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Molecular Signatures of Glomerular Neovascularization in a Patient with Diabetic Kidney Disease.

Publication ,  Journal Article
Ferkowicz, MJ; Verma, A; Barwinska, D; Melo Ferreira, R; Henderson, JM; Kirkpatrick, M; Silva, PS; Steenkamp, DW; Phillips, CL; Waikar, SS ...
Published in: Clin J Am Soc Nephrol
February 1, 2024

The Kidney Precision Medicine Project (KPMP) aims to create a kidney tissue atlas, define disease subgroups, and identify critical cells, pathways, and targets for novel therapies through molecular investigation of human kidney biopsies obtained from participants with AKI or CKD. We present the case of a 66-year-old woman with diabetic kidney disease who underwent a protocol KPMP kidney biopsy. Her clinical history included diabetes mellitus complicated by neuropathy and eye disease, increased insulin resistance, hypertension, albuminuria, and relatively preserved glomerular filtration rate (early CKD stage 3a). The patient's histopathology was consistent with diabetic nephropathy and arterial and arteriolar sclerosis. Three-dimensional, immunofluorescence imaging of the kidney biopsy specimen revealed extensive periglomerular neovascularization that was underestimated by standard histopathologic approaches. Spatial transcriptomics was performed to obtain gene expression signatures at discrete areas of the kidney biopsy. Gene expression in the areas of glomerular neovascularization revealed increased expression of genes involved in angiogenic signaling, proliferation, and survival of endothelial cells, as well as new vessel maturation and stability. This molecular correlation provides additional insights into the development of kidney disease in patients with diabetes and spotlights how novel molecular techniques used by the KPMP can supplement and enrich the histopathologic diagnosis obtained from a kidney biopsy.

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Published In

Clin J Am Soc Nephrol

DOI

EISSN

1555-905X

Publication Date

February 1, 2024

Volume

19

Issue

2

Start / End Page

266 / 275

Location

United States

Related Subject Headings

  • Urology & Nephrology
  • Transcriptome
  • Neovascularization, Pathologic
  • Kidney Glomerulus
  • Humans
  • Female
  • Diabetic Nephropathies
  • Biopsy
  • Aged
  • 4202 Epidemiology
 

Citation

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Ferkowicz, M. J., Verma, A., Barwinska, D., Melo Ferreira, R., Henderson, J. M., Kirkpatrick, M., … Kidney Precision Medicine Project, . (2024). Molecular Signatures of Glomerular Neovascularization in a Patient with Diabetic Kidney Disease. Clin J Am Soc Nephrol, 19(2), 266–275. https://doi.org/10.2215/CJN.0000000000000276
Ferkowicz, Michael J., Ashish Verma, Daria Barwinska, Ricardo Melo Ferreira, Joel M. Henderson, Mary Kirkpatrick, Paolo S. Silva, et al. “Molecular Signatures of Glomerular Neovascularization in a Patient with Diabetic Kidney Disease.Clin J Am Soc Nephrol 19, no. 2 (February 1, 2024): 266–75. https://doi.org/10.2215/CJN.0000000000000276.
Ferkowicz MJ, Verma A, Barwinska D, Melo Ferreira R, Henderson JM, Kirkpatrick M, et al. Molecular Signatures of Glomerular Neovascularization in a Patient with Diabetic Kidney Disease. Clin J Am Soc Nephrol. 2024 Feb 1;19(2):266–75.
Ferkowicz, Michael J., et al. “Molecular Signatures of Glomerular Neovascularization in a Patient with Diabetic Kidney Disease.Clin J Am Soc Nephrol, vol. 19, no. 2, Feb. 2024, pp. 266–75. Pubmed, doi:10.2215/CJN.0000000000000276.
Ferkowicz MJ, Verma A, Barwinska D, Melo Ferreira R, Henderson JM, Kirkpatrick M, Silva PS, Steenkamp DW, Phillips CL, Waikar SS, Sutton TA, Kidney Precision Medicine Project. Molecular Signatures of Glomerular Neovascularization in a Patient with Diabetic Kidney Disease. Clin J Am Soc Nephrol. 2024 Feb 1;19(2):266–275.

Published In

Clin J Am Soc Nephrol

DOI

EISSN

1555-905X

Publication Date

February 1, 2024

Volume

19

Issue

2

Start / End Page

266 / 275

Location

United States

Related Subject Headings

  • Urology & Nephrology
  • Transcriptome
  • Neovascularization, Pathologic
  • Kidney Glomerulus
  • Humans
  • Female
  • Diabetic Nephropathies
  • Biopsy
  • Aged
  • 4202 Epidemiology