Platelet cytochrome c oxidase activity and quantity in septic patients

被引:26
|
作者
Lorente, Leonardo [1 ]
Martin, Maria M. [4 ]
Lopez-Gallardo, Esther [5 ]
Iceta, Ruth [5 ]
Sole-Violan, Jordi [6 ]
Blanquer, Jose [7 ]
Labarta, Lorenzo [8 ]
Diaz, Cesar [10 ]
Jimenez, Alejandro [2 ]
Lafuente, Noelia [1 ]
Hernandez, Miriram [3 ]
Mendez, Froilan [4 ]
Medina, Nuria [4 ]
Ferrer-Agueero, Jose M. [6 ]
Ferreres, Jose [7 ]
LLiminana, Maria C. [9 ]
Mora, Maria L. [1 ]
Lubillo, Santiago [4 ]
Sanchez-Palacios, Manuel [10 ]
Montoya, Julio [5 ]
Ruiz-Pesini, Eduardo [5 ,11 ]
机构
[1] Hosp Univ Canarias, Intens Care Unit, San Cristobal La Laguna, Santa Cruz Tene, Spain
[2] Hosp Univ Canarias, Res Unit, San Cristobal La Laguna, Santa Cruz Tene, Spain
[3] Hosp Univ Canarias, Dept Microbiol, San Cristobal La Laguna, Santa Cruz Tene, Spain
[4] Hosp Univ Nuestra Senora Candelaria, Intens Care Unit, Santa Cruz De Tenerife, Spain
[5] Univ Zaragoza, Dept Bioquim & Biol Mol & Celular, Ctr Invest Biomed Red Enfermedad Raras, Inst Aragones Ciencias Salud, Zaragoza, Spain
[6] Hosp Univ Dr Negrin, Intens Care Unit, Las Palmas Gran Canaria, Spain
[7] Hosp Clin Univ, Intens Care Unit, Valencia, Spain
[8] Hosp San Jorge, Intens Care Unit, Huesca, Spain
[9] Hosp San Jorge, Dept Lab, Huesca, Spain
[10] Hosp Insular, Intens Care Unit, Las Palmas Gran Canaria, Spain
[11] Fdn Agencia Aragonesa Invest & Desarrollo, Zaragoza, Spain
关键词
mitochondria; oxidative phosphorylation; cytochrome c oxidase; sepsis; mortality; ELECTRON-TRANSPORT CHAIN; MITOCHONDRIAL DYSFUNCTION; GENE-EXPRESSION; NITRIC-OXIDE; SEPSIS; SHOCK; RESPONSES; LACTATE; DAMAGE; BIOGENESIS;
D O I
10.1097/CCM.0b013e31820ee20c
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Objective: The cytopathic hypoxia theory proposes that there is an impaired cellular oxygen utilization during sepsis. Respiratory complex IV, or cytochrome c oxidase, was only previously studied in muscle biopsies of 16 surviving and 12 nonsurviving septic patients. We hypothesized that higher activities and quantities of this enzyme complex could be associated with septic patient survival. The objective was to evaluate the relationship between cytochrome c oxidase activities and quantities and 6-month survival in a larger series of septic patients using a less invasive method (circulating platelets). Design: Prospective, multicenter, observational study. Setting: The study was carried out in six Spanish intensive care units. Patients: We included 96 septic patients. Interventions: We determined the cytochrome c oxidase activity per citrate synthase activity ratio and cytochrome c oxidase quantity per citrate synthase activity ratio in circulating platelets at the time of diagnosis and related them to 6-month survival. The written informed consent from the family members was obtained. Measurements and Main Results: Survivor patients (n = 54) showed higher cytochrome c oxidase activity per citrate synthase activity ratio (p = .04) and cytochrome c oxidase quantity per citrate synthase activity ratio (p = .006) than nonsurvivors (n = 42). Logistic regression analyses confirmed that the cytochrome c oxidase activity per citrate synthase activity ratio (p = .04) and cytochrome c oxidase quantity per citrate synthase activity ratio (p = .02) were independent predictors of 6-month survival. The area under the curve to predict 6-month survival was 0.62 (95% confidence interval 0.51-0.74; p = .04) for the cytochrome c oxidase activity per citrate synthase activity ratio and 0.67 (95% confidence interval 0.56-0.76; p = .003) for the cytochrome c oxidase quantity per citrate synthase activity ratio. A negative correlation was found between the cytochrome c oxidase quantity per citrate synthase activity ratio and Sepsis-Related Organ Failure Assessment score (p = .04). Conclusions: Platelet cytochrome c oxidase activity and quantity were independent predictors of 6-month survival and could be used as biomarkers of sepsis mortality. This is a rapid, easy, and less invasive protocol to assess mitochondrial function. Patients with lower cytochrome c oxidase activity and quantity could benefit from drugs that improve mitochondrial function. (Crit Care Med 2011; 39:1289-1294)
引用
收藏
页码:1289 / 1294
页数:6
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