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Research Article | Volume 18 Issue 2 (Apr-Jun, 2025) | Pages 130 - 136
Seroprevalence and Pattern Interpretation of Anti-Nuclear Antibodies in Connective Tissue Disorders Using Indirect Immunofluorescence
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 ,
1
Assistant Professor, Department of Microbiology, Government Sivagangai Medical College Sivagangai 630561, Tamil Nadu, India
2
Department of Paediatrics, Government Hospital, Melur 625106, Madurai, Tamil nadu, India
3
Assistant Professor, Department of Microbiology, Government Dharmapuri Medical College Dharmapuri-636701, Tamilnadu, India
Under a Creative Commons license
Open Access
Received
June 5, 2025
Revised
June 10, 2025
Accepted
June 16, 2025
Published
June 18, 2025
Abstract

Background:Connective tissue disorders (CTDs) are a group of autoimmune diseases characterized by the presence of circulating antinuclear antibodies (ANA), which serve as critical biomarkers for early diagnosis. Indirect immunofluorescence (IIF) on HEp-2 cells remains the gold standard for ANA detection and enables interpretation of distinct fluorescence patterns that are often disease-specific.

Objective:To evaluate the seroprevalence of ANA and to analyze the distribution and clinical significance of fluorescence patterns observed by IIF in patients clinically suspected of CTDs.

Methods:A cross-sectional study was conducted over a five-month period involving 90 patients with clinical suspicion of CTDs. Serum samples were tested for ANA using a commercial HEp-2 IIF assay at a screening dilution of 1:80. Positive samples were further categorized based on fluorescence patterns, and the results were analyzed in relation to age, gender, and probable clinical diagnosis.

Results:Of the 90 samples tested, 59 (65.6%) were positive for ANA. ANA positivity was significantly higher in females (73%) compared to males (48%) (p < 0.05). The most common fluorescence pattern was speckled (35.6%), followed by homogenous (27.1%), nucleolar (15.2%), peripheral (10.1%), centromere (6.8%), and cytoplasmic (5.1%). The homogenous pattern was primarily associated with suspected systemic lupus erythematosus, while nucleolar and centromere patterns were linked with systemic sclerosis. ANA positivity was highest in the 31–50 years age group.

Conclusion:IIF remains a highly sensitive and informative method for ANA detection in suspected CTD patients. The interpretation of fluorescence patterns provides valuable diagnostic clues and aids in the clinical stratification of autoimmune diseases. These findings support the continued use of IIF as a frontline serological tool in the diagnostic workup of CTDs.

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