Fetal programming of renal function

被引:21
|
作者
Doetsch, Joerg [1 ]
Plank, Christian [2 ]
Amann, Kerstin [3 ]
机构
[1] Univ Cologne, Dept Pediat, D-50937 Cologne, Germany
[2] Univ Erlangen Nurnberg, Dept Pediat, D-91054 Erlangen, Germany
[3] Univ Erlangen Nurnberg, Dept Nephropathol, D-91054 Erlangen, Germany
关键词
Fetal programming; Low birth weight; Glomerulonephritis; Chronic renal failure; Nephrotic syndrome; Diabetes mellitus; LOW-BIRTH-WEIGHT; INTRAUTERINE GROWTH-RETARDATION; MATERNAL PROTEIN RESTRICTION; CHANGE NEPHROTIC SYNDROME; RENIN-ANGIOTENSIN SYSTEM; FOR-GESTATIONAL-AGE; 11-BETA-HYDROXYSTEROID DEHYDROGENASE TYPE-2; SOUTHEASTERN UNITED-STATES; HENOCH-SCHONLEIN NEPHRITIS; ADULT-BLOOD PRESSURE;
D O I
10.1007/s00467-011-1781-5
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Results from large epidemiological studies suggest a clear relation between low birth weight and adverse renal outcome evident as early as during childhood. Such adverse outcomes may include glomerular disease, hypertension, and renal failure and contribute to a phenomenon called fetal programming. Other factors potentially leading to an adverse renal outcome following fetal programming are maternal diabetes mellitus, smoking, salt overload, and use of glucocorticoids during pregnancy. However, clinical data on the latter are scarce. Here, we discuss potential underlying mechanisms of fetal programming, including reduced nephron number via diminished nephrogenesis and other renal (e.g., via the intrarenal renin-angiotensin-aldosterone system) and non-renal (e.g., changes in endothelial function) alterations. It appears likely that the outcomes of fetal programming may be influenced or modified postnatally, for example, by the amount of nutrients given at critical times.
引用
收藏
页码:513 / 520
页数:8
相关论文
共 50 条
  • [21] Fetal programming of adipose tissue function: an evolutionary perspective
    Merkestein, Myrte
    Cagampang, Felino R.
    Sellayah, Dyan
    MAMMALIAN GENOME, 2014, 25 (9-10) : 413 - 423
  • [22] Fetal Programming of Renal Dysfunction and High Blood Pressure by Chronodisruption
    Mendez, Natalia
    Torres-Farfan, Claudia
    Salazar, Esteban
    Bascur, Pia
    Bastidas, Carla
    Vergara, Karina
    Spichiger, Carlos
    Halabi, Diego
    Vio, Carlos P.
    Richter, Hans G.
    FRONTIERS IN ENDOCRINOLOGY, 2019, 10
  • [23] Contributing Factors to Renal Dysfunction: Fetal Programming, Hormones, and Epigenetic
    Gomes, Guiomar Nascimento
    Prieto, Minolfa C.
    Thieme, Karina
    Francescato, Heloisa Della Coletta
    FRONTIERS IN PHYSIOLOGY, 2021, 12
  • [24] Abnormal renal development in a mouse model of fetal vascular programming
    Longo, M
    Lu, FX
    Snyder, R
    Anderson, G
    Hankins, G
    Saade, G
    AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2004, 191 (06) : S31 - S31
  • [25] DEVELOPMENT OF FETAL AND NEONATAL RENAL-FUNCTION
    ENGLE, WD
    SEMINARS IN PERINATOLOGY, 1986, 10 (02) : 113 - 124
  • [26] STUDIES OF RENAL FUNCTION IN INTACT FETAL LAMB
    SMITH, FG
    ADAMS, FH
    BORDEN, M
    HILBURN, J
    AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1966, 96 (02) : 240 - &
  • [27] RENAL-FUNCTION IN ADULT AND FETAL SHEEP
    HILL, KJ
    LUMBERS, ER
    JOURNAL OF DEVELOPMENTAL PHYSIOLOGY, 1988, 10 (02) : 149 - 159
  • [28] A BRIEF REVIEW OF FETAL RENAL-FUNCTION
    LUMBERS, ER
    JOURNAL OF DEVELOPMENTAL PHYSIOLOGY, 1984, 6 (01) : 1 - 10
  • [29] THE ACTIONS OF CORTISOL ON FETAL RENAL-FUNCTION
    HILL, KJ
    LUMBERS, ER
    ELBOURNE, I
    JOURNAL OF DEVELOPMENTAL PHYSIOLOGY, 1988, 10 (01) : 85 - 96
  • [30] EVALUATION OF FETAL RENAL-FUNCTION - UNRELIABILITY OF FETAL URINARY ELECTROLYTES
    ELDER, JS
    OGRADY, JP
    ASHMEAD, G
    DUCKETT, JW
    PHILIPSON, E
    JOURNAL OF UROLOGY, 1990, 144 (02): : 574 - 578