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Impact of pretreatment with carnitine and tadalafil on contrast-induced nephropathy in CKD patients

Objective: The present study assesses whether phosphodiesterase type 5 (PDE-5) inhibitor or carnitine exert nephroprotective effects against clinical contrast-induced nephropathy (CIN). Materials and Methods: The present study consisted of three groups of CKD patients. The first group was control gr...

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Autores principales: Armaly, Zaher, Artol, Suheil, Jabbour, Adel R., Saffouri, Amer, Habashi, Nayef, Abd Elkadir, Amir, Ghattas, Naser, Farah, Raymond, Kinaneh, Safa, Nseir, William
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6913644/
https://www.ncbi.nlm.nih.gov/pubmed/31797710
http://dx.doi.org/10.1080/0886022X.2019.1669459
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author Armaly, Zaher
Artol, Suheil
Jabbour, Adel R.
Saffouri, Amer
Habashi, Nayef
Abd Elkadir, Amir
Ghattas, Naser
Farah, Raymond
Kinaneh, Safa
Nseir, William
author_facet Armaly, Zaher
Artol, Suheil
Jabbour, Adel R.
Saffouri, Amer
Habashi, Nayef
Abd Elkadir, Amir
Ghattas, Naser
Farah, Raymond
Kinaneh, Safa
Nseir, William
author_sort Armaly, Zaher
collection PubMed
description Objective: The present study assesses whether phosphodiesterase type 5 (PDE-5) inhibitor or carnitine exert nephroprotective effects against clinical contrast-induced nephropathy (CIN). Materials and Methods: The present study consisted of three groups of CKD patients. The first group was control group, who were treated with N-acetyl-L-cysteine 1 day before and on the day of radiocontrast administration. The second one was carnitine group, where the patients were infused with carnitine over 10 min 2 h prior to the radiocontrast administration and 24 h post CT. The third one was PDE-5 inhibitor group, where patients were given tadalafil 2 h prior to the administration of the radiocontrast and in the subsequent day. Urine and blood samples were collected before and at the following time sequence: 2, 6, 12, 24, 48, and 120 h after the contrast administration, for creatinine and NGAL determination. Results: Pretreated with N-acetyl-L-cysteine prior to administration of contrast media (CM) to CKD patients caused a significant increase in urinary but not of plasma neutrophil gelatinase-associated lipocalin (NGAL) and serum creatinine (SCr). In contrast, pretreatment with carnitine prevented the increase in urinary NGAL and reduced SCr below basal levels. Similarly, tadalafil administration diminished the elevation of CM-induced urinary NGAL. Conclusions: These results indicate that carnitine and PDE-5 inhibitors may comprise potential therapeutic maneuvers for CIN.
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spelling pubmed-69136442019-12-18 Impact of pretreatment with carnitine and tadalafil on contrast-induced nephropathy in CKD patients Armaly, Zaher Artol, Suheil Jabbour, Adel R. Saffouri, Amer Habashi, Nayef Abd Elkadir, Amir Ghattas, Naser Farah, Raymond Kinaneh, Safa Nseir, William Ren Fail Clinical Study Objective: The present study assesses whether phosphodiesterase type 5 (PDE-5) inhibitor or carnitine exert nephroprotective effects against clinical contrast-induced nephropathy (CIN). Materials and Methods: The present study consisted of three groups of CKD patients. The first group was control group, who were treated with N-acetyl-L-cysteine 1 day before and on the day of radiocontrast administration. The second one was carnitine group, where the patients were infused with carnitine over 10 min 2 h prior to the radiocontrast administration and 24 h post CT. The third one was PDE-5 inhibitor group, where patients were given tadalafil 2 h prior to the administration of the radiocontrast and in the subsequent day. Urine and blood samples were collected before and at the following time sequence: 2, 6, 12, 24, 48, and 120 h after the contrast administration, for creatinine and NGAL determination. Results: Pretreated with N-acetyl-L-cysteine prior to administration of contrast media (CM) to CKD patients caused a significant increase in urinary but not of plasma neutrophil gelatinase-associated lipocalin (NGAL) and serum creatinine (SCr). In contrast, pretreatment with carnitine prevented the increase in urinary NGAL and reduced SCr below basal levels. Similarly, tadalafil administration diminished the elevation of CM-induced urinary NGAL. Conclusions: These results indicate that carnitine and PDE-5 inhibitors may comprise potential therapeutic maneuvers for CIN. Taylor & Francis 2019-12-04 /pmc/articles/PMC6913644/ /pubmed/31797710 http://dx.doi.org/10.1080/0886022X.2019.1669459 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 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 work is properly cited.
spellingShingle Clinical Study
Armaly, Zaher
Artol, Suheil
Jabbour, Adel R.
Saffouri, Amer
Habashi, Nayef
Abd Elkadir, Amir
Ghattas, Naser
Farah, Raymond
Kinaneh, Safa
Nseir, William
Impact of pretreatment with carnitine and tadalafil on contrast-induced nephropathy in CKD patients
title Impact of pretreatment with carnitine and tadalafil on contrast-induced nephropathy in CKD patients
title_full Impact of pretreatment with carnitine and tadalafil on contrast-induced nephropathy in CKD patients
title_fullStr Impact of pretreatment with carnitine and tadalafil on contrast-induced nephropathy in CKD patients
title_full_unstemmed Impact of pretreatment with carnitine and tadalafil on contrast-induced nephropathy in CKD patients
title_short Impact of pretreatment with carnitine and tadalafil on contrast-induced nephropathy in CKD patients
title_sort impact of pretreatment with carnitine and tadalafil on contrast-induced nephropathy in ckd patients
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6913644/
https://www.ncbi.nlm.nih.gov/pubmed/31797710
http://dx.doi.org/10.1080/0886022X.2019.1669459
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