Programming of Renal Development and Chronic Disease in Adult Life

Eugenie R Lumbers; Yoga Kandasamy; Sarah J Delforce; Amanda C Boyce; Karen J Gibson; Kirsty G Pringle

doi:10.3389/fphys.2020.00757

Programming of Renal Development and Chronic Disease in Adult Life

Front Physiol. 2020 Jul 16:11:757. doi: 10.3389/fphys.2020.00757. eCollection 2020.

Authors

Eugenie R Lumbers^{1

2}, Yoga Kandasamy^{1

2

3}, Sarah J Delforce^{1

2}, Amanda C Boyce⁴, Karen J Gibson⁴, Kirsty G Pringle^{1

2}

Affiliations

¹ School of Biomedical Sciences and Pharmacy, Faculty of Health and Medicine, The University of Newcastle, Callaghan, NSW, Australia.
² Hunter Medical Research Institute, Newcastle, NSW, Australia.
³ Department of Neonatology, Townsville University Hospital, Douglas, QLD, Australia.
⁴ School of Medical Sciences, University of New South Wales, Sydney, NSW, Australia.

Abstract

Chronic kidney disease (CKD) can have an insidious onset because there is a gradual decline in nephron number throughout life. There may be no overt symptoms of renal dysfunction until about two thirds or more of the nephrons have been destroyed and glomerular filtration rate (GFR) falls to below 25% of normal (often in mid-late life) (Martinez-Maldonaldo et al., 1992). Once End Stage Renal Disease (ESRD) has been reached, survival depends on renal replacement therapy (RRT). CKD causes hypertension and cardiovascular disease; and hypertension causes CKD. Albuminuria is also a risk factor for cardiovascular disease. The age of onset of CKD is partly determined during fetal life. This review describes the mechanisms underlying the development of CKD in adult life that results from abnormal renal development caused by an adverse intrauterine environment. The basis of this form of CKD is thought to be mainly due to a reduction in the number of nephrons formed in utero which impacts on the age dependent decline in glomerular function. Factors that affect the risk of reduced nephron formation during intrauterine life are discussed and include maternal nutrition (malnutrition and obesity, micronutrients), smoking and alcohol, use of drugs that block the maternal renin-angiotensin system, glucocorticoid excess and maternal renal dysfunction and prematurity. Since CKD, hypertension and cardiovascular disease add to the disease burden in the community we recommend that kidney size at birth should be recorded using ultrasound and those individuals who are born premature or who have small kidneys at this time should be monitored regularly by determining GFR and albumin:creatinine clearance ratio. Furthermore, public health measures aimed at limiting the prevalence of obesity and diabetes mellitus as well as providing advice on limiting the amount of protein ingested during a single meal, because they are all associated with increased glomerular hyperfiltration and subsequent glomerulosclerosis would be beneficial.

Keywords: development; glomerular hypertension; nutrition; oligonephropathy; renal; renin.

Publication types

Review