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.
Abstract

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