Pretransplant dyslipidaemia influences primary graft dysfunction after lung transplantation

被引:6
作者
Cottini, Silvia R. [1 ]
Ehlers, Ulrike E. [1 ]
Pagnamenta, Alberto [2 ]
Brandi, Giovanna [1 ]
Weder, Walter [3 ]
Schuepbach, Reto A. [1 ]
Bechir, Markus [1 ,4 ]
Benden, Christian [5 ]
机构
[1] Univ Zurich Hosp, Surg Intens Care Med, Raemistr 100, CH-8091 Zurich, Switzerland
[2] Reg Hosp Mendrisio, Intens Care Unit, Dept Intens Care Med, Ente Osped Cantonale, Mendrisio, Switzerland
[3] Univ Zurich Hosp, Div Thorac Surg, CH-8091 Zurich, Switzerland
[4] Swiss Parapleg Ctr, Nottwil, Switzerland
[5] Univ Zurich Hosp, Div Pulm Med, CH-8091 Zurich, Switzerland
关键词
Lung transplantation; Primary graft dysfunction; Inflammation; Dyslipidaemia; HIGH-DENSITY-LIPOPROTEIN; ALLOGRAFT DYSFUNCTION; INTERNATIONAL-SOCIETY; HEART; CHOLESTEROL; RECIPIENTS; REGISTRY; HDL;
D O I
10.1093/icvts/ivv295
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES: Primary graft dysfunction (PGD) is a major cause of mortality within the first year following lung transplantation. Pulmonary hypertension, elevated body mass index (BMI), prolonged ischaemic time of the graft, intraoperative blood transfusions > 1000 ml and the use of cardiopulmonary bypass or extracorporeal membrane oxygenation increase the risk for PGD. We aimed to evaluate whether dyslipidaemia is an additional risk factor for the development of PGD. METHODS: We retrospectively analysed demographic and clinical data of 264 patients who received their first bilateral lung transplantation between March 2000 and October 2013 at our institution. The endpoint was PGD grade 3 at any time, defined according to the International Society for Heart and Lung Transplantation (ISHLT) criteria. Fasting lipid profiles at listing time or just before transplantation (baseline) were documented and dyslipidaemia was defined as any of the parameters being out of range. Comparisons of continuous variables between patients with PGD grade 3 and patients without were performed with the Mann-Whitney U-test, whereas proportions were compared with the chi(2) test. Continuous variables were presented as arithmetic means with standard deviation for ease of comparison, but levels of statistical significance were computed using the appropriate non-parametric statistical test. To identify PGD risk factors, a forward stepwise logistic regression model was used. RESULTS: PGD occurred in 63 recipients (24%). Pretransplant dyslipidaemia was documented in 153 recipients (58%) and was significantly more prevalent among recipients developing PGD (45 vs 108, P < 0.013). Despite various underlying pulmonary pathologies, higher triglyceride (TG) levels (1.41 +/- 0.78 vs 1.16 +/- 0.78, P < 0.012), lower high-density lipoprotein-cholesterol (HDL-C) concentrations (1.24 +/- 0.55 vs 1.57 +/- 0.71, P < 0.0005) and higher cholesterol/HDL-C values (3.80 +/- 2.02 vs 3.00 +/- 0.92, P < 0.0005) were associated with a lower incidence of PGD. Patients with PGD had significantly longer ischaemic time (350 +/- 89 vs 322 +/- 91, P = 0.017) and higher BMI (23 +/- 5 vs 21 +/- 4.4, P < 0.007). CONCLUSIONS: Dyslipidaemia seems to be an independent risk factor for PGD after lung transplantation: low circulating levels of HDL-C and hypertriglyceridaemia increase the incidence of PGD. Even if HDL-C levels are difficult to alter today, triglyceride and cholesterol levels can be addressed therapeutically and may have a positive influence on the development of PGD.
引用
收藏
页码:402 / 405
页数:4
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