To Estimate and Compare the Level of Serum Immunoglobulin A in Patients of Oral Submucous Fibrosis, Leukoplakia, and Control Group

Author:

Shele Sweta Prakash1,Bhagwat Pooja P2,Yadav Renu3,Deshmukh Sonali2,Ghaisas Shraddha4,Samanta Anwesha5

Affiliation:

1. Department of Oral Pathology and Microbiology, Rural Dental College, PIMS, Loni, Maharashtra, India

2. Department of Oral Pathology and Microbiology, VYWS Dental College, Amravati, Maharashtra, India

3. Assistant Professor, Oral Pathology and Microbiology, MGV’s KBH Dental College and Hospital, Nashik, Maharashtra, India

4. Department of Oral Pathology and Microbiology, MGM Dental College and Hospital, Kamothe, Navi Mumbai, Maharashtra, India

5. Department of Oral Medicine and Radiology, Rural Dental College, Loni, Ahmednagar, Maharashtra, India

Abstract

ABSTRACT Aim: To estimate and compare the level of serum immunoglobulin A in patients of oral submucous fibrosis (OSMF), leukoplakia, and control group. Introduction: OSMF is a well-recognized potentially malignant condition in the oral cavity, and a transformation rate as high as 7.6% over a period of 10 years has been reported from India. Leukoplakia has evolved as a clinico-pathologic concept over many years, with the current clinical designation being accepted worldwide. Materials and Methods: Quantia IgA is a turbidometric immunoassay for the detection of IgA in human serum and is based on the principle of agglutination reaction. The test specimen is mixed with the activation buffer (R1) and then with antihuman IgA reagent (R2) and allowed to react. For the estimation of serum IgA, 500 μl of Quantia IgA activation buffer R1 is taken in a clean test tube. Serum sample is diluted in the ratio of 1:5 with normal saline. Ten microliters of diluted serum sample are added to R1. After incubation for 10 min, 50 μl of R2 is added, which is Quantia IgA antihuman IgA reagent to the sample, and the reading is recorded at wavelength 340 nm at 37°C. The level of IgA will be estimated by a semi-automatic biochemical analyzer machine and then data analysis will be done. Results: The immunologic alterations observed by us in OSMF and leukoplakia are almost similar or nearer to the alterations observed in oral cancer, so it is reasonable to assume that OSMF and leukoplakia can be an intermediate stage in the transformation process of a normal cell to oral malignancy. Conclusion: Prevention and early detection is the best way to reduce the incidence and mortality of premalignant disorders and oral cancer. There are many ways and methods of early detection of premalignant disorders and oral cancer, and the immunological method is one of them.

Publisher

Medknow

Reference12 articles.

1. Biochemical changes in OSMF;Bansal;J Adv Med Dent Sci,2013

2. Oral submucous fibrosis:A review article on etiopathogenesis;Tak;Kathmandu Univ Med J (KUMJ),2014

3. Oral submucous fibrosis:An update;Wollina;Clin Cosmet Investig Dermatol,2015

4. Estimation and comparison of salivary immunoglobulin A levels in tobacco chewers, tobacco smokers and normal subjects;Doni;Oral Health Dent Manag,2013

5. Research Achievements of Oral Submucous Fibrosis:Progress and Prospect;Xu;Biomed Res Int,2021

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