牙周治疗对印度不同牙周病非肥胖人群唾液内脂素生物标志物水平的影响——一项临床生化研究

Amita Coutinho, Neethu Reddy, M. Khan
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引用次数: 0

摘要

正确诊断和制定有效的牙周治疗对控制牙周疾病至关重要。诊断研究的快速进展正朝着通过测量生物标志物来识别和量化牙周病风险的方法发展。本研究探讨了非手术牙周病治疗(NSPT)对牙周病加重患者临床指标和唾液visfatin水平的影响。本干预性临床试验对60名全身健康的男性和女性受试者(年龄在20 ~ 50岁)进行研究,分为1组、20名牙周组织健康的受试者、2组、20名全身性中度牙龈炎患者和3组(20名中重度牙周炎患者(根据牙周病新分类的III期)。在基线和NSPT后6周,使用标准酶联免疫吸附试验(ELISA)技术测量未刺激唾液中的visfatin水平。血清visfatin水平以组3最高(38.22±3.38 ng/ml),其次为组2(26.66±2.24 ng/ml)和组1(25.60±2.19 ng/ml)。NSPT后,2组和3组唾液visfatin水平显著降低(p<0.001)。无论体重指数如何,正常体重和超重受试者的唾液内脂素水平在基线时几乎是不一致的,并且在NSPT后6周,两组唾液内脂素水平在统计学上显著降低(p<0.001)。目前的研究表明,唾液visfatin在牙周病的病理中起着重要的作用,可以作为其诊断/治疗的生物标志物。
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The Influence of Periodontal Treatment on Salivary Visfatin Biomarker levels in Non-obese Indian Population with Different forms of Periodontal Disease- A Clinico-Biochemical Study
The ability to correctly diagnose and institute effective periodontal therapy is essential to control periodontal diseases. Rapid advances in diagnostic research are moving towards methods whereby periodontal disease risk can be identified and quantified by measuring biomarkers. This study investigated the effect of Non-Surgical Periodontal Treatment (NSPT) on clinical indices and salivary levels of visfatin in subjects with increasing severity of the periodontal disease. This interventional clinical trial was performed on 60 systemically healthy male and female subjects (20 to 50 years) who were categorised into Group-1, Twenty subjects with healthy periodontium, Group-2, Twenty subjects with generalized moderate gingivitis, and Group-3 (20 subjects with moderate to severe periodontitis (Stage III according to the new classification of periodontal diseases). The visfatin levels were measured in unstimulated saliva by using standard EnzymeLinked Immunosorbent Assay (ELISA) technique at baseline and six weeks after NSPT. The salivary visfatin levels were highest in Group-3 (38.22±3.38 ng/ml) followed by Group - 2 (26.66±2.24 ng/ml) and Group-1 (25.60±2.19 ng/ml) at baseline. After NSPT statistically significant reduction in salivary visfatin levels (p<0.001) in Groups -2 and 3 were seen. Visfatin levels at baseline were almost equivocal in normal weight and overweight subjects, irrespective of body mass index and showed a statistically significant reduction in salivary visfatin levels in both groups six weeks after NSPT (p<0.001). The present study suggests that salivary visfatin is a strong contributor in the pathology of periodontal disease and can be used as its diagnostic/therapeutic biomarker.
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