Plasma malondialdehyde and risk of new-onset diabetes after transplantation in renal transplant recipients: A prospective cohort study

Research output: Contribution to journalArticleResearchpeer review

Authors

  • Manuela Yepes-Calderón
  • Camilo G. Sotomayor
  • António W. Gomes-Neto
  • Rijk O.B. Gans
  • Stefan P. Berger
  • G. Rimbach
  • Tuba Esatbeyoglu
  • Ramón Rodrigo
  • Johanna M. Geleijnse
  • Gerjan J. Navis
  • Stephan J.L. Bakker

External Research Organisations

  • University Medical Center Groningen (UMCG)
  • University of Chile
  • Wageningen University and Research
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Details

Original languageEnglish
Article number453
JournalJournal of Clinical Medicine
Volume8
Issue number4
Early online date4 Apr 2019
Publication statusPublished - Apr 2019

Abstract

New-onset diabetes after transplantation (NODAT) is a frequent complication in renal transplant recipients (RTR). Although oxidative stress has been associated with diabetes mellitus, data regarding NODAT are limited. We aimed to prospectively investigate the long-term association between the oxidative stress biomarker malondialdehyde (measured by high-performance liquid chromatography) and NODAT in an extensively phenotyped cohort of non-diabetic RTR with a functioning graft ≥1 year. We included 516 RTR (51 ± 13 years-old, 57% male). Median plasma malondialdehyde (MDA) was 2.55 (IQR, 1.92-3.66) µmol/L. During a median follow-up of 5.3 (IQR, 4.6-6.0) years, 56 (11%) RTR developed NODAT. In Cox proportional-hazards regression analyses, MDA was inversely associated with NODAT, independent of immunosuppressive therapy, transplant-specific covariates, lifestyle, inflammation, and metabolism parameters (HR, 0.55; 95% CI, 0.36-0.83 per 1-SD increase; p < 0.01). Dietary antioxidants intake (e.g., vitamin E, α-lipoic acid, and linoleic acid) were effect-modifiers of the association between MDA and NODAT, with particularly strong inverse associations within the subgroup of RTR with relatively higher dietary antioxidants intake. In conclusion, plasma MDA concentration is inversely and independently associated with long-term risk of NODAT in RTR. Our findings support a potential underrecognized role of oxidative stress in post-transplantation glucose homeostasis.

Keywords

    Malondialdehyde, New-onset diabetes, Oxidative stress, Renal transplantation

ASJC Scopus subject areas

Sustainable Development Goals

Cite this

Plasma malondialdehyde and risk of new-onset diabetes after transplantation in renal transplant recipients: A prospective cohort study. / Yepes-Calderón, Manuela; Sotomayor, Camilo G.; Gomes-Neto, António W. et al.
In: Journal of Clinical Medicine, Vol. 8, No. 4, 453, 04.2019.

Research output: Contribution to journalArticleResearchpeer review

Yepes-Calderón, M, Sotomayor, CG, Gomes-Neto, AW, Gans, ROB, Berger, SP, Rimbach, G, Esatbeyoglu, T, Rodrigo, R, Geleijnse , JM, Navis, GJ & Bakker, SJL 2019, 'Plasma malondialdehyde and risk of new-onset diabetes after transplantation in renal transplant recipients: A prospective cohort study', Journal of Clinical Medicine, vol. 8, no. 4, 453. https://doi.org/10.3390/jcm8040453, https://doi.org/10.15488/10958
Yepes-Calderón, M., Sotomayor, C. G., Gomes-Neto, A. W., Gans, R. O. B., Berger, S. P., Rimbach, G., Esatbeyoglu, T., Rodrigo, R., Geleijnse , J. M., Navis, G. J., & Bakker, S. J. L. (2019). Plasma malondialdehyde and risk of new-onset diabetes after transplantation in renal transplant recipients: A prospective cohort study. Journal of Clinical Medicine, 8(4), Article 453. https://doi.org/10.3390/jcm8040453, https://doi.org/10.15488/10958
Yepes-Calderón M, Sotomayor CG, Gomes-Neto AW, Gans ROB, Berger SP, Rimbach G et al. Plasma malondialdehyde and risk of new-onset diabetes after transplantation in renal transplant recipients: A prospective cohort study. Journal of Clinical Medicine. 2019 Apr;8(4):453. Epub 2019 Apr 4. doi: 10.3390/jcm8040453, 10.15488/10958
Yepes-Calderón, Manuela ; Sotomayor, Camilo G. ; Gomes-Neto, António W. et al. / Plasma malondialdehyde and risk of new-onset diabetes after transplantation in renal transplant recipients: A prospective cohort study. In: Journal of Clinical Medicine. 2019 ; Vol. 8, No. 4.
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title = "Plasma malondialdehyde and risk of new-onset diabetes after transplantation in renal transplant recipients: A prospective cohort study",
abstract = "New-onset diabetes after transplantation (NODAT) is a frequent complication in renal transplant recipients (RTR). Although oxidative stress has been associated with diabetes mellitus, data regarding NODAT are limited. We aimed to prospectively investigate the long-term association between the oxidative stress biomarker malondialdehyde (measured by high-performance liquid chromatography) and NODAT in an extensively phenotyped cohort of non-diabetic RTR with a functioning graft ≥1 year. We included 516 RTR (51 ± 13 years-old, 57% male). Median plasma malondialdehyde (MDA) was 2.55 (IQR, 1.92-3.66) µmol/L. During a median follow-up of 5.3 (IQR, 4.6-6.0) years, 56 (11%) RTR developed NODAT. In Cox proportional-hazards regression analyses, MDA was inversely associated with NODAT, independent of immunosuppressive therapy, transplant-specific covariates, lifestyle, inflammation, and metabolism parameters (HR, 0.55; 95% CI, 0.36-0.83 per 1-SD increase; p < 0.01). Dietary antioxidants intake (e.g., vitamin E, α-lipoic acid, and linoleic acid) were effect-modifiers of the association between MDA and NODAT, with particularly strong inverse associations within the subgroup of RTR with relatively higher dietary antioxidants intake. In conclusion, plasma MDA concentration is inversely and independently associated with long-term risk of NODAT in RTR. Our findings support a potential underrecognized role of oxidative stress in post-transplantation glucose homeostasis. ",
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author = "Manuela Yepes-Calder{\'o}n and Sotomayor, {Camilo G.} and Gomes-Neto, {Ant{\'o}nio W.} and Gans, {Rijk O.B.} and Berger, {Stefan P.} and G. Rimbach and Tuba Esatbeyoglu and Ram{\'o}n Rodrigo and Geleijnse, {Johanna M.} and Navis, {Gerjan J.} and Bakker, {Stephan J.L.}",
note = "Funding: This study was based on the TransplantLines Food and Nutrition Biobank and Cohort Study (TxL-FN), which was funded by the Top Institute Food and Nutrition of the Netherlands (grant A-1003). The study is registered at clinicaltrials.gov under number NCT02811835.",
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T1 - Plasma malondialdehyde and risk of new-onset diabetes after transplantation in renal transplant recipients: A prospective cohort study

AU - Yepes-Calderón, Manuela

AU - Sotomayor, Camilo G.

AU - Gomes-Neto, António W.

AU - Gans, Rijk O.B.

AU - Berger, Stefan P.

AU - Rimbach, G.

AU - Esatbeyoglu, Tuba

AU - Rodrigo, Ramón

AU - Geleijnse , Johanna M.

AU - Navis, Gerjan J.

AU - Bakker, Stephan J.L.

N1 - Funding: This study was based on the TransplantLines Food and Nutrition Biobank and Cohort Study (TxL-FN), which was funded by the Top Institute Food and Nutrition of the Netherlands (grant A-1003). The study is registered at clinicaltrials.gov under number NCT02811835.

PY - 2019/4

Y1 - 2019/4

N2 - New-onset diabetes after transplantation (NODAT) is a frequent complication in renal transplant recipients (RTR). Although oxidative stress has been associated with diabetes mellitus, data regarding NODAT are limited. We aimed to prospectively investigate the long-term association between the oxidative stress biomarker malondialdehyde (measured by high-performance liquid chromatography) and NODAT in an extensively phenotyped cohort of non-diabetic RTR with a functioning graft ≥1 year. We included 516 RTR (51 ± 13 years-old, 57% male). Median plasma malondialdehyde (MDA) was 2.55 (IQR, 1.92-3.66) µmol/L. During a median follow-up of 5.3 (IQR, 4.6-6.0) years, 56 (11%) RTR developed NODAT. In Cox proportional-hazards regression analyses, MDA was inversely associated with NODAT, independent of immunosuppressive therapy, transplant-specific covariates, lifestyle, inflammation, and metabolism parameters (HR, 0.55; 95% CI, 0.36-0.83 per 1-SD increase; p < 0.01). Dietary antioxidants intake (e.g., vitamin E, α-lipoic acid, and linoleic acid) were effect-modifiers of the association between MDA and NODAT, with particularly strong inverse associations within the subgroup of RTR with relatively higher dietary antioxidants intake. In conclusion, plasma MDA concentration is inversely and independently associated with long-term risk of NODAT in RTR. Our findings support a potential underrecognized role of oxidative stress in post-transplantation glucose homeostasis.

AB - New-onset diabetes after transplantation (NODAT) is a frequent complication in renal transplant recipients (RTR). Although oxidative stress has been associated with diabetes mellitus, data regarding NODAT are limited. We aimed to prospectively investigate the long-term association between the oxidative stress biomarker malondialdehyde (measured by high-performance liquid chromatography) and NODAT in an extensively phenotyped cohort of non-diabetic RTR with a functioning graft ≥1 year. We included 516 RTR (51 ± 13 years-old, 57% male). Median plasma malondialdehyde (MDA) was 2.55 (IQR, 1.92-3.66) µmol/L. During a median follow-up of 5.3 (IQR, 4.6-6.0) years, 56 (11%) RTR developed NODAT. In Cox proportional-hazards regression analyses, MDA was inversely associated with NODAT, independent of immunosuppressive therapy, transplant-specific covariates, lifestyle, inflammation, and metabolism parameters (HR, 0.55; 95% CI, 0.36-0.83 per 1-SD increase; p < 0.01). Dietary antioxidants intake (e.g., vitamin E, α-lipoic acid, and linoleic acid) were effect-modifiers of the association between MDA and NODAT, with particularly strong inverse associations within the subgroup of RTR with relatively higher dietary antioxidants intake. In conclusion, plasma MDA concentration is inversely and independently associated with long-term risk of NODAT in RTR. Our findings support a potential underrecognized role of oxidative stress in post-transplantation glucose homeostasis.

KW - Malondialdehyde

KW - New-onset diabetes

KW - Oxidative stress

KW - Renal transplantation

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U2 - 10.3390/jcm8040453

DO - 10.3390/jcm8040453

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C2 - 30987358

VL - 8

JO - Journal of Clinical Medicine

JF - Journal of Clinical Medicine

SN - 2077-0383

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