Attenuated kidney oxidative metabolism in young adults with type 1 diabetes

BACKGROUNDIn type 1 diabetes (T1D), impaired insulin sensitivity may contribute to the development of diabetic kidney disease (DKD) through alterations in kidney oxidative metabolism.METHODSYoung adults with T1D (n = 30) and healthy controls (HCs) (n = 20) underwent hyperinsulinemic-euglycemic clamp studies, MRI, 11C-acetate PET, kidney biopsies, single-cell RNA-Seq, and spatial metabolomics to assess this relationship.RESULTSParticipants with T1D had significantly higher glomerular basement membrane (GBM) thickness compared with HCs. T1D participants exhibited lower insulin sensitivity and cortical oxidative metabolism, correlating with higher insulin sensitivity. Proximal tubular transcripts of TCA cycle and oxidative phosphorylation enzymes were lower in T1D. Spatial metabolomics showed reductions in tubular TCA cycle intermediates, indicating mitochondrial dysfunction. The Slingshot algorithm identified a lineage of proximal tubular cells progressing from stable to adaptive/maladaptive subtypes, using pseudotime trajectory analysis, which computationally orders cells along a continuum of states. This analysis revealed distinct distribution patterns between T1D and HCs, with attenuated oxidative metabolism in T1D attributed to a greater proportion of adaptive/maladaptive subtypes with low expression of TCA cycle and oxidative phosphorylation transcripts. Pseudotime progression associated with higher HbA1c, BMI, and GBM, and lower insulin sensitivity and cortical oxidative metabolism.CONCLUSIONThese early structural and metabolic changes in T1D kidneys may precede clinical DKD.TRIAL REGISTRATIONClinicalTrials.gov NCT04074668.FUNDINGUniversity of Michigan O'Brien Kidney Translational Core Center grant (P30 DK081943); CROCODILE studies by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) (P30 DK116073), Juvenile Diabetes Research Foundation (JDRF) (2-SRA-2019-845-S-B), Boettcher Foundation, Intramural Research Program at NIDDK and Centers for Disease Control and Prevention (CKD Initiative) under Inter-Agency Agreement #21FED2100157DPG.

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Journal
Journal of Clinical Investigation
Published
2024-10-22
DOI
https://doi.org/10.1172/jci183984
Citations
6
Primary Topic
Diabetes and associated disorders
Type
article
Field-Weighted Citation Impact
3.30

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article

Attenuated kidney oxidative metabolism in young adults with type 1 diabetes

Frank C. Brosius, Kristen J. Nadeau, Bennett B. Chin, Kelly Street et al.
6 citations
Journal of Clinical Investigation
Diabetes and associated disorders
3.30
article

Attenuated kidney oxidative metabolism in young adults with type 1 diabetes

Frank C. Brosius, Kristen J. Nadeau, Bennett B. Chin, Kelly Street, Gabriel Richard, Tim Vigers, Pierre‐Jean Saulnier, Carissa Birznieks, Denis P. Blondin, Viji Nair, Jennifer A. Schaub, Viral N. Shah, Fadhl Alakwaa, Phillip J. McCown, Ye Ji Choi, Ian H. de Boer, Phoom Narongkiatikhun, Petter Bjornstad, Victor G. Puelles, Pottumarthi Prasad, Jesse A. Goodrich, Laura L. Pyle, Janet K. Snell‐Bergeon, Edgar A. Otto, B Gurung, Daniël H. van Raalte, Abhijit S. Naik, Guanshi Zhang, Kalie L. Tommerdahl, Matthias Kretzler, Jessica Kendrick, Patricia Ladd, Maureen Flynn, Jeffrey B. Hodgin, Robert G. Nelson, Kumar Sharma, Yingbao Yang, Luping Li, Ian M. Tamayo, Lynette Driscoll, Dawit Demeke, David Z. Cherney, Manjeri A. Venkatachalam, A. López Ruiz, Alexis MacDonald, Susan J. Gross
article en
6 citations

Abstract

BACKGROUNDIn type 1 diabetes (T1D), impaired insulin sensitivity may contribute to the development of diabetic kidney disease (DKD) through alterations in kidney oxidative metabolism.METHODSYoung adults with T1D (n = 30) and healthy controls (HCs) (n = 20) underwent hyperinsulinemic-euglycemic clamp studies, MRI, 11C-acetate PET, kidney biopsies, single-cell RNA-Seq, and spatial metabolomics to assess this relationship.RESULTSParticipants with T1D had significantly higher glomerular basement membrane (GBM) thickness compared with HCs. T1D participants exhibited lower insulin sensitivity and cortical oxidative metabolism, correlating with higher insulin sensitivity. Proximal tubular transcripts of TCA cycle and oxidative phosphorylation enzymes were lower in T1D. Spatial metabolomics showed reductions in tubular TCA cycle intermediates, indicating mitochondrial dysfunction. The Slingshot algorithm identified a lineage of proximal tubular cells progressing from stable to adaptive/maladaptive subtypes, using pseudotime trajectory analysis, which computationally orders cells along a continuum of states. This analysis revealed distinct distribution patterns between T1D and HCs, with attenuated oxidative metabolism in T1D attributed to a greater proportion of adaptive/maladaptive subtypes with low expression of TCA cycle and oxidative phosphorylation transcripts. Pseudotime progression associated with higher HbA1c, BMI, and GBM, and lower insulin sensitivity and cortical oxidative metabolism.CONCLUSIONThese early structural and metabolic changes in T1D kidneys may precede clinical DKD.TRIAL REGISTRATIONClinicalTrials.gov NCT04074668.FUNDINGUniversity of Michigan O'Brien Kidney Translational Core Center grant (P30 DK081943); CROCODILE studies by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) (P30 DK116073), Juvenile Diabetes Research Foundation (JDRF) (2-SRA-2019-845-S-B), Boettcher Foundation, Intramural Research Program at NIDDK and Centers for Disease Control and Prevention (CKD Initiative) under Inter-Agency Agreement #21FED2100157DPG.

Journal of Clinical InvestigationVol. 134(24)
University of Southern California (US), Université de Sherbrooke (CA), University of Arizona (US), Inserm (FR), Universität Hamburg (DE), The University of Texas at San Antonio Health Science Center (US), University of Toronto (CA), University of Washington (US), Aarhus University (DK), University of Michigan (US), Centre Hospitalier Universitaire de Sherbrooke (CA), Aarhus University Hospital (DK), Université de Poitiers (FR), University of Chicago (US), National Institute of Diabetes and Digestive and Kidney Diseases (US), University Medical Center Hamburg-Eppendorf (DE), Centre Hospitalier Universitaire de Poitiers (FR), Sylvana Research (US), Institute of Population and Public Health (CA), Amsterdam University Medical Centers (NL), The University of Texas at San Antonio (US), University of Colorado Anschutz Medical Campus (US), Seattle University (US), University of Colorado Denver (US)
American Heart Association, Boettcher Foundation, University of Michigan, Centers for Disease Control and Prevention, National Institute of Diabetes and Digestive and Kidney Diseases
Zero hunger
Openalex Percentile: Top 8%
Diabetes and associated disorders
3.30
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