13 research outputs found

    Baseline clinical and pathological data of the artery wall in kidney transplant patients according to carotid intima-media thickness tertiles.

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    <p>Abbreviations: c-IMT, carotid intima-media thickness; CKD, chronic kidney disease; ACEI/ARA, angiotensin-converting enzyme inhibitor/angiotensin receptor antagonist; IEA, inferior epigastric artery.</p><p><sup>a</sup><i>P</i><0.0001 vs. T2 and T1;</p><p><sup>b</sup><i>P</i><0.0001 vs. T1;</p><p><sup>c</sup><i>P</i> = 0.033 vs T2;</p><p><sup>d</sup><i>P</i> = 0.012 vs. T1;</p><p><sup>e</sup><i>P</i> = 0.006 vs. T1;</p><p><sup>f</sup><i>P</i> = 0.023 vs. T1;</p><p><sup>g</sup><i>P</i> = 0.001</p><p>Baseline clinical and pathological data of the artery wall in kidney transplant patients according to carotid intima-media thickness tertiles.</p

    Artery Wall Assessment Helps Predict Kidney Transplant Outcome

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    <div><p>Background</p><p>Kidney transplant recipients have high cardiovascular risk, and vascular inflammation may play an important role. We explored whether the inflammatory state in the vessel wall was related to carotid intima-media thickness (c-IMT) and patient survival following kidney transplantation.</p><p>Methods</p><p>In this prospective observational cohort study we measured c-IMT and expression of proinflammatory cytokines and adhesion molecules in the inferior epigastric artery in 115 kidney transplant candidates. Another c-IMT measurement was done 1-year post-transplantation in 107. By stepwise multiple regression analysis we explored factors associated with baseline c-IMT and their changes over time. Multivariate Cox regression analysis was constructed to identify risk factors for mortality.</p><p>Results</p><p>A worse cardiovascular profile (older age, smoker, diabetic, carotid plaque, systolic blood pressure and vascular calcification) and higher VCAM-1 levels were found in patients in the highest baseline c-IMT tertile, who also had a worse survival. Factors independently related to baseline c-IMT were age (β=0.369, <i>P</i><0.0001), fasting glucose (β=0.168, <i>P</i>=0.045), smoking (β=0.228, <i>P</i>=0.003) and VCAM-1 levels (β=0.244, <i>P</i>=0.002). Independent factors associated with c-IMT measurement 1-year post-transplantation were baseline c-IMT (β=-0.677, <i>P</i><0.0001), post-transplant diabetes (β=0.225, <i>P</i>=0.003) and triglycerides (β=0.302, <i>P</i>=0.023). Vascular VCAM-1 levels were associated with increased risk of mortality in bivariate and multivariate Cox regression. Notably, nearly 50% of patients showed an increase or maintenance of high c-IMT 1 year post-transplantation and these patients experienced a higher mortality (13 versus 3.5%; <i>P</i>=0.021).</p><p>Conclusion</p><p>A worse cardiovascular profile and a higher vascular VCAM-1 protein levels at time of KT are related to subclinical atheromatosis. This could lead to a higher post-transplant mortality. Pre-transplant c IMT, post-transplant diabetes and triglycerides at 1-year post-transplantation may condition a high c-IMT measurement post-transplantation, which may decrease patient survival.</p></div

    Clinical characteristics of patients after stratification according to c-IMT measurement variation after second carotid echographic study.

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    <p>Abbreviations: c-IMT, carotid intima-media thickness; CVD, cardiovascular disease; KT, kidney transplantation; ACEI/ARA, angiotensin-converting enzyme inhibitor/angiotensin receptor antagonist; NODAT, new onset diabetes after transplantation.</p><p>Clinical characteristics of patients after stratification according to c-IMT measurement variation after second carotid echographic study.</p

    Proinflammatory cytokines, adhesion molecules and c-IMT measurements.

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    <p>A) Differences in the gene expression of proinflammatory markers in the artery wall according to c-IMT tertiles. B) Differences in the quantification of proinflammatory proteins by c-IMT tertiles. *ANOVA test for VCAM-1, <i>P</i> = 0.003; Bonferroni procedure, T3 vs. T1, p = 0.003; T3 vs T2, <i>P</i> = 0.076.</p

    Relationship between VCAM protein levels and overall mortality by bivariate and multivariate Cox regression analysis

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    <p>Abbreviations: c-IMT, carotid intima-media thickness; KT, kidney transplantation; VC, vascular calcifications; NODAT, new onset diabetes after transplantation; PD, peritoneal dialysis; T-cholesterol, total cholesterol. Group II, patients who showed an increase to the highest tertile or who maintained both values within the highest tertile; Group I, patients who showed a reduction to a lower tertile or who maintained both values within the lower or the middle tertile.</p><p>*Because the number of events was few, this analysis was performed entering risk factors two by two.</p><p>Relationship between VCAM protein levels and overall mortality by bivariate and multivariate Cox regression analysis</p

    Kaplan-Meier curves according to variation patterns between the c-IMT tertiles at both time periods.

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    <p>Solid line indicates the “decrease or stable low-middle” group and dotted line the “increase or stable high” group (log-rank analysis 5.4; <i>P</i> = 0.021).</p

    Baseline clinical and pathological data of the artery wall in kidney transplant candidates according to VCAM-1 protein level tertiles.

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    <p>Abbreviations: c-IMT, carotid intima-media thickness; CKD, chronic kidney disease; ACEI/ARA, angiotensin-converting enzyme inhibitor/angiotensin receptor antagonist; IEA, inferior epigastric artery.</p><p><sup>a</sup><i>P</i><0.0001 vs. T2 and T1;</p><p><sup>b</sup><i>P</i><0.0001 vs. T1 and T3;</p><p><sup>c</sup><i>P</i> = 0.001 vs. T1;</p><p><sup>d</sup><i>P</i> = 0.010 vs. T3;</p><p><sup>e</sup><i>P</i> = 0.042 vs. T2;</p><p><sup>f</sup><i>P</i> = 0.054 vs. T1;</p><p><sup>g</sup><i>P</i> = 0.016 vs. T1;</p><p><sup>h</sup><i>P</i><0.0001 vs. T1;</p><p><sup>i</sup><i>P</i> = 0.002 vs. T3.</p><p>Baseline clinical and pathological data of the artery wall in kidney transplant candidates according to VCAM-1 protein level tertiles.</p
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