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ANA-Specific Antibodies, ANA Patterns, Anti-ds DNA results, and Clinical Diagnosis: A Laboratory and Clinical Audit.

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Abstract Background: The diagnosis of systemic autoimmune diseases (SAID) is challenging, due to overlapping features with other non-immune disorders. Anti-nuclear antibodies (ANA) /anti-cellular antibodies are the sensitive screening tests but anti-double-stranded-deoxyribonucleic acid-antibody (anti-ds-DNA), and ANA-specific antibodies are specific for SAID. We aimed to look at ANA-specific antibodies in our patients and correlated them with ANA patterns, anti-ds-DNA, and clinical diagnosis for proper interpretation and better patient management cost-effectively. Methods: A retrospective data analysis of 641 patients was done (1st February 2019 to 31st –July-2021) who were tested for ANA-specific antibodies at the Immunology Department of Indus Hospital and Health Network. ANA and anti-ds-DNA results and clinical diagnosis were also analyzed for ANA-specific antibodies-positive patients. Descriptive data were presented in mean ±standard deviation and frequency percentages whereas inferential data were analyzed with a chi-square test for association between ANA-specific antibodies status, ANA, anti-ds-DNA, and clinical features. Results: ANA-specific antibodies test revealed positivity for at least one autoantibody in 245 (38.2%) patients. Of these, ANA was tested in 206 patients reactive for ANA-specific antibodies and found positive in 195 (95%) as compared to negative (<0.001). Speckled and homogenous were predominant ANA patterns in ANA-specific antibodies-positives (56% and 42% respectively). Multiple ANA patterns were found in 18 patients most commonly with systemic lupus erythematosus (SLE) and mixed connective tissue disorder (MCTD). Anti-SSA were the most common ANA-specific antibodies (50%) and was mostly found in sera with speckled (61/97) and homogenous (38/97) patterns and associated mostly with SLE (48%) and Sjogren’s syndrome (86%). Among ANA-negative patients, anti-SSA were the most common antibodies (n=5). Anti-ds-DNA was found in 66% of SLE patients along with another ANA-specific antibody. Conclusions: This study showed that testing for ANA-specific antibodies cannot be gated on ANA patterns. Also, there is a redundancy of these antibodies with various clinical diagnoses. Moreover, they are useful in making a diagnosis in ANA-negative patients as well with clinical suspicion.
Title: ANA-Specific Antibodies, ANA Patterns, Anti-ds DNA results, and Clinical Diagnosis: A Laboratory and Clinical Audit.
Description:
Abstract Background: The diagnosis of systemic autoimmune diseases (SAID) is challenging, due to overlapping features with other non-immune disorders.
Anti-nuclear antibodies (ANA) /anti-cellular antibodies are the sensitive screening tests but anti-double-stranded-deoxyribonucleic acid-antibody (anti-ds-DNA), and ANA-specific antibodies are specific for SAID.
We aimed to look at ANA-specific antibodies in our patients and correlated them with ANA patterns, anti-ds-DNA, and clinical diagnosis for proper interpretation and better patient management cost-effectively.
Methods: A retrospective data analysis of 641 patients was done (1st February 2019 to 31st –July-2021) who were tested for ANA-specific antibodies at the Immunology Department of Indus Hospital and Health Network.
ANA and anti-ds-DNA results and clinical diagnosis were also analyzed for ANA-specific antibodies-positive patients.
Descriptive data were presented in mean ±standard deviation and frequency percentages whereas inferential data were analyzed with a chi-square test for association between ANA-specific antibodies status, ANA, anti-ds-DNA, and clinical features.
Results: ANA-specific antibodies test revealed positivity for at least one autoantibody in 245 (38.
2%) patients.
Of these, ANA was tested in 206 patients reactive for ANA-specific antibodies and found positive in 195 (95%) as compared to negative (<0.
001).
Speckled and homogenous were predominant ANA patterns in ANA-specific antibodies-positives (56% and 42% respectively).
Multiple ANA patterns were found in 18 patients most commonly with systemic lupus erythematosus (SLE) and mixed connective tissue disorder (MCTD).
Anti-SSA were the most common ANA-specific antibodies (50%) and was mostly found in sera with speckled (61/97) and homogenous (38/97) patterns and associated mostly with SLE (48%) and Sjogren’s syndrome (86%).
Among ANA-negative patients, anti-SSA were the most common antibodies (n=5).
Anti-ds-DNA was found in 66% of SLE patients along with another ANA-specific antibody.
Conclusions: This study showed that testing for ANA-specific antibodies cannot be gated on ANA patterns.
Also, there is a redundancy of these antibodies with various clinical diagnoses.
Moreover, they are useful in making a diagnosis in ANA-negative patients as well with clinical suspicion.

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