A novel ...
  • Lönnqvist F, Arner P, Nordfors L, Schalling M. Overexpression of ...
  • Zhang Y, Proenca R, Maffei M, Barone M, Leopold L, ...
  • Considine RV, Considine EL, Williams C, Nyce MR, Magosin SA, ...
  • Hinuy HM, Hirata MH, Forti N, Diament J, Sampaio MF, ...
  • Ma D, Feitosa MF, Wilk JB, Laramie JM, Yu K, ...
  • نمایش کامل مراجع