Lorente Leonardo, Martín María M, Ramos Luis, Cáceres Juan J, Solé-Violán Jordi, Argueso Mónica, Jiménez Alejandro, Borreguero-León Juan M, Orbe Josune, Rodríguez José A, Páramo José A
Intensive Care Unit, Hospital Universitario de Canarias, Ofra, s/n. La Laguna, 38320, Santa Cruz de Tenerife, Spain.
Intensive Care Unit, Hospital Universitario Nuestra Señora de Candelaria, Crta del Rosario s/n, Santa Cruz de Tenerife, 38010, Spain.
BMC Neurol. 2015 Jul 11;15:111. doi: 10.1186/s12883-015-0364-7.
In the last years, circulating matrix metalloproteinases (MMP)-9 levels have been associated with functional outcome in ischemic stroke patients. However the prognostic value of circulating levels of tissue inhibitor of matrix metalloproteinases (TIMP)-1 and MMP-10 in functional outcome of ischemic stroke patients has been scarcely studied. In addition, to our knowledge, serum MMP-9, MMP-10 and TIMP-1 levels in patients with malignant middle cerebral artery infarction (MMCAI) for mortality prediction have not been studied, and these were the objectives of this study.
This was a multicenter, observational and prospective study carried out in six Spanish Intensive Care Units. We included patients with severe MMCAI defined as Glasgow Coma Scale (GCS) lower than 9. We measured circulating levels of MMP-9, MMP-10, TIMP-1, in 50 patients with severe MMCAI at diagnosis and in 50 healthy subjects. Endpoint was 30-day mortality.
Patients with severe MMCAI showed higher serum levels of MMP-9 (p = 0.001), MMP-10 (p < 0.001), and TIMP-1 (p = 0.02) than healthy subjects. Non-surviving MMCAI patients (n = 26) compared to survivor ones (n = 24) showed higher circulating levels of TIMP-1 (p < 0.001), MMP-10 (p = 0.02) and PAI-1(p = 0.02), and lower MMP-9 levels (p = 0.04). Multiple binomial logistic regression analysis showed that serum TIMP-1 levels > 239 ng/mL are associated with 30-day mortality (OR = 5.82; 95% CI = 1.37-24.73; P = 0.02) controlling for GCS and age. The area under the curve for TIMP-1 as predictor of 30-day mortality was 0.81 (95% CI = 0.67-0.91; P < 0.001). We found an association between circulating levels of TIMP-1 and MMP-10 (rho = 0.45; P = 0.001), plasminogen activator inhibitor (PAI)-1 (rho = 0.53; P < 0.001), and tumor necrosis factor (TNF)-alpha (rho = 0.70; P < 0.001).
The most relevant and new findings of our study, were that serum TIMP-1 levels in MMCAI patients were associated with mortality, and could be used as a prognostic biomarker of mortality in MMCAI patients.
在过去几年中,循环基质金属蛋白酶(MMP)-9水平与缺血性中风患者的功能预后相关。然而,基质金属蛋白酶组织抑制剂(TIMP)-1和MMP-10的循环水平在缺血性中风患者功能预后方面的预后价值鲜有研究。此外,据我们所知,恶性大脑中动脉梗死(MMCAI)患者的血清MMP-9、MMP-10和TIMP-1水平用于预测死亡率尚未得到研究,而这些正是本研究的目标。
这是一项在西班牙六个重症监护病房进行的多中心、观察性前瞻性研究。我们纳入了格拉斯哥昏迷量表(GCS)低于9分的严重MMCAI患者。我们在50例诊断为严重MMCAI的患者和50名健康受试者中测量了MMP-9、MMP-10、TIMP-1的循环水平。终点为30天死亡率。
严重MMCAI患者的血清MMP-9(p = 0.001)、MMP-10(p < 0.001)和TIMP-1(p = 0.02)水平高于健康受试者。与存活的MMCAI患者(n = 24)相比,未存活的MMCAI患者(n = 26)的TIMP-1(p < 0.001)、MMP-10(p = 0.02)和纤溶酶原激活物抑制剂(PAI)-1(p = 0.02)循环水平较高,而MMP-9水平较低(p = 0.04)。多项二项逻辑回归分析显示,在控制GCS和年龄的情况下,血清TIMP-1水平> 239 ng/mL与30天死亡率相关(OR = 5.82;95% CI = 1.37 - 24.73;P = 0.02)。TIMP-1作为30天死亡率预测指标的曲线下面积为0.81(95% CI = 0.67 - 0.91;P < 0.001)。我们发现TIMP-1的循环水平与MMP-10(rho = 0.45;P = 0.001)、纤溶酶原激活物抑制剂(PAI)-1(rho = 0.53;P < 0.001)和肿瘤坏死因子(TNF)-α(rho = 0.70;P < 0.001)之间存在关联。
我们研究中最相关的新发现是,MMCAI患者的血清TIMP-1水平与死亡率相关,并且可作为MMCAI患者死亡率的预后生物标志物。