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Epigenetik ve Böbrek Hastalıkları

Yıl 2020, Cilt: 3 Sayı: 3, 161 - 166, 30.09.2020

Öz

Epigenetik DNA diziliminde bir değişiklik olmadan gen ifadelenmesinde meydana gelen kalıtsal değişiklikler olarak tanımlanmaktadır. Bu konuda yapılan çalışmalar, çoğunlukla hastalıkların fetal orijinleri ile ilgilenmekte ve çevresel faktörlerin aracı olduğu rahim içi maruziyetlerin hastalıklar üzerindeki etkilerini araştırmaktadır. Son yıllarda böbrek hastalıkları ile ilişkili olarak yapılan epigenetik çalışma sayısı giderek artmakta ve beslenme şeklinin böbrek hastalıkları ile ilişkili epigenetik varyasyonları etkilediği bildirilmektedir. Bu çalışmalar maternal olarak yetersiz-aşırı beslenme veya gestasyonel diyabetin yavrunun böbrek fonksiyonları üzerine etkisine yoğunlaşmaktadır. Buna göre annenin beslenme şekli doğrudan veya dolaylı olarak yavrunun nefron sayısı, glomerulofiltrasyın hızı (GFR) ve renin-anjiotensin sistemini (RAS) değiştirmekte ve hem doğum sonrası erken dönemde hem de yaşamın ilerleyen yıllarında etkisini göstermektedir. Bu derlemede, maternal beslenme şeklinin yavrunun böbrek fonksiyonları ile bağlantılı epigenetik parametreler üzerine ilişkisinin incelenmesi amaçlanmıştır.

Destekleyen Kurum

yoktur.

Proje Numarası

yoktur.

Kaynakça

  • Alias NA, Aziz W, Amn WS, Mohamad C, Anuar C, Roslan R, Mohd Noor N. (2015). Effects of high and low maternal dietary sodium intake during pregnancy on the offsprings’ glomerular number in rats. 587 (11), 2635-2646.
  • Altunkaynak ME, Özbek E, Altunkaynak BZ, Can İ, Unal D, Unal B. (2008). The effects of high-fat diet on the renal structure and morphometric parametric of kidneys in rats. Journal of anatomy, 212(6), 845-852.
  • Armitage JA, Burke SL, Prior LJ, Barzel B, Eikelis N, Lim K, Head GA. (2012). Rapid onset of renal sympathetic nerve activation in rabbits fed a high-fat diet. Hypertension, 60,163–171.
  • Bahar A, Makhlough A, Yousefi A, Kashi Z, Abediankenari S. (2013). Correlation between prediabetes conditions and microalbuminuria. Nephro-urology monthly, 5(2), 741.
  • Black MJ, Lim K, Zimanyi MA, Sampson AK, Bubb KJ, Flower RL, Denton KM. (2015). Accelerated age-related decline in renal and vascular function in female rats following earlylife growth restriction. American Journal of PhysiologyRegulatory, Integrative and Comparative Physiology, 309(9), 1153-1161.
  • Böger CA, Gorski M, Li M, Hoffmann M.M, Huang C, Yang Q, Wichmann H.E. (2011). Association of eGFR-related loci identified by GWAS with incident CKD and ESRD. PLoS genetics, 7(9), e1002292.
  • Broek M, Leermakers ET, Jaddoe VW, Steegers EA, Rivadeneira F, Raat H, Kiefte-de Jong JC. (2015). Maternal dietary patterns during pregnancy and body composition of the child at age 6 y: the Generation R Study, 2. The American Journal of Clinical Nutrition, 102(4), 873-880.
  • Chu AY, Tin A, Schlosser P, Ko YA, Qiu C, Yao C, Liu C. (2017). Epigenome-wide association studies identify DNA methylation associated with kidney function. Nature Communications, 8(1), 1286.
  • Drougia A, Giapros V, Hotoura E, Papadopoulou F, Argyropoulou M, Andronikou S. (2008). The effects of gestational age and growth restriction on compensatory kidney growth. Nephrology Dialysis Transplantation, 24(1), 142-148.
  • Flegal KM, Carroll MD, Ogden CL, Curtin LR. (2010). Prevalence and trends in obesity among US adults, 1999-2008. Jama, 303(3), 235-241.
  • Gallo LA, Walton SL, Mazzuca MQ, Tare M, Parkington HC, Wlodek ME, Moritz KM. (2018). Uteroplacental insufficiency temporally exacerbates salt-induced hypertension associated with a reduced natriuretic response in male rat offspring. The Journal of Physiology, 587(11), 2635-2646.
  • Grigore D, Ojeda NB, Robertson EB, Dawson A S, Huffman CA, Bourassa EA, Alexander BT. (2007). Placental insufficiency results in temporal alterations in the renin angiotensin system in male hypertensive growth restricted offspring. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology, 293(2), R804-R811.
  • Hildebrandt F. (2010). Genetic kidney diseases. The Lancet, 375(9722), 1287-1295. Hill NR, Fatoba ST, Oke JL, Hirst JA, O’Callaghan CA, Lasserson DS, Hobbs FR. (2016). Global prevalence of chronic kidney disease–a systematic review and meta-analysis. PloS one, 11(7), e0158765.
  • Hokke SN, Armitage JA, Puelles VG. (2014). Altered ureteric branch-ing morphogenesis and nephron endowment in offspring of diabeticand insulin-treated pregnancy. Plos one, (8): 58243.
  • Ihnat MA, Thorpe JE, Ceriello A. (2007). Hypothesis: the ‘metabolic memory’, the new challenge of diabetes. Diabetic Medicine, 24(6), 582-586.
  • Jackson CM, Alexander BT, Roach L, Haggerty D, Marbury DC, Hutchens ZM, Maric-Bilkan C. (2011). Exposure to maternal overnutrition and a high-fat diet during early postnatal development increases susceptibility to renal and metabolic injury later in life. American Journal of Physiology-Renal Physiology, 302(6), F774-F783.
  • Kato M, Natarajan R. (2014). Diabetic nephropathy—emerging epigenetic mechanisms. Nature Reviews Nephrology, 10(9), 517.
  • Koleganova N, Piecha G, Ritz E, Becker LE, Müller A, Weckbach M, Gross-Weissmann M L. (2011). Both high and low maternal salt intake in pregnancy alter kidney development in the offspring. American Journal of Physiology-Renal Physiology, 301(2), F344-F354
  • Ligthart S. (2016). DNA methylation signatures of chronic lowgrade inflammation are associated with complex diseases. Genome Biol. 17, 255.
  • Macumber I, Schwartz S, Leca N. (2017). Maternal obesity is associated with congenital anomalies of the kidney and urinary tract in offspring. Pediatric Nephrology, 32(4), 635- 642.
  • Mata-Greenwood E, Sands L, Xiao D, Zhang L, Arlin B. (2017, March). Role of Renin-Angiotensin System Activation in a Rat Model of Placental Insufficiency and PregnancyInduced Hypertension. In reproductıve scıences. 24: 153A-153A.
  • Moritz KM, Mazzuca MQ, Siebel AL, Mibus A, Arena D, Tare M, Wlodek ME. (2009). Uteroplacental insufficiency causes a nephron deficit, modest renal insufficiency but no hypertension with ageing in female rats. The Journal of physiology, 587(11), 2635-2646.
  • Prior LJ, Davern PJ, Burke SL, Lim K, Armitage, JA, Head GA. (2014). Exposure to a High-Fat Diet During Development Alters Leptin and Ghrelin Sensitivity and Elevates Renal Sympathetic Nerve Activity and Arterial Pressure in Rabbit sNovelty and Significance. Hypertension, 63(2), 338-345.
  • Redon J, Pichler G, Martinez F. (2015). Glomerular Filtration Rate in Renal Damage. In Assessment of Preclinical Organ Damage in Hypertension , 165-170.
  • Richter VFI, Briffa JF, Moritz KM, Wlodek ME, Hryciw D.H. (2016). The role of maternal nutrition, metabolic function and the placenta in developmental programming of renal dysfunction. Clinical and Experimental Pharmacology and Physiology, 43(1), 135-141.
  • Rietveld CA, Medland SE, Derringer J, Yang J, Esko T, Martin NW, Albrecht E. (2013). GWAS of 126,559 individuals identifies genetic variants associated with educational attainment. Science, 340(6139), 1467-1471.
  • Tafti SA, Nast CC, Desai M, Amaya KE., Ross, MG, Magee TR. (2011). Maternal undernutrition upregulates apoptosis in offspring nephrogenesis. Journal of developmental origins of health and disease, 2(4), 226-235.
  • Thomas C, Thomas L. (2009). Renal failure–measuring the glomerular filtra-tion rate. Dtsch. Arztebl. Int, 106: 849–54. Vander Jagt, TA, Neugebauer MH, Morgan M, Bowden DW, Shah VO. (2015). Epigenetic profiles of pre-diabetes transitioning to type 2 diabetes and nephropathy. World Journal of Diabetes, 6(9), 1113.
  • Wagener FA, Dekker D, Berden JH, Scharstuhl A, Van der Vlag J. (2009). The role of reactive oxygen species in apoptosis of the diabetic kidney. Apoptosis, 14(12), 1451-1458.
  • Wlodek ME, Westcott K, Siebel AL, Owens JA, Moritz KM.Growth restriction before or after birth reduces nephron number andincreases blood pressure in male rats. Kidney Int. (74): 187–95
  • Wu L, Shi A, Zhu D, Bo L, Zhong Y, Wang J, Mao C. (2016). High sucrose intake during gestation increases angiotensin II type 1 receptor-mediated vascular contractility associated with epigenetic alterations in aged offspring rats. Peptides, 86133-144.
  • Yan J, Li X, Su R, Zhang K, Yang H. (2014). Long-term effects of maternaldiabetes on blood pressure and renal function in rat male offspring .Plos one, 9: e88269.59.

Epigenetics and Kidney Diseases

Yıl 2020, Cilt: 3 Sayı: 3, 161 - 166, 30.09.2020

Öz

Epigenetics is defined as hereditary changes that occur in the expression of a gene without a change in the DNA sequence. Studies in this area are often concerned with fetal origins of diseases and investigate the effects of uteroplecental exposures, which are mediators of environmental factors, on disease. In recent years, the number of epigenetics studies related to kidney diseases has been increasing and it has been reported that the nutritional profile affects epigenetic variations related to kidney diseases. These studies focus on the effects of fetal kidney function on maternal insufficiency or over nutrition, obesity and gestational diabetes. Accordingly, the nutritional habits of the mother directly or indirectly changes the nephron number, glomerulofiltration rate (GFR) and renin-angiotensin system (RAS) of the offspring and affects both in the post-natal period and later in life. In this review, we aimed to investigate the effect of maternal nutrition on the epigenetic parameters associated with renal function and nephropatic complications of the offspring.

Proje Numarası

yoktur.

Kaynakça

  • Alias NA, Aziz W, Amn WS, Mohamad C, Anuar C, Roslan R, Mohd Noor N. (2015). Effects of high and low maternal dietary sodium intake during pregnancy on the offsprings’ glomerular number in rats. 587 (11), 2635-2646.
  • Altunkaynak ME, Özbek E, Altunkaynak BZ, Can İ, Unal D, Unal B. (2008). The effects of high-fat diet on the renal structure and morphometric parametric of kidneys in rats. Journal of anatomy, 212(6), 845-852.
  • Armitage JA, Burke SL, Prior LJ, Barzel B, Eikelis N, Lim K, Head GA. (2012). Rapid onset of renal sympathetic nerve activation in rabbits fed a high-fat diet. Hypertension, 60,163–171.
  • Bahar A, Makhlough A, Yousefi A, Kashi Z, Abediankenari S. (2013). Correlation between prediabetes conditions and microalbuminuria. Nephro-urology monthly, 5(2), 741.
  • Black MJ, Lim K, Zimanyi MA, Sampson AK, Bubb KJ, Flower RL, Denton KM. (2015). Accelerated age-related decline in renal and vascular function in female rats following earlylife growth restriction. American Journal of PhysiologyRegulatory, Integrative and Comparative Physiology, 309(9), 1153-1161.
  • Böger CA, Gorski M, Li M, Hoffmann M.M, Huang C, Yang Q, Wichmann H.E. (2011). Association of eGFR-related loci identified by GWAS with incident CKD and ESRD. PLoS genetics, 7(9), e1002292.
  • Broek M, Leermakers ET, Jaddoe VW, Steegers EA, Rivadeneira F, Raat H, Kiefte-de Jong JC. (2015). Maternal dietary patterns during pregnancy and body composition of the child at age 6 y: the Generation R Study, 2. The American Journal of Clinical Nutrition, 102(4), 873-880.
  • Chu AY, Tin A, Schlosser P, Ko YA, Qiu C, Yao C, Liu C. (2017). Epigenome-wide association studies identify DNA methylation associated with kidney function. Nature Communications, 8(1), 1286.
  • Drougia A, Giapros V, Hotoura E, Papadopoulou F, Argyropoulou M, Andronikou S. (2008). The effects of gestational age and growth restriction on compensatory kidney growth. Nephrology Dialysis Transplantation, 24(1), 142-148.
  • Flegal KM, Carroll MD, Ogden CL, Curtin LR. (2010). Prevalence and trends in obesity among US adults, 1999-2008. Jama, 303(3), 235-241.
  • Gallo LA, Walton SL, Mazzuca MQ, Tare M, Parkington HC, Wlodek ME, Moritz KM. (2018). Uteroplacental insufficiency temporally exacerbates salt-induced hypertension associated with a reduced natriuretic response in male rat offspring. The Journal of Physiology, 587(11), 2635-2646.
  • Grigore D, Ojeda NB, Robertson EB, Dawson A S, Huffman CA, Bourassa EA, Alexander BT. (2007). Placental insufficiency results in temporal alterations in the renin angiotensin system in male hypertensive growth restricted offspring. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology, 293(2), R804-R811.
  • Hildebrandt F. (2010). Genetic kidney diseases. The Lancet, 375(9722), 1287-1295. Hill NR, Fatoba ST, Oke JL, Hirst JA, O’Callaghan CA, Lasserson DS, Hobbs FR. (2016). Global prevalence of chronic kidney disease–a systematic review and meta-analysis. PloS one, 11(7), e0158765.
  • Hokke SN, Armitage JA, Puelles VG. (2014). Altered ureteric branch-ing morphogenesis and nephron endowment in offspring of diabeticand insulin-treated pregnancy. Plos one, (8): 58243.
  • Ihnat MA, Thorpe JE, Ceriello A. (2007). Hypothesis: the ‘metabolic memory’, the new challenge of diabetes. Diabetic Medicine, 24(6), 582-586.
  • Jackson CM, Alexander BT, Roach L, Haggerty D, Marbury DC, Hutchens ZM, Maric-Bilkan C. (2011). Exposure to maternal overnutrition and a high-fat diet during early postnatal development increases susceptibility to renal and metabolic injury later in life. American Journal of Physiology-Renal Physiology, 302(6), F774-F783.
  • Kato M, Natarajan R. (2014). Diabetic nephropathy—emerging epigenetic mechanisms. Nature Reviews Nephrology, 10(9), 517.
  • Koleganova N, Piecha G, Ritz E, Becker LE, Müller A, Weckbach M, Gross-Weissmann M L. (2011). Both high and low maternal salt intake in pregnancy alter kidney development in the offspring. American Journal of Physiology-Renal Physiology, 301(2), F344-F354
  • Ligthart S. (2016). DNA methylation signatures of chronic lowgrade inflammation are associated with complex diseases. Genome Biol. 17, 255.
  • Macumber I, Schwartz S, Leca N. (2017). Maternal obesity is associated with congenital anomalies of the kidney and urinary tract in offspring. Pediatric Nephrology, 32(4), 635- 642.
  • Mata-Greenwood E, Sands L, Xiao D, Zhang L, Arlin B. (2017, March). Role of Renin-Angiotensin System Activation in a Rat Model of Placental Insufficiency and PregnancyInduced Hypertension. In reproductıve scıences. 24: 153A-153A.
  • Moritz KM, Mazzuca MQ, Siebel AL, Mibus A, Arena D, Tare M, Wlodek ME. (2009). Uteroplacental insufficiency causes a nephron deficit, modest renal insufficiency but no hypertension with ageing in female rats. The Journal of physiology, 587(11), 2635-2646.
  • Prior LJ, Davern PJ, Burke SL, Lim K, Armitage, JA, Head GA. (2014). Exposure to a High-Fat Diet During Development Alters Leptin and Ghrelin Sensitivity and Elevates Renal Sympathetic Nerve Activity and Arterial Pressure in Rabbit sNovelty and Significance. Hypertension, 63(2), 338-345.
  • Redon J, Pichler G, Martinez F. (2015). Glomerular Filtration Rate in Renal Damage. In Assessment of Preclinical Organ Damage in Hypertension , 165-170.
  • Richter VFI, Briffa JF, Moritz KM, Wlodek ME, Hryciw D.H. (2016). The role of maternal nutrition, metabolic function and the placenta in developmental programming of renal dysfunction. Clinical and Experimental Pharmacology and Physiology, 43(1), 135-141.
  • Rietveld CA, Medland SE, Derringer J, Yang J, Esko T, Martin NW, Albrecht E. (2013). GWAS of 126,559 individuals identifies genetic variants associated with educational attainment. Science, 340(6139), 1467-1471.
  • Tafti SA, Nast CC, Desai M, Amaya KE., Ross, MG, Magee TR. (2011). Maternal undernutrition upregulates apoptosis in offspring nephrogenesis. Journal of developmental origins of health and disease, 2(4), 226-235.
  • Thomas C, Thomas L. (2009). Renal failure–measuring the glomerular filtra-tion rate. Dtsch. Arztebl. Int, 106: 849–54. Vander Jagt, TA, Neugebauer MH, Morgan M, Bowden DW, Shah VO. (2015). Epigenetic profiles of pre-diabetes transitioning to type 2 diabetes and nephropathy. World Journal of Diabetes, 6(9), 1113.
  • Wagener FA, Dekker D, Berden JH, Scharstuhl A, Van der Vlag J. (2009). The role of reactive oxygen species in apoptosis of the diabetic kidney. Apoptosis, 14(12), 1451-1458.
  • Wlodek ME, Westcott K, Siebel AL, Owens JA, Moritz KM.Growth restriction before or after birth reduces nephron number andincreases blood pressure in male rats. Kidney Int. (74): 187–95
  • Wu L, Shi A, Zhu D, Bo L, Zhong Y, Wang J, Mao C. (2016). High sucrose intake during gestation increases angiotensin II type 1 receptor-mediated vascular contractility associated with epigenetic alterations in aged offspring rats. Peptides, 86133-144.
  • Yan J, Li X, Su R, Zhang K, Yang H. (2014). Long-term effects of maternaldiabetes on blood pressure and renal function in rat male offspring .Plos one, 9: e88269.59.
Toplam 32 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Konular Sağlık Kurumları Yönetimi
Bölüm Araştırma Makaleleri
Yazarlar

Ümüş Özbey Yücel

Aslı Akyol Mutlu 0000-0001-6301-6358

Proje Numarası yoktur.
Yayımlanma Tarihi 30 Eylül 2020
Gönderilme Tarihi 28 Nisan 2020
Yayımlandığı Sayı Yıl 2020 Cilt: 3 Sayı: 3

Kaynak Göster

APA Özbey Yücel, Ü., & Akyol Mutlu, A. (2020). Epigenetik ve Böbrek Hastalıkları. Avrasya Sağlık Bilimleri Dergisi, 3(3), 161-166.
AMA Özbey Yücel Ü, Akyol Mutlu A. Epigenetik ve Böbrek Hastalıkları. AvrasyaSBD. Eylül 2020;3(3):161-166.
Chicago Özbey Yücel, Ümüş, ve Aslı Akyol Mutlu. “Epigenetik Ve Böbrek Hastalıkları”. Avrasya Sağlık Bilimleri Dergisi 3, sy. 3 (Eylül 2020): 161-66.
EndNote Özbey Yücel Ü, Akyol Mutlu A (01 Eylül 2020) Epigenetik ve Böbrek Hastalıkları. Avrasya Sağlık Bilimleri Dergisi 3 3 161–166.
IEEE Ü. Özbey Yücel ve A. Akyol Mutlu, “Epigenetik ve Böbrek Hastalıkları”, AvrasyaSBD, c. 3, sy. 3, ss. 161–166, 2020.
ISNAD Özbey Yücel, Ümüş - Akyol Mutlu, Aslı. “Epigenetik Ve Böbrek Hastalıkları”. Avrasya Sağlık Bilimleri Dergisi 3/3 (Eylül 2020), 161-166.
JAMA Özbey Yücel Ü, Akyol Mutlu A. Epigenetik ve Böbrek Hastalıkları. AvrasyaSBD. 2020;3:161–166.
MLA Özbey Yücel, Ümüş ve Aslı Akyol Mutlu. “Epigenetik Ve Böbrek Hastalıkları”. Avrasya Sağlık Bilimleri Dergisi, c. 3, sy. 3, 2020, ss. 161-6.
Vancouver Özbey Yücel Ü, Akyol Mutlu A. Epigenetik ve Böbrek Hastalıkları. AvrasyaSBD. 2020;3(3):161-6.