CARBOXYHEMOGLOBIN, SMOKING EXPOSURE, AND MORTALITY IN KIDNEY TRANSPLANT RECIPIENTS

 

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CARBOXYHEMOGLOBIN, SMOKING EXPOSURE, AND MORTALITY IN KIDNEY TRANSPLANT RECIPIENTS

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Sovia
Salamah
Sovia Salamah s.salamah@umcg.nl University Medical Center Groningen Internal Medicine Groningen Netherlands *
Antonio W.G. Neto a.w.gomes.neto@umcg.nl University Medical Center Groningen Internal Medicine Groningen Netherlands -
Firas Farisi Alkaff f.f.alkaff@umcg.nl University Medical Center Groningen Internal Medicine Groningen Netherlands - Universitas Airlangga Anatomy, Histology, and Pharmacology Surabaya Indonesia
Jip Jonker j.jonker02@umcg.nl University Medical Center Groningen Internal Medicine Groningen Netherlands -
Jenny E. Kootstra-Ros j.e.kootstra@umcg.nl University Medical Center Groningen Laboratory Medicine Groningen Netherlands -
Daan J. Touw d.j.touw@umcg.nl University of Groningen Pharmaceutical Analysis Groningen Netherlands -
Eva Corpelijn e.corpeleijn@umcg.nl University Medical Center Groningen Epidemiology Groningen Netherlands -
Transplantlines Investigators datarequest.transplantlines@umcg.nl University Medical Center Groningen Internal Medicine Groningen Netherlands -
Casper F.M. Franssen c.f.m.franssen@umcg.nl University Medical Center Groningen Internal Medicine Groningen Netherlands -
Stephan J.L. Bakker s.j.l.bakker@umcg.nl University Medical Center Groningen Internal Medicine Groningen Netherlands -
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Smoking is a significant risk factor for increased mortality in kidney transplant recipients (KTR). While KDIGO guidelines recommend annual tobacco use screening for KTR, self-reported smoking status is often unreliable, and urinary cotinine testing, considered the gold standard, is costly. Carboxyhemoglobin (COHb) has emerged as a reliable and cost-effective biomarker for identifying active smokers in KTR, with a cutoff value of 1.5% to classify active smoking. This study aims to explore the association between COHb levels, smoking exposure, and mortality in this population.

Plasma COHb was obtained from venous blood samples and measured using hemoxymetry as part of blood gas analysis. Smoking status was assessed through a questionnaire. Cox regression analyses were conducted to evaluate the association between COHb levels and mortality.

Among 1328 KTR (mean age 57 ± 14 years, 49% female, median time post-transplant 12 [IQR 12-85] months), the median COHb level was 0.93% [IQR 0.83-1.23%]. The prevalence of active smokers and history of delayed graft function occurring directly after transplantation were higher following the increasing COHb level (p < 0.001 and p=0.025, respectively). Triglyceride, C-reactive protein, and urinary albumin excretion were significantly higher according to increasing COHb level (p < 0.001, p < 0.001, and p = 0.026, respectively). Estimated glomerular filtration rate was not associated with COHb levels. During a median follow-up of 4 years, 189 (14.2%) patients died. Higher COHb levels were independently associated with higher mortality risk (hazard ratio [95% Confidence Interval (CI)] per standard deviation increase = 1.23 [1.11-1.37], p < 0.001). This association remained independent of adjustment for potential confounders, even including smoking status assessed by questionnaire (HR= 1.34 [95% CI 1.19-1.51], p < 0.001, model 4, Table 1). Kaplan-Meier curve analysis showed that patients survival probability was significantly lower among individuals with higher COHb levels (Figure 1).



COHb, which previously recognized as a reliable biomarker for detecting active smokers and more accessible than urinary cotinine, was found to be independently associated with an increased risk of mortality in KTR. Regular evaluation of COHb levels in clinical practice can improve physicians' awareness of patients' smoking status, enabling timely interventions to reduce mortality risk. This abstract was previously submitted and published in the 62nd European Renal Association (ERA) Congress abstract book (doi.org/10.1093/ndt/gfaf116.0859).

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