Noninvasive Evaluation of Renal Hypoxia by Multiparametric Functional MRI in Early Diabetic Kidney Disease

Background Renal hypoxia, which caused by a mismatch between oxygen delivery and oxygen demand, may be the primary pathophysiological pathway driving diabetic kidney disease (DKD). Blood oxygenation level‐dependent (BOLD) magnetic resonance imaging (MRI) could detect hypoxia, but can be limited in d...

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Published inJournal of magnetic resonance imaging Vol. 55; no. 2; pp. 518 - 527
Main Authors Wang, Rui, Lin, Zhiyong, Yang, Xuedong, Zhao, Kai, Wang, Suxia, Sui, Xueqing, Su, Tao, Wang, Xiaoying
Format Journal Article
LanguageEnglish
Published Hoboken, USA John Wiley & Sons, Inc 01.02.2022
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Abstract Background Renal hypoxia, which caused by a mismatch between oxygen delivery and oxygen demand, may be the primary pathophysiological pathway driving diabetic kidney disease (DKD). Blood oxygenation level‐dependent (BOLD) magnetic resonance imaging (MRI) could detect hypoxia, but can be limited in distinguishing increased oxygen consumption or decreased blood supply. Purpose To explore multiparametric functional MRI in evaluating mechanism of the hypoxia changes in early stage of DKD. Study Type Prospective. Animal Model Thirty‐five New Zealand White rabbits were divided into control group (n = 5) and alloxan‐induced diabetes mellitus (DM) groups (DM3 group: n = 15, DM7 group: n = 15). Field Strength/Sequence 3 T MRI/BOLD, arterial spin labeling (ASL), and asymmetric spin‐echo (ASE). Assessment The renal oxygenation level (R2*), renal blood flow (RBF), and oxygen extraction fraction (OEF) were evaluated by BOLD, ASL, and ASE MRI, respectively. The regions of interest were manually drawn including cortex, outer stripes of outer medulla (OS), and inner stripes of outer medulla (IS). Statistical Tests Analysis of variance, independent‐sample t‐test, and paired‐sample t‐test were applied for comparisons among groups, between groups, and within the same group. P < 0.05 was considered statistically significant. Results All renal regions of DM3 group at Day 3 after DM induction showed significantly higher R2* and OEF values compared to baseline. The RBF values showed no statistically significant difference (P = 0.62, 0.76, 0.09 in cortex, OS, and IS, respectively). For DM7 group at Day 7, R2*, OEF, and RBF values showed no statistically significant difference compared to baseline (P = 0.06, 0.05, 0.06 of R2*; 0.70, 0.64, 0.68 of OEF; and 0.33, 0.58, 0.48 of RBF in cortex, OS, and IS, respectively). Data Conclusion BOLD MRI could detect renal hypoxia in early stage of DKD rabbit model, which was mainly revealed by increased oxygen consumption, but not affected by renal blood flow change. Level of Evidence: 2 Technical Efficacy Stage: 1
AbstractList Renal hypoxia, which caused by a mismatch between oxygen delivery and oxygen demand, may be the primary pathophysiological pathway driving diabetic kidney disease (DKD). Blood oxygenation level-dependent (BOLD) magnetic resonance imaging (MRI) could detect hypoxia, but can be limited in distinguishing increased oxygen consumption or decreased blood supply. To explore multiparametric functional MRI in evaluating mechanism of the hypoxia changes in early stage of DKD. Prospective. Thirty-five New Zealand White rabbits were divided into control group (n = 5) and alloxan-induced diabetes mellitus (DM) groups (DM3 group: n = 15, DM7 group: n = 15). 3 T MRI/BOLD, arterial spin labeling (ASL), and asymmetric spin-echo (ASE). The renal oxygenation level (R2*), renal blood flow (RBF), and oxygen extraction fraction (OEF) were evaluated by BOLD, ASL, and ASE MRI, respectively. The regions of interest were manually drawn including cortex, outer stripes of outer medulla (OS), and inner stripes of outer medulla (IS). Analysis of variance, independent-sample t-test, and paired-sample t-test were applied for comparisons among groups, between groups, and within the same group. P < 0.05 was considered statistically significant. All renal regions of DM3 group at Day 3 after DM induction showed significantly higher R2* and OEF values compared to baseline. The RBF values showed no statistically significant difference (P = 0.62, 0.76, 0.09 in cortex, OS, and IS, respectively). For DM7 group at Day 7, R2*, OEF, and RBF values showed no statistically significant difference compared to baseline (P = 0.06, 0.05, 0.06 of R2*; 0.70, 0.64, 0.68 of OEF; and 0.33, 0.58, 0.48 of RBF in cortex, OS, and IS, respectively). BOLD MRI could detect renal hypoxia in early stage of DKD rabbit model, which was mainly revealed by increased oxygen consumption, but not affected by renal blood flow change. 2 Technical Efficacy Stage: 1.
BackgroundRenal hypoxia, which caused by a mismatch between oxygen delivery and oxygen demand, may be the primary pathophysiological pathway driving diabetic kidney disease (DKD). Blood oxygenation level‐dependent (BOLD) magnetic resonance imaging (MRI) could detect hypoxia, but can be limited in distinguishing increased oxygen consumption or decreased blood supply.PurposeTo explore multiparametric functional MRI in evaluating mechanism of the hypoxia changes in early stage of DKD.Study TypeProspective.Animal ModelThirty‐five New Zealand White rabbits were divided into control group (n = 5) and alloxan‐induced diabetes mellitus (DM) groups (DM3 group: n = 15, DM7 group: n = 15).Field Strength/Sequence3 T MRI/BOLD, arterial spin labeling (ASL), and asymmetric spin‐echo (ASE).AssessmentThe renal oxygenation level (R2*), renal blood flow (RBF), and oxygen extraction fraction (OEF) were evaluated by BOLD, ASL, and ASE MRI, respectively. The regions of interest were manually drawn including cortex, outer stripes of outer medulla (OS), and inner stripes of outer medulla (IS).Statistical TestsAnalysis of variance, independent‐sample t‐test, and paired‐sample t‐test were applied for comparisons among groups, between groups, and within the same group. P < 0.05 was considered statistically significant.ResultsAll renal regions of DM3 group at Day 3 after DM induction showed significantly higher R2* and OEF values compared to baseline. The RBF values showed no statistically significant difference (P = 0.62, 0.76, 0.09 in cortex, OS, and IS, respectively). For DM7 group at Day 7, R2*, OEF, and RBF values showed no statistically significant difference compared to baseline (P = 0.06, 0.05, 0.06 of R2*; 0.70, 0.64, 0.68 of OEF; and 0.33, 0.58, 0.48 of RBF in cortex, OS, and IS, respectively).Data ConclusionBOLD MRI could detect renal hypoxia in early stage of DKD rabbit model, which was mainly revealed by increased oxygen consumption, but not affected by renal blood flow change.Level of Evidence: 2Technical Efficacy Stage: 1
Renal hypoxia, which caused by a mismatch between oxygen delivery and oxygen demand, may be the primary pathophysiological pathway driving diabetic kidney disease (DKD). Blood oxygenation level-dependent (BOLD) magnetic resonance imaging (MRI) could detect hypoxia, but can be limited in distinguishing increased oxygen consumption or decreased blood supply.BACKGROUNDRenal hypoxia, which caused by a mismatch between oxygen delivery and oxygen demand, may be the primary pathophysiological pathway driving diabetic kidney disease (DKD). Blood oxygenation level-dependent (BOLD) magnetic resonance imaging (MRI) could detect hypoxia, but can be limited in distinguishing increased oxygen consumption or decreased blood supply.To explore multiparametric functional MRI in evaluating mechanism of the hypoxia changes in early stage of DKD.PURPOSETo explore multiparametric functional MRI in evaluating mechanism of the hypoxia changes in early stage of DKD.Prospective.STUDY TYPEProspective.Thirty-five New Zealand White rabbits were divided into control group (n = 5) and alloxan-induced diabetes mellitus (DM) groups (DM3 group: n = 15, DM7 group: n = 15).ANIMAL MODELThirty-five New Zealand White rabbits were divided into control group (n = 5) and alloxan-induced diabetes mellitus (DM) groups (DM3 group: n = 15, DM7 group: n = 15).3 T MRI/BOLD, arterial spin labeling (ASL), and asymmetric spin-echo (ASE).FIELD STRENGTH/SEQUENCE3 T MRI/BOLD, arterial spin labeling (ASL), and asymmetric spin-echo (ASE).The renal oxygenation level (R2*), renal blood flow (RBF), and oxygen extraction fraction (OEF) were evaluated by BOLD, ASL, and ASE MRI, respectively. The regions of interest were manually drawn including cortex, outer stripes of outer medulla (OS), and inner stripes of outer medulla (IS).ASSESSMENTThe renal oxygenation level (R2*), renal blood flow (RBF), and oxygen extraction fraction (OEF) were evaluated by BOLD, ASL, and ASE MRI, respectively. The regions of interest were manually drawn including cortex, outer stripes of outer medulla (OS), and inner stripes of outer medulla (IS).Analysis of variance, independent-sample t-test, and paired-sample t-test were applied for comparisons among groups, between groups, and within the same group. P < 0.05 was considered statistically significant.STATISTICAL TESTSAnalysis of variance, independent-sample t-test, and paired-sample t-test were applied for comparisons among groups, between groups, and within the same group. P < 0.05 was considered statistically significant.All renal regions of DM3 group at Day 3 after DM induction showed significantly higher R2* and OEF values compared to baseline. The RBF values showed no statistically significant difference (P = 0.62, 0.76, 0.09 in cortex, OS, and IS, respectively). For DM7 group at Day 7, R2*, OEF, and RBF values showed no statistically significant difference compared to baseline (P = 0.06, 0.05, 0.06 of R2*; 0.70, 0.64, 0.68 of OEF; and 0.33, 0.58, 0.48 of RBF in cortex, OS, and IS, respectively).RESULTSAll renal regions of DM3 group at Day 3 after DM induction showed significantly higher R2* and OEF values compared to baseline. The RBF values showed no statistically significant difference (P = 0.62, 0.76, 0.09 in cortex, OS, and IS, respectively). For DM7 group at Day 7, R2*, OEF, and RBF values showed no statistically significant difference compared to baseline (P = 0.06, 0.05, 0.06 of R2*; 0.70, 0.64, 0.68 of OEF; and 0.33, 0.58, 0.48 of RBF in cortex, OS, and IS, respectively).BOLD MRI could detect renal hypoxia in early stage of DKD rabbit model, which was mainly revealed by increased oxygen consumption, but not affected by renal blood flow change.DATA CONCLUSIONBOLD MRI could detect renal hypoxia in early stage of DKD rabbit model, which was mainly revealed by increased oxygen consumption, but not affected by renal blood flow change.2 Technical Efficacy Stage: 1.LEVEL OF EVIDENCE2 Technical Efficacy Stage: 1.
Background Renal hypoxia, which caused by a mismatch between oxygen delivery and oxygen demand, may be the primary pathophysiological pathway driving diabetic kidney disease (DKD). Blood oxygenation level‐dependent (BOLD) magnetic resonance imaging (MRI) could detect hypoxia, but can be limited in distinguishing increased oxygen consumption or decreased blood supply. Purpose To explore multiparametric functional MRI in evaluating mechanism of the hypoxia changes in early stage of DKD. Study Type Prospective. Animal Model Thirty‐five New Zealand White rabbits were divided into control group (n = 5) and alloxan‐induced diabetes mellitus (DM) groups (DM3 group: n = 15, DM7 group: n = 15). Field Strength/Sequence 3 T MRI/BOLD, arterial spin labeling (ASL), and asymmetric spin‐echo (ASE). Assessment The renal oxygenation level (R2*), renal blood flow (RBF), and oxygen extraction fraction (OEF) were evaluated by BOLD, ASL, and ASE MRI, respectively. The regions of interest were manually drawn including cortex, outer stripes of outer medulla (OS), and inner stripes of outer medulla (IS). Statistical Tests Analysis of variance, independent‐sample t‐test, and paired‐sample t‐test were applied for comparisons among groups, between groups, and within the same group. P < 0.05 was considered statistically significant. Results All renal regions of DM3 group at Day 3 after DM induction showed significantly higher R2* and OEF values compared to baseline. The RBF values showed no statistically significant difference (P = 0.62, 0.76, 0.09 in cortex, OS, and IS, respectively). For DM7 group at Day 7, R2*, OEF, and RBF values showed no statistically significant difference compared to baseline (P = 0.06, 0.05, 0.06 of R2*; 0.70, 0.64, 0.68 of OEF; and 0.33, 0.58, 0.48 of RBF in cortex, OS, and IS, respectively). Data Conclusion BOLD MRI could detect renal hypoxia in early stage of DKD rabbit model, which was mainly revealed by increased oxygen consumption, but not affected by renal blood flow change. Level of Evidence: 2 Technical Efficacy Stage: 1
Author Wang, Suxia
Su, Tao
Wang, Xiaoying
Yang, Xuedong
Zhao, Kai
Sui, Xueqing
Wang, Rui
Lin, Zhiyong
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Keywords blood oxygenation level-dependent MRI
diabetic kidney disease
hypoxia
oxygen extraction fraction
arterial spin labeling
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Snippet Background Renal hypoxia, which caused by a mismatch between oxygen delivery and oxygen demand, may be the primary pathophysiological pathway driving diabetic...
Renal hypoxia, which caused by a mismatch between oxygen delivery and oxygen demand, may be the primary pathophysiological pathway driving diabetic kidney...
BackgroundRenal hypoxia, which caused by a mismatch between oxygen delivery and oxygen demand, may be the primary pathophysiological pathway driving diabetic...
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StartPage 518
SubjectTerms Alloxan
Animal models
Animals
arterial spin labeling
Blood flow
blood oxygenation level‐dependent MRI
Diabetes
Diabetes Mellitus
diabetic kidney disease
Diabetic Nephropathies - diagnostic imaging
Diabetic nephropathy
Evaluation
Field strength
Functional magnetic resonance imaging
Hypoxia
Hypoxia - diagnostic imaging
Kidney - diagnostic imaging
Kidney diseases
Kidneys
Magnetic Resonance Imaging
Neuroimaging
Noninvasive evaluation
Oxygen
Oxygen consumption
Oxygen demand
oxygen extraction fraction
Oxygenation
Prospective Studies
Rabbits
Renal cortex
Spin labeling
Statistical analysis
Statistical tests
Variance analysis
Title Noninvasive Evaluation of Renal Hypoxia by Multiparametric Functional MRI in Early Diabetic Kidney Disease
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjmri.27814
https://www.ncbi.nlm.nih.gov/pubmed/34184356
https://www.proquest.com/docview/2620935756
https://www.proquest.com/docview/2546598363
Volume 55
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