Deparment of Medical Laboratory Technicianship, Vocational School of Health Related Professions, Marmara University, İstanbul, Turkey.
Sleep Disorders Unit, Chest Diseases Clinics, Süreyyapaşa Research and Education Hospital, İstanbul, Turkey.
Balkan Med J. 2013 Mar;30(1):8-12. doi: 10.5152/balkanmedj.2012.068. Epub 2012 Oct 8.
Obstructive sleep apnea syndrome (OSAS) is associated with increased cardiovascular morbidity and mortality. We aimed to investigate the matrix metalloproteinase-9 (MMP-9) level and MMP-9 gene polymorphism in sleep apnea patients with or without cardiovascular disease.
Case-control study.
Two hundred nine patients [Mean age (±SD), 47 (±12) yrs; M/F, 170/39] diagnosed with sleep-disordered breathing were included in the study. Serum MMP-9 level was performed using enzyme-linked immunosorbant assay (ELISA) and MMP-9 gene polymorphism with polymerase chain reaction-restriction fragment length polymorphism. We divided the patient group into two subgroups: (1) patients with confirmed cardiovascular disease, i.e. CV-P Group and (2) patients without cardiovascular disease, CV-N Group. We compared all parameters between the two groups.
There were 56 OSAS patients with cardiovascular disorder (CV-positive group) and 153 OSAS patients without cardiovascular disorder (CV-negative group). CC, CT and TT genotype distributions between groups were similar [31 (55%), 25 (45%), 0 (0%) vs 88 (57%), 61 (40%), 4 (3%); respectively, p>0.05]. MMP-9 level was significantly higher in CV-P patients (442.7±139.3 pg/mL) than in CV-N patients (364.4±165.0 pg/mL; p=0.0018).
Our results showed that the presence of MMP-9 polymorphism was not associated with cardiovascular disease. MMP-9 level was higher in OSAS patients with cardiovascular disorders than without cardiovascular disorders. Finally, MMP-9 genotype was not associated with serum MMP-9 levels.
阻塞性睡眠呼吸暂停综合征(OSAS)与心血管发病率和死亡率的增加有关。我们旨在研究伴有或不伴有心血管疾病的睡眠呼吸暂停患者中基质金属蛋白酶-9(MMP-9)水平和 MMP-9 基因多态性。
病例对照研究。
209 例(平均年龄(±标准差),47(±12)岁;M/F,170/39)诊断为睡眠呼吸障碍的患者纳入本研究。采用酶联免疫吸附试验(ELISA)检测血清 MMP-9 水平,采用聚合酶链反应-限制性片段长度多态性检测 MMP-9 基因多态性。我们将患者分为两组:(1)有明确心血管疾病的患者,即 CV-P 组,(2)无心血管疾病的患者,即 CV-N 组。我们比较了两组之间的所有参数。
56 例 OSAS 患者合并心血管疾病(CV 阳性组),153 例 OSAS 患者无心血管疾病(CV 阴性组)。两组间 CC、CT 和 TT 基因型分布相似[31(55%)、25(45%)、0(0%)与 88(57%)、61(40%)、4(3%);分别,p>0.05]。CV-P 患者 MMP-9 水平明显高于 CV-N 患者(442.7±139.3 pg/ml 比 364.4±165.0 pg/ml;p=0.0018)。
我们的结果表明,MMP-9 多态性的存在与心血管疾病无关。伴有心血管疾病的 OSAS 患者的 MMP-9 水平高于不伴有心血管疾病的患者。最后,MMP-9 基因型与血清 MMP-9 水平无关。