Preterm babies at risk of developing kidney disease later in life, Monash research finds
Monash University News Oct 03, 2017
Babies born prematurely could be at greater risk of developing kidney disease later in life according to a landmark Monash University study investigating the impacts of preterm birth on kidney development.
Professor Mary Jane BlackÂs team, including post-doctoral fellow Dr Megan Sutherland and PhD student Dana Vojisavljevic, from Monash UniversityÂs Biomedicine Discovery Institute, collaborated with Associate Professor Gurmeet Singh, from the Menzies School of Health Research, and Professor Wendy Hoy, from the University of Queensland on the study.
In particular, the researchers studied two common causes of prematurity - intrauterine growth restriction (IUGR), as happens when there is insufficient oxygen and nutrients being transported by the placenta to the fetus, and chorioamnionitis, on the health of the babyÂs kidneys once they are born.
As part of this study, the researchers conducted studies of renal function in term and preterm infants in the first month of life at Monash Newborn and at the Royal Darwin Hospital.
The inclusion of preterm babies born at the Royal Darwin Hospital is important, because a high proportion are Indigenous.
Eighteen percent of all Indigenous Australians have chronic kidney disease, and they are twice as likely as non-Indigenous Australians to develop the disease; they also have an increased risk of preterm birth compared to non-Indigenous Australians (14 per cent versus 9 per cent).
Professor BlackÂs research linking preterm birth and poor renal health may explain why there is an increasing incidence of kidney disease in Indigenous Australians.
ÂThis may in part be a legacy of the increased survival of preterm babies in recent decades; with preterm birth and factors associated with preterm birth, leading to changes in the kidneys that render them vulnerable to kidney disease later in life, she said.
Using animal studies, where renal development and the formation of nephrons closelyresembles that in the human, Professor Black and her collaborators have shown that impaired growth of the infant in the womb adversely impacts the number of nephrons formed in the kidneys and this can also occur, under some circumstances, following chorioamnionitis.
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Professor Mary Jane BlackÂs team, including post-doctoral fellow Dr Megan Sutherland and PhD student Dana Vojisavljevic, from Monash UniversityÂs Biomedicine Discovery Institute, collaborated with Associate Professor Gurmeet Singh, from the Menzies School of Health Research, and Professor Wendy Hoy, from the University of Queensland on the study.
In particular, the researchers studied two common causes of prematurity - intrauterine growth restriction (IUGR), as happens when there is insufficient oxygen and nutrients being transported by the placenta to the fetus, and chorioamnionitis, on the health of the babyÂs kidneys once they are born.
As part of this study, the researchers conducted studies of renal function in term and preterm infants in the first month of life at Monash Newborn and at the Royal Darwin Hospital.
The inclusion of preterm babies born at the Royal Darwin Hospital is important, because a high proportion are Indigenous.
Eighteen percent of all Indigenous Australians have chronic kidney disease, and they are twice as likely as non-Indigenous Australians to develop the disease; they also have an increased risk of preterm birth compared to non-Indigenous Australians (14 per cent versus 9 per cent).
Professor BlackÂs research linking preterm birth and poor renal health may explain why there is an increasing incidence of kidney disease in Indigenous Australians.
ÂThis may in part be a legacy of the increased survival of preterm babies in recent decades; with preterm birth and factors associated with preterm birth, leading to changes in the kidneys that render them vulnerable to kidney disease later in life, she said.
Using animal studies, where renal development and the formation of nephrons closelyresembles that in the human, Professor Black and her collaborators have shown that impaired growth of the infant in the womb adversely impacts the number of nephrons formed in the kidneys and this can also occur, under some circumstances, following chorioamnionitis.
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