Research Article

Do Antinuclear Antibodies Influence the Clinical Features of Chronic Spontaneous Urticaria?: A Retrospective Cohort Study

Table 3

Previous studies of chronic spontaneous urticaria with antinuclear antibodies positive results compared to our study.

Authors, year study designStudy populationANA methodPrevalence of positive ANAComparing between ANA-positive CSU patients and ANA-negative CSU patientsOthers
F : M ratioCountryDisease severityAssociated diseaseLaboratory characteristicsTreatment outcome

Viswanathan et al., [22]
Retrospective study
195 CSU patients2.8 : 1USAN/A29%N/AN/AN/ASignificant higher prevalence of patients refractory to antihistamines with or without the use of a LTRA
(50% vs. 30%),
Positive ANA has a significant odds ratio for identifying patients refractory to antihistamines with or without the use of a LTRA
(OR 2.3),
Calamita et al., [23]
Cross-sectional study
67 CSU patients2.2 : 1BrazilIIF using HEp-2 cells10.5%N/AN/AN/AN/ASignificant association between positive ANA and presence of anti-TPO (OR 5.94)
Magen et al., [24]
Retrospective study
-91 ANA-positive CSU patients
-478 ANA-negative CSU patients
-3131 ANA positive non-CSU patients
3.6 : 1IsraelFully automated Luminex-based system (BioPlex 2200 ANA screen, by Bio-Rad; Bio-Rad Laboratories, Hercules, CA)16%No significant difference
- initial UAS
(3.8 ), p =0.235
- prevalence of angioedema
(29.7% VS 23.8%),
Significant difference
- Sjögren’s syndrome
(3.3% vs. 0%),
- graves’ disease
(5.5% vs. 1.7%),
- Hashimoto’s thyroiditis
(23.1% vs. 14.2%),
- SLE
(4.4% vs. 0%),
- systemic sclerosis
(2.2% VS 0%), p =0.025
- overlap syndrome
(3.3% VS 0%), p =0.004
No significant difference
- rheumatoid arthritis
(2.2% VS 0.6%), p =0.182
- mixed connective tissue disease
(0% VS 0%), p = 1
Significant difference
- anti-TPO
(27.5% vs. 12.2%),
- Antithyroglobulin antibody
(20.9% vs. 10.4%),
- Basopenia
( VS 0.15 0.11), p = <0.001
- C-reactive protein
(6.4 10.3 VS 4.1 8.8), p = 0.027
No significant difference
- IgE (U/mL)
(185.5 346.6 VS 126.4 309.8), p = 0.102
Significant higher prevalence of patients resistant to four-fold standard licensed doses of antihistamines
(12.1% VS 6.1%), p =0.046
Ye et al., [25]
Prospective observational study
75 CSU patients2.1 : 1South KoreaIIF using HEp-2 cells10.7%N/AN/AN/AN/A
Campos et al., [26]
Cross-sectional case-control
- 27 CSU patient
- 22 controls (other hypersensitivities without urticaria)
2.4 : 1BrazilImmunoassay14.8%N/AN/AN/AN/A
Ertaş et al., 2020 [21]
Retrospective study
447 CSU patients2.4 : 1TurkeyIIF using HEp-2 cells23.9%Significant higher prevalence of angioedema
(70% vs. 53%),
Significant difference
- Sjögren’s syndrome
(4.7% vs. 0.6%),
- rheumatoid arthritis
(10.3% vs. 4.4%),
No significant difference
- thyroid disease
(24% vs. 18%),
- diabetes mellitus
(24% VS 18%), p = 0.128
- hypertension
(9% VS 11%), p = 0.651
- asthma
(20% VS 17%), p = 0.552
Significant difference
- anti-TPO
(27% VS 18%),
- Total IgE
(64 (21-160) vs. 110 (44-236)),
No significant difference
- ESR
(11 (5-18) Basopenia 8 (4-16)),
- CRP
(3.3 (3.0-7.5) vs. 3.3 (3.0-6.8)), p = 0.765
Significant higher prevalence of nonresponders (VAS improvement< 20% at week 12 of 300 mg/4weeks omalizumab treatment
(45% vs. 9%), p < 0.001
Our study
Prospective study
323 CSU patients5.1 : 1ThailandIIF using HEp-20-10 cells31%No significant difference
- maximal UAS7
(17 (0-42) vs. 15 (0-42)),
- prevalence of angioedema groups
(21.0% vs. 18.8%),
No significant difference
- thyroid disease
(8.0% vs. 5.4%),
- diabetes mellitus
(4.0% vs. 4.0%),
- hyperlipidemia
(2.0% vs. 4.5%),
- hypertension
(7.0% vs. 5.4%), p = 0.568
Significant difference
- ESR
(18.00 (4-84) vs. 14.00 (1-60)),
No significant difference
- anti-TPO
(20.0% vs. 14.7%),
No significant difference
- cumulative medication score
(8 (2-34) vs. 8 (2-29)),
- immunosuppressive drug/omalizumab use
(32.7% vs. 24.4%),
- time to remission
(9.6 years vs. 10.3 years)

Abbreviations: ANA: antinuclear antibodies; anti-TPO, and anti-thyroid peroxidase; CSU: chronic spontaneous urticaria; F: female; LTRA: leukotriene receptor antagonist; M: male; MCTD: mixed connective tissue disease; N/A: not available; SLE: systemic lupus erythematosus.