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Effect of early postnatal nutrition on chronic kidney disease and arterial hypertension in adulthood: a narrative review

Part of: French DOHaD

Published online by Cambridge University Press:  06 August 2018

C. Juvet ,
U. Simeoni ,
C. Yzydorczyk ,
B. Siddeek ,
J.-B. Armengaud ,
K. Nardou ,
P. Juvet ,
M. Benahmed ,
F. Cachat  and
H. Chehade
C. Juvet*
Affiliation:
Division of Pediatrics, DOHaD Laboratory, woman-mother-child department, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland Division of Pediatrics, pediatric nephrology unit, woman-mother-child department, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland
U. Simeoni
Affiliation:
Division of Pediatrics, DOHaD Laboratory, woman-mother-child department, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland Division of Pediatrics, pediatric nephrology unit, woman-mother-child department, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland Division of Pediatrics, woman-mother-child department, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland
C. Yzydorczyk
Affiliation:
Division of Pediatrics, DOHaD Laboratory, woman-mother-child department, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland
B. Siddeek
Affiliation:
Division of Pediatrics, DOHaD Laboratory, woman-mother-child department, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland
J.-B. Armengaud
Affiliation:
Division of Pediatrics, DOHaD Laboratory, woman-mother-child department, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland Division of Pediatrics, pediatric nephrology unit, woman-mother-child department, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland Division of Pediatrics, woman-mother-child department, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland
K. Nardou
Affiliation:
Division of Pediatrics, DOHaD Laboratory, woman-mother-child department, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland Division of Pediatrics, pediatric nephrology unit, woman-mother-child department, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland
P. Juvet
Affiliation:
Division of Pediatrics, woman-mother-child department, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland
M. Benahmed
Affiliation:
Division of Pediatrics, DOHaD Laboratory, woman-mother-child department, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland
F. Cachat
Affiliation:
Division of Pediatrics, pediatric nephrology unit, woman-mother-child department, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland
H. Chehade
Affiliation:
Division of Pediatrics, DOHaD Laboratory, woman-mother-child department, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland Division of Pediatrics, pediatric nephrology unit, woman-mother-child department, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland
*
Address for correspondence: C. Juvet, DOHaD Laboratory, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Rue du Bugnon 27, 1005 Lausanne, Switzerland. E-mail: [email protected]
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Abstract

Intrauterine growth restriction (IUGR) has been identified as a risk factor for adult chronic kidney disease (CKD), including hypertension (HTN). Accelerated postnatal catch-up growth superimposed to IUGR has been shown to further increase the risk of CKD and HTN. Although the impact of excessive postnatal growth without previous IUGR is less clear, excessive postnatal overfeeding in experimental animals shows a strong impact on the risk of CKD and HTN in adulthood. On the other hand, food restriction in the postnatal period seems to have a protective effect on CKD programming. All these effects are mediated at least partially by the activation of the renin–angiotensin system, leptin and neuropeptide Y (NPY) signaling and profibrotic pathways. Early nutrition, especially in the postnatal period has a significant impact on the risk of CKD and HTN at adulthood and should receive specific attention in the prevention of CKD and HTN.

Keywords

chronic kidney diseaseDevelopmental Origins of Health and Diseasehypertensionprogramming
Type
Review
Information
Journal of Developmental Origins of Health and Disease , Volume 9 , Issue 6 , December 2018 , pp. 598 - 614
Copyright
© Cambridge University Press and the International Society for Developmental Origins of Health and Disease 2018 

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Footnotes

†

These authors contributed equally to this work.

References

1. Barker, DJ, Winter, PD, Osmond, C, Margetts, B, Simmonds, SJ. Weight in infancy and death from ischaemic heart disease. Lancet. 1989; 2, 577–580.Google Scholar
2. Roseboom, TJ, van der Meulen, JH, Ravelli, AC, et al. Effects of prenatal exposure to the Dutch famine on adult disease in later life: an overview. Twin Res. 2001; 4, 293–298.Google Scholar
3. Lackland, DT, Bendall, HE, Osmond, C, Egan, BM, Barker, DJ. Low birth weights contribute to high rates of early-onset chronic renal failure in the Southeastern United States. Arch Intern Med. 2000; 160, 1472–1476.Google Scholar
4. Keijzer-Veen, MG, Schrevel, M, Finken, MJ, et al. Microalbuminuria and lower glomerular filtration rate at young adult age in subjects born very premature and after intrauterine growth retardation. J Am Soc Nephrol. 2005; 16, 2762–2768.Google Scholar
5. Dotsch, J, Plank, C, Amann, K. Fetal programming of renal function. Pediatr Nephrol. 2012; 27, 513–520.Google Scholar
6. Boubred, F, Saint-Faust, M, Buffat, C, et al. Developmental origins of chronic renal disease: an integrative hypothesis. Int J Nephrol. 2013; 2013, 346067.Google Scholar
7. Luyckx, VA, Brenner, BM. Birth weight, malnutrition and kidney-associated outcomes – a global concern. Nat Rev Nephrol. 2015; 11, 135–149.Google Scholar
8. Luyckx, VA, Brenner, BM. Low birth weight, nephron number, and kidney disease. Kidney Int Suppl. 2005; 68, S68–S77.Google Scholar
9. Brenner, BM, Garcia, DL, Anderson, S. Glomeruli and blood pressure. Less of one, more the other? Am J Hypertens. 1988; 1(Pt 1), 335–347.Google Scholar
10. Bagby, SP. Maternal nutrition, low nephron number, and hypertension in later life: pathways of nutritional programming. J Nutr. 2007; 137, 1066–1072.Google Scholar
11. Simonetti, GD, Raio, L, Surbek, D, et al. Salt sensitivity of children with low birth weight. Hypertension. 2008; 52, 625–630.Google Scholar
12. de Boer, MP, Ijzerman, RG, de Jongh, RT, et al. Birth weight relates to salt sensitivity of blood pressure in healthy adults. Hypertension. 2008; 51, 928–932.Google Scholar
13. Alwasel, SH, Ashton, N. Prenatal programming of renal sodium handling in the rat. Clin Sci (Lond). 2009; 117, 75–84.Google Scholar
14. Ojeda, NB, Johnson, WR, Dwyer, TM, Alexander, BT. Early renal denervation prevents development of hypertension in growth-restricted offspring. Clin Exp Pharmacol Physiol. 2007; 34, 1212–1216.Google Scholar
15. Luyckx VA, Perico N, Somaschini M, et al. A developmental approach to the prevention of hypertension and kidney disease: a report from the Low Birth Weight and Nephron Number Working Group. Lancet. 2017; 390, 424–428.Google Scholar
16. Moritz, KM, Singh, RR, Probyn, ME, Denton, KM. Developmental programming of a reduced nephron endowment: more than just a baby’s birth weight. Am J Physiol Renal Physiol. 2009; 296, F1–F9.Google Scholar
17. Simeoni, U, Barker, DJ. Offspring of diabetic pregnancy: long-term outcomes. Semin Fetal Neonatal Med. 2009; 14, 119–124.Google Scholar
18. Lelievre-Pegorier, M, Vilar, J, Ferrier, ML, et al. Mild vitamin A deficiency leads to inborn nephron deficit in the rat. Kidney Int. 1998; 54, 1455–1462.Google Scholar
19. Hoy, WE, Bertram, JF, Denton, RD, et al. Nephron number, glomerular volume, renal disease and hypertension. Curr Opin Nephrol Hypertens. 2008; 17, 258–265.Google Scholar
20. Hoy, WE, Ingelfinger, JR, Hallan, S, et al. The early development of the kidney and implications for future health. J Dev Orig Health Dis. 2010; 1, 216–233.Google Scholar
21. Hoy, WE, Kincaid-Smith, P, Hughson, MD, et al. CKD in Aboriginal Australians. Am J Kidney Dis. 2010; 56, 983–993.Google Scholar
22. Lucas, A, Morley, R, Cole, TJ. Randomised trial of early diet in preterm babies and later intelligence quotient. BMJ. 1998; 317, 1481–1487.Google Scholar
23. Pylipow, M, Spector, LG, Puumala, SE, et al. Early postnatal weight gain, intellectual performance, and body mass index at 7 years of age in term infants with intrauterine growth restriction. J Pediatr. 2009; 154, 201–206.Google Scholar
24. Barker, DJ, Forsen, T, Eriksson, JG, Osmond, C. Growth and living conditions in childhood and hypertension in adult life: a longitudinal study. J Hypertens. 2002; 20, 1951–1956.Google Scholar
25. Taine, M, Stengel, B, Forhan, A, et al. Rapid early growth may modulate the association between birth weight and blood pressure at 5 years in the EDEN cohort study. Hypertension. 2016; 68, 859–865.Google Scholar
26. Zhao, M, Shu, XO, Jin, F, et al. Birthweight, childhood growth and hypertension in adulthood. Int J Epidemiol. 2002; 31, 1043–1051.Google Scholar
27. Adair, LS, Cole, TJ. Rapid child growth raises blood pressure in adolescent boys who were thin at birth. Hypertension. 2003; 41, 451–456.Google Scholar
28. Singhal, A, Cole, TJ, Fewtrell, M, et al. Promotion of faster weight gain in infants born small for gestational age: is there an adverse effect on later blood pressure? Circulation. 2007; 115, 213–220.Google Scholar
29. Eriksson, JG, Forsen, TJ, Kajantie, E, Osmond, C, Barker, DJ. Childhood growth and hypertension in later life. Hypertension. 2007; 49, 1415–1421.Google Scholar
30. Eriksson, J, Forsen, T, Tuomilehto, J, Osmond, C, Barker, D. Fetal and childhood growth and hypertension in adult life. Hypertension. 2000; 36, 790–794.Google Scholar
31. Huang, RC, Burrows, S, Mori, TA, Oddy, WH, Beilin, LJ. Lifecourse adiposity and blood pressure between birth and 17 years old. Am J Hypertens. 2015; 28, 1056–1063.Google Scholar
32. Tauzin, L, Rossi, P, Grosse, C, et al. Increased systemic blood pressure and arterial stiffness in young adults born prematurely. J Dev Orig Health Dis. 2014; 5, 448–452.Google Scholar
33. Cruickshank, JK, Mzayek, F, Liu, L, et al. Origins of the “black/white” difference in blood pressure: roles of birth weight, postnatal growth, early blood pressure, and adolescent body size: the Bogalusa heart study. Circulation. 2005; 111, 1932–1937.Google Scholar
34. Cheung, YB, Low, L, Osmond, C, Barker, D, Karlberg, J. Fetal growth and early postnatal growth are related to blood pressure in adults. Hypertension. 2000; 36, 795–800.Google Scholar
35. Sterling, R, Checkley, W, Gilman, RH, et al. Beyond birth-weight: early growth and adolescent blood pressure in a Peruvian population. PeerJ. 2014; 2, e381.Google Scholar
36. Hardy, R, Wadsworth, ME, Langenberg, C, Kuh, D. Birthweight, childhood growth, and blood pressure at 43 years in a British birth cohort. Int J Epidemiol. 2004; 33, 121–129.Google Scholar
37. Adair, LS, Martorell, R, Stein, AD, et al. Size at birth, weight gain in infancy and childhood, and adult blood pressure in 5 low- and middle-income-country cohorts: when does weight gain matter? Am J Clin Nutr. 2009; 89, 1383–1392.Google Scholar
38. Adair, LS, Fall, CH, Osmond, C, et al. Associations of linear growth and relative weight gain during early life with adult health and human capital in countries of low and middle income: findings from five birth cohort studies. Lancet. 2013; 382, 525–534.Google Scholar
39. Kagura, J, Adair, LS, Munthali, RJ, Pettifor, JM, Norris, SA. Association between early life growth and blood pressure trajectories in Black South African children. Hypertension . 2016; 68, 1123–1131.Google Scholar
40. Law, CM. Fetal, infant, and childhood growth and adult blood pressure: a longitudinal study from birth to 22 years of age. Circulation. 2002; 105, 1088–1092.Google Scholar
41. Bansal, N, Ayoola, OO, Gemmell, I, et al. Effects of early growth on blood pressure of infants of British European and South Asian origin at one year of age: the Manchester children’s growth and vascular health study. J Hypertens. 2008; 26, 412–418.Google Scholar
42. Hemachandra, AH, Howards, PP, Furth, SL, Klebanoff, MA. Birth weight, postnatal growth, and risk for high blood pressure at 7 years of age: results from the Collaborative Perinatal Project. Pediatrics. 2007; 119, e1264–e1270.Google Scholar
43. Horta, BL, Barros, FC, Victora, CG, Cole, TJ. Early and late growth and blood pressure in adolescence. J Epidemiol Community Health. 2003; 57, 226–230.Google Scholar
44. Järvelin, MR, Sovio, U, King, V, et al. Early life factors and blood pressure at age 31 years in the 1966 northern Finland birth cohort. Hypertension. 2004; 44, 838–846.Google Scholar
45. Ben-Shlomo, Y, McCarthy, A, Hughes, R, et al. Immediate postnatal growth is associated with blood pressure in young adulthood: the Barry Caerphilly Growth Study. Hypertension. 2008; 52, 638–644.Google Scholar
46. Boyne, MS, Osmond, C, Fraser, RA, et al. Developmental origins of cardiovascular risk in Jamaican children: the Vulnerable Windows Cohort study. Br J Nutr. 2010; 104, 1026–1033.Google Scholar
47. Nowson, CA, Crozier, SR, Robinson, SM, et al. Association of early childhood abdominal circumference and weight gain with blood pressure at 36 months of age: secondary analysis of data from a prospective cohort study. BMJ Open. 2014; 4, e005412.Google Scholar
48. Antonisamy, B, Vasan, SK, Geethanjali, FS, et al. Weight gain and height growth during infancy, childhood, and adolescence as predictors of adult cardiovascular risk. J Pediatr. 2017; 180, 53–61.e53.Google Scholar
49. Jones, A, Charakida, M, Falaschetti, E, et al. Adipose and height growth through childhood and blood pressure status in a large prospective cohort study. Hypertension. 2012; 59, 919–925.Google Scholar
50. Holland, FJ, Stark, O, Ades, AE, Peckham, CS. Birth weight and body mass index in childhood, adolescence, and adulthood as predictors of blood pressure at age 36. J Epidemiol Community Health. 1993; 47, 432–435.Google Scholar
51. Schack-Nielsen, L, Holst, C, Sorensen, TI. Blood pressure in relation to relative weight at birth through childhood and youth in obese and non-obese adult men. Int J Obes Relat Metab Disord. 2002; 26, 1539–1546.Google Scholar
52. Perng, W, Rifas-Shiman, SL, Kramer, MS, et al. Early weight gain, linear growth, and mid-childhood blood pressure: a prospective study in project viva. Hypertension. 2016; 67, 301–308.Google Scholar
53. de Beer, M, Vrijkotte, TG, Fall, CH, et al. Associations of infant feeding and timing of weight gain and linear growth during early life with childhood blood pressure: findings from a prospective population based cohort study. PLoS One. 2016; 11, e0166281.Google Scholar
54. Cournil, A, Coly, AN, Diallo, A, Simondon, KB. Enhanced post-natal growth is associated with elevated blood pressure in young Senegalese adults. Int J Epidemiol. 2009; 38, 1401–1410.Google Scholar
55. Chiolero, A, Paradis, G, Bovet, P. Which period of growth is determinant for blood pressure? Hypertension. 2012; 60, e10; author reply e11.Google Scholar
56. Chiolero, A, Kaufman, JS, Paradis, G. Why adjustment for current weight can bias the estimate of the effect of birth weight on blood pressure: shedding light using causal graphs. J Hypertens. 2012; 30, 1042–1045.Google Scholar
57. Stein, AD, Zybert, PA, van der Pal-de Bruin, K, Lumey, LH. Exposure to famine during gestation, size at birth, and blood pressure at age 59 y: evidence from the Dutch Famine. Eur J Epidemiol. 2006; 21, 759–765.Google Scholar
58. Xin, X, Yao, J, Yang, F, Zhang, D. Famine exposure during early life and risk of hypertension in adulthood: A meta-analysis. Crit Rev Food Sci Nutr. 2017; 1–8 doi:10.1080/10408398.2017.1322551.Google Scholar
59. Martin, RM, Gunnell, D, Smith, GD. Breastfeeding in infancy and blood pressure in later life: systematic review and meta-analysis. Am J Epidemiol. 2005; 161, 15–26.Google Scholar
60. Fergusson, DM, McLeod, GF, Horwood, LJ. Breast feeding, infant growth, and body mass index at 30 and 35 years. Paediatr Perinat Epidemiol. 2014; 28, 545–552.Google Scholar
61. Geleijnse, JM, Hofman, A, Witteman, JCM, et al. Long-term Effects of neonatal sodium restriction on blood pressure. Hypertension. 1997; 29, 913–917.Google Scholar
62. Maslin, K, Grimshaw, K, Oliver, E, et al. Taste preference, food neophobia and nutritional intake in children consuming a cows’ milk exclusion diet: a prospective study. J Hum Nutr Diet. 2016; 29, 786–796.Google Scholar
63. Smriga, M, Kameishi, M, Torii, K. Brief exposure to NaCl during early postnatal development enhances adult intake of sweet and salty compounds. Neuroreport. 2002; 13, 2565–2569.Google Scholar
64. Brenna, JT, Varamini, B, Jensen, RG, et al. Docosahexaenoic and arachidonic acid concentrations in human breast milk worldwide. Am J Clin Nutr. 2007; 85, 1457–1464.Google Scholar
65. Forsyth, JS, Willatts, P, Agostoni, C, et al. Long chain polyunsaturated fatty acid supplementation in infant formula and blood pressure in later childhood: follow up of a randomised controlled trial. BMJ. 2003; 326, 953.Google Scholar
66. Decsi, T, Thiel, I, Koletzko, B. Essential fatty acids in full term infants fed breast milk or formula. Arch Dis Child Fetal Neonatal Ed. 1995; 72, F23–F28.Google Scholar
67. van Gijssel, RM, Braun, KV, Kiefte-de Jong, JC, et al. Associations between dietary fiber intake in infancy and cardiometabolic health at school age: the Generation R study. Nutrients. 2016; 8, 281–294.Google Scholar
68. Voortman, T, van den Hooven, EH, Tielemans, MJ, et al. Protein intake in early childhood and cardiometabolic health at school age: the Generation R Study. Eur J Nutr. 2016; 55, 2117–2127.Google Scholar
69. Bakker, H, Gaillard, R, Franco, OH, et al. Fetal and infant growth patterns and kidney function at school age. J Am Soc Nephrol. 2014; 25, 2607–2615.Google Scholar
70. Bacchetta, J, Harambat, J, Dubourg, L, et al. Both extrauterine and intrauterine growth restriction impair renal function in children born very preterm. Kidney Int. 2009; 76, 445–452.Google Scholar
71. Escribano, J, Luque, V, Ferre, N, et al. Increased protein intake augments kidney volume and function in healthy infants. Kidney Int. 2011; 79, 783–790.Google Scholar
72. Bakker, H, Kooijman, MN, van der Heijden, AJ, et al. Kidney size and function in a multi-ethnic population-based cohort of school-age children. Pediatr Nephrol. 2014; 29, 1589–1598.Google Scholar
73. Adibi, A, Adibi, I, Khosravi, P. Do kidney sizes in ultrasonography correlate to glomerular filtration rate in healthy children? Australas Radiol. 2007; 51, 555–559.Google Scholar
74. Ojeda, NB, Grigore, D, Alexander, BT. Intrauterine growth restriction: fetal programming of hypertension and kidney disease. Adv Chronic Kidney Dis. 2008; 15, 101–106.Google Scholar
75. Shen, Q, Xu, H, Wei, LM, Chen, J, Liu, HM. Intrauterine growth restriction and postnatal high-protein diet affect the kidneys in adult rats. Nutrition. 2011; 27, 364–371.Google Scholar
76. Vickers, MH, Breier, BH, Cutfield, WS, Hofman, PL, Gluckman, PD. Fetal origins of hyperphagia, obesity, and hypertension and postnatal amplification by hypercaloric nutrition. Am J Physiol Endocrinol Metab. 2000; 279, E83–E87.Google Scholar
77. Boubred, F, Delamaire, E, Buffat, C, et al. High protein intake in neonatal period induces glomerular hypertrophy and sclerosis in adulthood in rats born with IUGR. Pediatr Res. 2016; 79, 22–26.Google Scholar
78. Boubred, F, Daniel, L, Buffat, C, et al. Early postnatal overfeeding induces early chronic renal dysfunction in adult male rats. Am J Physiol Renal Physiol. 2009; 297, F943–F951.Google Scholar
79. Boubred, F, Buffat, C, Feuerstein, JM, et al. Effects of early postnatal hypernutrition on nephron number and long-term renal function and structure in rats. Am J Physiol Renal Physiol. 2007; 293, F1944–F1949.Google Scholar
80. Yim, HE, Ha, KS, Bae, IS, et al. Overweight, hypertension and renal dysfunction in adulthood of neonatally overfed rats. J Nutr Biochem. 2013; 24, 1324–1333.Google Scholar
81. Yim, HE, Yoo, KH, Bae, IS, Hong, YS, Lee, JW. Postnatal early overnutrition causes long-term renal decline in aging male rats. Pediatr Res. 2014; 75, 259–265.Google Scholar
82. Alcazar, MA, Boehler, E, Rother, E, et al. Early postnatal hyperalimentation impairs renal function via SOCS-3 mediated renal postreceptor leptin resistance. Endocrinology. 2012; 153, 1397–1410.Google Scholar
83. Habbout, A, Li, N, Rochette, L, Vergely, C. Postnatal overfeeding in rodents by litter size reduction induces major short- and long-term pathophysiological consequences. J Nutr. 2013; 143, 553–562.Google Scholar
84. Alejandre Alcazar, MA, Boehler, E, Amann, K, et al. Persistent changes within the intrinsic kidney-associated NPY system and tubular function by litter size reduction. Nephrol Dial Transplant. 2011; 26, 2453–2465.Google Scholar
85. Hoppe, CC, Evans, RG, Moritz, KM, et al. Combined prenatal and postnatal protein restriction influences adult kidney structure, function, and arterial pressure. Am J Physiol Regul Integr Comp Physiol. 2007; 292, R462–R469.Google Scholar
86. Petry, CJ, Jennings, BJ, James, LA, Hales, CN, Ozanne, SE. Suckling a protein-restricted rat dam leads to diminished albuminuria in her male offspring in adult life: a longitudinal study. BMC Nephrol. 2006; 7, 14.Google Scholar
87. Tarry-Adkins, JL, Joles, JA, Chen, JH, et al. Protein restriction in lactation confers nephroprotective effects in the male rat and is associated with increased antioxidant expression. Am J Physiol Regul Integr Comp Physiol. 2007; 293, R1259–R1266.Google Scholar
88. Wlodek, ME, Westcott, K, Siebel, AL, Owens, JA, Moritz, KM. Growth restriction before or after birth reduces nephron number and increases blood pressure in male rats. Kidney Int. 2008; 74, 187–195.Google Scholar
89. Wlodek, ME, Mibus, A, Tan, A, et al. Normal lactational environment restores nephron endowment and prevents hypertension after placental restriction in the rat. J Am Soc Nephrol. 2007; 18, 1688–1696.Google Scholar
90. Peter, RF, Gugusheff, J, Wooldridge, AL, Gatford, KL, Muhlhausler, BS. Placental restriction in multi-fetal pregnancies and between-twin differences in size at birth alter neonatal feeding behaviour in the sheep. J Dev Orig Health Dis. 2017; 8, 357–369.Google Scholar
91. Padia, SH, Carey, RM. AT2 receptors: beneficial counter-regulatory role in cardiovascular and renal function. Pflugers Arch. 2013; 465, 99–110.Google Scholar
92. Yim, HE, Ha, KS, Bae, IS, et al. Postnatal early overnutrition dysregulates the intrarenal renin-angiotensin system and extracellular matrix-linked molecules in juvenile male rats. J Nutr Biochem. 2012; 23, 937–945.Google Scholar
93. Granado, M, Amor, S, Fernandez, N, et al. Effects of early overnutrition on the renal response to Ang II and expression of RAAS components in rat renal tissue. Nutr Metab Cardiovasc Dis. 2017; 27, 930–937.Google Scholar
94. Torretti, J. Sympathetic control of renin release. Annu Rev Pharmacol Toxicol. 1982; 22, 167–192.Google Scholar
95. Sherman, RC, Langley-Evans, SC. Early administration of angiotensin-converting enzyme inhibitor captopril, prevents the development of hypertension programmed by intrauterine exposure to a maternal low-protein diet in the rat. Clin Sci. 1998; 94, 373–381.Google Scholar
96. Sherman, RC, Langley-Evans, SC. Antihypertensive treatment in early postnatal life modulates prenatal dietary influences upon blood pressure in the rat. Clin Sci. 2000; 98, 269–275.Google Scholar
97. Yim, HE, Yoo, KH, Bae, IS, Hong, YS. Early treatment with enalapril and later renal injury in programmed obese adult rats. J Cell Physiol. 2017; 232, 447–455.Google Scholar
98. Simeoni, U, Ligi, I, Buffat, C, Boubred, F. Adverse consequences of accelerated neonatal growth: cardiovascular and renal issues. Pediatr Nephrol. 2011; 26, 493–508.Google Scholar
99. Dotsch, J, Plank, C, Amann, K, Ingelfinger, J. The implications of fetal programming of glomerular number and renal function. J Mol Med. 2009; 87, 841–848.Google Scholar
100. Woods, LL, Ingelfinger, JR, Nyengaard, JR, Rasch, R. Maternal protein restriction suppresses the newborn renin-angiotensin system and programs adult hypertension in rats. Pediatr Res. 2001; 49, 460–467.Google Scholar
101. Correia-Melo, C, Hewitt, G, Passos, JF. Telomeres, oxidative stress and inflammatory factors: partners in cellular senescence? Longev Healthspan. 2014; 3, 1.Google Scholar
102. Sturmlechner, I, Durik, M, Sieben, CJ, Baker, DJ, van Deursen, JM. Cellular senescence in renal ageing and disease. Nat Rev Nephrol. 2017; 13, 77–89.Google Scholar
103. Walsh, ME, Shi, Y, Van Remmen, H. The effects of dietary restriction on oxidative stress in rodents. Free Radic Biol Med. 2014; 66, 88–99.Google Scholar
104. Samocha-Bonet, D, Campbell, LV, Mori, TA, et al. Overfeeding reduces insulin sensitivity and increases oxidative stress, without altering markers of mitochondrial content and function in humans. PLoS One. 2012; 7, e36320.Google Scholar
105. Jennings, BJ, Ozanne, SE, Dorling, MW, Hales, CN. Early growth determines longevity in male rats and may be related to telomere shortening in the kidney. FEBS Lett. 1999; 448, 4–8.Google Scholar
106. Tarry-Adkins, JL, Ozanne, SE, Norden, A, Cherif, H, Hales, CN. Lower antioxidant capacity and elevated p53 and p21 may be a link between gender disparity in renal telomere shortening, albuminuria, and longevity. Am J Physiol Renal Physiol. 2006; 290, F509–F516.Google Scholar
107. Wolf, G, Chen, S, Han, DC, Ziyadeh, FN. Leptin and renal disease. Am J Kidney Dis. 2002; 39, 1–11.Google Scholar
108. Beltowski, J, Jamroz-Wisniewska, A, Borkowska, E, Wojcicka, G. Up-regulation of renal Na+, K+-ATPase: the possible novel mechanism of leptin-induced hypertension. Pol J Pharmacol. 2004; 56, 213–222.Google Scholar
109. Bischoff, A, Michel, MC. Renal effects of neuropeptide Y. Pflugers Arch. 1998; 435, 443–453.Google Scholar
110. Leite, RD, Kraemer-Aguiar, LG, Boa, BC, et al. Muscle endothelial-dependent microvascular dysfunction in adulthood due to early postnatal overnutrition. Microvasc Res. 2012; 84, 94–98.Google Scholar
111. Coatmellec-Taglioni, G, Dausse, JP, Giudicelli, Y, Ribiere, C. Sexual dimorphism in cafeteria diet-induced hypertension is associated with gender-related difference in renal leptin receptor down-regulation. J Pharmacol Exp Ther. 2003; 305, 362–367.Google Scholar
112. Emanuel, I, Filakti, H, Alberman, E, Evans, SJ. Intergenerational studies of human birthweight from the 1958 birth cohort. 1. Evidence for a multigenerational effect. Br J Obstet Gynaecol. 1992; 99, 67–74.Google Scholar
113. Unterberger, A, Szyf, M, Nathanielsz, PW, Cox, LA. Organ and gestational age effects of maternal nutrient restriction on global methylation in fetal baboons. J Med Primatol. 2009; 38, 219–227.Google Scholar
114. Mouillet, JF, Chu, T, Hubel, CA, et al. The levels of hypoxia-regulated microRNAs in plasma of pregnant women with fetal growth restriction. Placenta. 2010; 31, 781–784.Google Scholar
115. Huang, L, Shen, Z, Xu, Q, et al. Increased levels of microRNA-424 are associated with the pathogenesis of fetal growth restriction. Placenta. 2013; 34, 624–627.Google Scholar
116. Pham, TD, MacLennan, NK, Chiu, CT, et al. Uteroplacental insufficiency increases apoptosis and alters p53 gene methylation in the full-term IUGR rat kidney. Am J Physiol Regul Integr Comp Physiol. 2003; 285, R962–R970.Google Scholar
117. Bogdarina, I, Welham, S, King, PJ, Burns, SP, Clark, AJ. Epigenetic modification of the renin-angiotensin system in the fetal programming of hypertension. Circ Res. 2007; 100, 520–526.Google Scholar
118. Rodriguez, MM, Gomez, AH, Abitbol, CL, et al. Histomorphometric analysis of postnatal glomerulogenesis in extremely preterm infants. Pediatr Dev Pathol. 2004; 7, 17–25.Google Scholar
119. Martin, RM, McCarthy, A, Smith, GD, Davies, DP, Ben-Shlomo, Y. Infant nutrition and blood pressure in early adulthood: the Barry Caerphilly Growth study. Am J Clin Nutr. 2003; 77, 1489–1497.Google Scholar
120. Ekelund, U, Ong, KK, Linne, Y, et al. Association of weight gain in infancy and early childhood with metabolic risk in young adults. J Clin Endocrinol Metab. 2007; 92, 98–103.Google Scholar