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Advanced glycation end products (AGEs) estimated by skin autofluorescence are related with cardiovascular risk in renal transplant

BACKGROUND: Advanced glycation end products (AGEs) accumulation, a measure of cumulative metabolic stress, constitute a novel pathogenic mechanism involved in aging, diabetes, cardiovascular (CVD) and chronic kidney disease (CKD). Despite removal of uremic toxins and AGEs after a successful renal tr...

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Autores principales: Calviño, Jesus, Cigarran, Secundino, Gonzalez-Tabares, Lourdes, Menendez, Nicolas, Latorre, Juan, Cillero, Sonia, Millan, Beatriz, Cobelo, Carmen, Sanjurjo-Amado, Ana, Quispe, Jansen, Garcia-Enriquez, Alba, Carrero, Juan J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6070236/
https://www.ncbi.nlm.nih.gov/pubmed/30067789
http://dx.doi.org/10.1371/journal.pone.0201118
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author Calviño, Jesus
Cigarran, Secundino
Gonzalez-Tabares, Lourdes
Menendez, Nicolas
Latorre, Juan
Cillero, Sonia
Millan, Beatriz
Cobelo, Carmen
Sanjurjo-Amado, Ana
Quispe, Jansen
Garcia-Enriquez, Alba
Carrero, Juan J.
author_facet Calviño, Jesus
Cigarran, Secundino
Gonzalez-Tabares, Lourdes
Menendez, Nicolas
Latorre, Juan
Cillero, Sonia
Millan, Beatriz
Cobelo, Carmen
Sanjurjo-Amado, Ana
Quispe, Jansen
Garcia-Enriquez, Alba
Carrero, Juan J.
author_sort Calviño, Jesus
collection PubMed
description BACKGROUND: Advanced glycation end products (AGEs) accumulation, a measure of cumulative metabolic stress, constitute a novel pathogenic mechanism involved in aging, diabetes, cardiovascular (CVD) and chronic kidney disease (CKD). Despite removal of uremic toxins and AGEs after a successful renal transplant (RT), CVD remains the leading cause of mortality. We hypothesized that AGEs measurement by Skin Autofluorescence (SAF) might be useful even after a successful RT and thus reflect the high cardiovascular risk burden of these patients. METHODS: 189 stable RT (61% men, aged 56±13.0 years), CKD stages 1–4 and >12 months since RT were enrolled. Variables collected comprised comorbid history, medication use, smoking habit, routine biochemistry, subclinical atheromatosis by ankle-brachial-index (ABI) and allograft resistivity index (RI), 24-h ABPM, anthropometry and handgrip strength. AGEs were measured by SAF and expressed in arbitrary units (AU). Vascular age was estimated by Koetsier´s formula (SAF-0.83/0.024) and expected 10-years cardiovascular death risk was calculated with the REGICOR score. RESULTS: Mean SAF was 3.00±0.83 AU and estimated vascular age 90±34.7 years (30 years above biological age). SAF was higher among men (3.10±0.91 vs 2.81±0.66), diabetic nephropathy (3.49±0.75 vs 2.96±0.83) and steroid users (3.14±0.86 vs 2.71±0.69). We observed a positive correlation of SAF with night-systolic blood pressure (r = 0.25, p = 0.001), parathormone (r = 0.20, p<0.01), phosphate (r = 0.28, p<0.001) and negative with hemoglobin (r = -0.29, p<0.001), CKD-EPI (r = -0.32, p<0.001), albumin (r = -0.17, p<0.05), and dynamometry (r = -0.20, p<0.01). Subclinical vascular atheromatosis (ABI and RI) as well as the REGICOR scale (r = 0.35 p<0.001) were also correlated with SAF. In multivariable analysis age, gender, steroid use, serum phosphate and handgrip strength remained independently associated with SAF. CONCLUSIONS: SAF levels are elevated in RT patients and correlate with CVD risk. Besides age and male sex, our results suggest that phosphate overload, steroid use and nutritional status are important factors linking to AGEs accumulation.
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spelling pubmed-60702362018-08-09 Advanced glycation end products (AGEs) estimated by skin autofluorescence are related with cardiovascular risk in renal transplant Calviño, Jesus Cigarran, Secundino Gonzalez-Tabares, Lourdes Menendez, Nicolas Latorre, Juan Cillero, Sonia Millan, Beatriz Cobelo, Carmen Sanjurjo-Amado, Ana Quispe, Jansen Garcia-Enriquez, Alba Carrero, Juan J. PLoS One Research Article BACKGROUND: Advanced glycation end products (AGEs) accumulation, a measure of cumulative metabolic stress, constitute a novel pathogenic mechanism involved in aging, diabetes, cardiovascular (CVD) and chronic kidney disease (CKD). Despite removal of uremic toxins and AGEs after a successful renal transplant (RT), CVD remains the leading cause of mortality. We hypothesized that AGEs measurement by Skin Autofluorescence (SAF) might be useful even after a successful RT and thus reflect the high cardiovascular risk burden of these patients. METHODS: 189 stable RT (61% men, aged 56±13.0 years), CKD stages 1–4 and >12 months since RT were enrolled. Variables collected comprised comorbid history, medication use, smoking habit, routine biochemistry, subclinical atheromatosis by ankle-brachial-index (ABI) and allograft resistivity index (RI), 24-h ABPM, anthropometry and handgrip strength. AGEs were measured by SAF and expressed in arbitrary units (AU). Vascular age was estimated by Koetsier´s formula (SAF-0.83/0.024) and expected 10-years cardiovascular death risk was calculated with the REGICOR score. RESULTS: Mean SAF was 3.00±0.83 AU and estimated vascular age 90±34.7 years (30 years above biological age). SAF was higher among men (3.10±0.91 vs 2.81±0.66), diabetic nephropathy (3.49±0.75 vs 2.96±0.83) and steroid users (3.14±0.86 vs 2.71±0.69). We observed a positive correlation of SAF with night-systolic blood pressure (r = 0.25, p = 0.001), parathormone (r = 0.20, p<0.01), phosphate (r = 0.28, p<0.001) and negative with hemoglobin (r = -0.29, p<0.001), CKD-EPI (r = -0.32, p<0.001), albumin (r = -0.17, p<0.05), and dynamometry (r = -0.20, p<0.01). Subclinical vascular atheromatosis (ABI and RI) as well as the REGICOR scale (r = 0.35 p<0.001) were also correlated with SAF. In multivariable analysis age, gender, steroid use, serum phosphate and handgrip strength remained independently associated with SAF. CONCLUSIONS: SAF levels are elevated in RT patients and correlate with CVD risk. Besides age and male sex, our results suggest that phosphate overload, steroid use and nutritional status are important factors linking to AGEs accumulation. Public Library of Science 2018-08-01 /pmc/articles/PMC6070236/ /pubmed/30067789 http://dx.doi.org/10.1371/journal.pone.0201118 Text en © 2018 Calviño et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Calviño, Jesus
Cigarran, Secundino
Gonzalez-Tabares, Lourdes
Menendez, Nicolas
Latorre, Juan
Cillero, Sonia
Millan, Beatriz
Cobelo, Carmen
Sanjurjo-Amado, Ana
Quispe, Jansen
Garcia-Enriquez, Alba
Carrero, Juan J.
Advanced glycation end products (AGEs) estimated by skin autofluorescence are related with cardiovascular risk in renal transplant
title Advanced glycation end products (AGEs) estimated by skin autofluorescence are related with cardiovascular risk in renal transplant
title_full Advanced glycation end products (AGEs) estimated by skin autofluorescence are related with cardiovascular risk in renal transplant
title_fullStr Advanced glycation end products (AGEs) estimated by skin autofluorescence are related with cardiovascular risk in renal transplant
title_full_unstemmed Advanced glycation end products (AGEs) estimated by skin autofluorescence are related with cardiovascular risk in renal transplant
title_short Advanced glycation end products (AGEs) estimated by skin autofluorescence are related with cardiovascular risk in renal transplant
title_sort advanced glycation end products (ages) estimated by skin autofluorescence are related with cardiovascular risk in renal transplant
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6070236/
https://www.ncbi.nlm.nih.gov/pubmed/30067789
http://dx.doi.org/10.1371/journal.pone.0201118
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