Gupta Shalini R, Xess Immaculata, Singh Gagandeep, Sharma Alpana, Gupta Nidhi, Mani Kalaivani, Sharma Sheetal
Oral Medicine & Radiology Centre for Dental Education Research All India Institute of Medical Sciences New Delhi India.
Microbiology AIIMS N Delhi, India.
J Oral Biol Craniofac Res. 2021 Apr-Jun;11(2):354-360. doi: 10.1016/j.jobcr.2021.03.006. Epub 2021 Mar 19.
To determine the association of phenotypes, virulence factors, antifungal sensitivity and clinical response to Fluconazole in Oral leukoplakia (OL).
Sterile swabs were obtained from oral lesions in immunocompetent subjects [30 Homogenous (HOL), 31 Non- Homogenous (NHOL] and normal buccal mucosa in 30 age and sex-matched healthy controls (C). phenotypes, virulence factors (Secreted Aspartyl Proteinase (SAP), Phospholipase (PL), Biofilm formation (BF) and antifungal sensitivity were determined. Clinical features (Size, Erythema, thickness, oral burning sensation (VAS scores) before and after Fluconazole therapy in OL were recorded by two calibrated observers.
was associated with OL (p < 0.01). was the most common phenotype sensitive to Fluconazole. SAP, PL and BF activity was significantly high in NHOL. Strong positive correlation was seen between SAP, and PL activity and pre-treatment VAS scores in NHOL. There was significant reduction in VAS scores, size of lesion [HOL (p < 0.001) NHOL (p < 0.05)], erythematous areas (67.8%) in NHOL and thickness of lesions (42.6%) in both types OL after Fluconazole therapy with substantial inter-observer agreement. Non (NAC) species had similar virulence profiles but resistant to Fluconazole and showed minimal clinical improvement.
Virulence activity of in OL increases severity of lesions. Fluconazole is effective against virulent , causes clinical improvement and down-staging from high -risk NHOL to low-risk HOL which can reduce risk of malignant transformation. Detection of highly virulent NAC infection and antifungal sensitivity is recommended in OL recalcitrant to Fluconazole therapy.
确定口腔白斑(OL)的表型、毒力因子、抗真菌敏感性与氟康唑临床反应之间的关联。
从免疫功能正常的受试者的口腔病变处(30例均质型(HOL)、31例非均质型(NHOL))以及30例年龄和性别匹配的健康对照者(C)的正常颊黏膜处获取无菌拭子。测定表型、毒力因子(分泌天冬氨酸蛋白酶(SAP)、磷脂酶(PL)、生物膜形成(BF))和抗真菌敏感性。由两名经过校准的观察者记录OL患者在氟康唑治疗前后的临床特征(大小、红斑、厚度、口腔烧灼感(视觉模拟评分(VAS)))。
[此处原文缺失具体结果内容]与OL相关(p<0.01)。[此处原文缺失具体结果内容]是对氟康唑最敏感的常见表型。NHOL中SAP、PL和BF活性显著较高。NHOL中SAP和PL活性与治疗前VAS评分之间存在强正相关。氟康唑治疗后,VAS评分、病变大小[HOL(p<0.001),NHOL(p<0.05)]、NHOL中的红斑面积(67.8%)以及两种类型OL中的病变厚度(42.6%)均显著降低,观察者间一致性良好。非[此处原文缺失具体菌种名称](NAC)菌种具有相似的毒力特征,但对氟康唑耐药,临床改善极小。
OL中[此处原文缺失具体菌种名称]的毒力活性增加病变严重程度。氟康唑对有毒力的[此处原文缺失具体菌种名称]有效,可导致临床改善,并使从高风险的NHOL降级为低风险的HOL,从而降低恶变风险。对于氟康唑治疗无效的OL,建议检测高毒力NAC感染和抗真菌敏感性。