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Preterm Birth Increases Susceptibility to Hyperglycemia-Induced Kidney Injury With Sex-Specific Differences in
Rachel K Dailey1, Aleksandra Cwiek2, Logan C Hamil3
1Division of Nephrology, Department of Pediatrics, University of Virginia, Charlottesville, Virginia, USA.
Insights
Preterm birth exacerbates kidney damage in diabetic female mice, but they show greater resistance to injury than males. This study highlights sex-specific differences in diabetic kidney disease progression after preterm birth.
Area of Science:
- Nephrology
- Endocrinology
- Developmental Biology
Background:
- Preterm birth is a known risk factor for diabetes and chronic kidney disease (CKD).
- The specific impact of preterm birth on the development and progression of diabetic kidney disease (DKD) remains unclear.
- Previous studies indicated male preterm mice with diabetes exhibit early DKD features, including reduced podocyte density and altered gene expression.
Purpose of the Study:
- To investigate whether preterm birth accelerates DKD progression in female mice.
- To compare structural and transcriptomic outcomes in female mice to a prior cohort of male mice to identify sex-specific differences in DKD.
- To understand the long-term renal consequences of preterm birth in the context of diabetes.
Main Methods:
- Female mice were delivered preterm (19 days post conception) or at term (20 days post conception).
- Hyperglycemia was induced using streptozotocin to create term-diabetic (T-D) and preterm-diabetic (PT-D) groups.
- Kidney tissues were analyzed using histological, stereological, imaging, and transcriptomic methods at 18 weeks.
Main Results:
- Preterm-diabetic (PT-D) females exhibited higher albuminuria, reduced proximal tubule (PT) fraction, and pro-fibrotic gene activation compared to term-nondiabetic (T-ND) females.
- PT-D females showed increased blood urea nitrogen (BUN) and a lower PT fraction than T-D females, linked to vascular pathway activation and suppressed mitochondrial metabolism.
- Sex differences included a lower PT fraction and fewer atubular glomeruli in PT-D females versus males; renin expression decreased in PT-D males but not females. Notch signaling was upregulated in both sexes.
Conclusions:
- Preterm birth sensitizes female kidneys to injury following hyperglycemia exposure.
- Despite increased susceptibility, preterm females with hyperglycemia demonstrate relative resistance to kidney damage compared to males.
- The findings reveal significant sex-specific variations in DKD progression influenced by preterm birth and hyperglycemia.
Background:
Preterm birth increases the long-term risk of diabetes and chronic kidney disease (CKD), yet its impact on diabetic kidney disease (DKD) is unclear. We previously showed that male preterm mice with diabetes develop early features of DKD, including reduced podocyte density, decreased renin expression, activation of angiogenesis pathways, and impaired endothelial-podocyte signaling. Here, we examine whether preterm birth similarly accelerates DKD progression in female mice and compare structural and transcriptomic outcomes in the females to the prior male cohort to assess sex-specific differences.
Methods:
Preterm mice were delivered by Caesarean section at 19 days post conception (dpc) and term mice at 20 dpc. Hyperglycemia was induced at 6 weeks with streptozotocin to generate term-diabetic (T-D) and preterm-diabetic (PT-D) groups; controls were term-nondiabetic (T-ND) and preterm-nondiabetic (PT-ND). Body weight and glucose were monitored, and kidneys were analyzed at 18 weeks using histologic, stereologic, imaging, and transcriptomic methods.
Results:
Compared with T-ND females, PT-D females showed higher albuminuria, more atubular glomeruli, reduced proximal tubule (PT) fraction, and pro-fibrotic gene activation. Compared to T-D females, PT-D females had higher blood urea nitrogen (BUN) levels and reduced PT fraction. This was associated with activation of pathways associated with the vasculature and suppression of mitochondrial metabolism gene pathways, along with Notch signalling alterations. Sex differences included a lower PT fraction in preterm females than males and fewer atubular glomeruli in PT-D females than PT-D males. Renin expression was lower in PT-D than T-D in males only. When comparing PT-D to T-D across sexes, 582 differentially expressed genes were unique to females. Notch signalling was upregulated in both male and female PT-D mice compared to T-D.
Conclusion:
Preterm birth increases susceptibility to kidney injury in females after exposure to hyperglycemia. However, preterm females with hyperglycemia are more resistant to kidney damage than males.
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