Systemic vasculitis with latent tuberculosis infection and associated factors: a cross-sectional multicenter study.

Publication date: Jan 21, 2025

Systemic vasculitis patients are at a higher risk of developing latent tuberculosis infection (LTBI). However, there is currently no literature elucidating the positivity rate and risk factors for LTBI in systemic vasculitis patients. Our study is a multi-center, cross-sectional study that enrolled systemic vasculitis patients from 13 comprehensive hospitals in China. T-SPOT. TB as the screening method for LTBI, the study investigated the positivity rate of LTBI in systemic vasculitis patients and the factors associated with T-SPOT. TB results. A total of 191 systemic vasculitis patients were included and the positive rate of T-SPOT. TB was 31. 4%. The highest T-SPOT. TB positivity rate was observed in BehcE7et’s syndrome (BD) (72/191, 37. 7%). There were statistically significant differences between the LTBI group and non-LTBI group in terms of systemic vasculitis type (P = 0. 010), albumin levels (P = 0. 034), erythrocyte sedimentation rate (P = 0. 016), and corticosteroid dosage (P = 0. 047). Multivariate regression analysis revealed that smoking history (aOR = 3. 809, 95%CI: 1. 341-10. 817) and BD (aOR = 2. 106, 95%CI: 1. 042-4. 254) were independent risk factors of T-SPOT. TB postive results, besides decreased lymphocyte count (aOR = 0. 114, 95%CI: 0. 013-0. 973), and high-dose glucocorticoids use (aOR = 0. 386, 95%CI: 0. 149-1. 003) were independent risk factors of T-SPOT. TB negative results. The prevalence of LTBI is high in systemic vasculitis patients, especially those with BD or smoking history. Patients with decreased lymphocyte counts and high-dose glucocorticoid use are more likely to have a negative T-SPOT. TB results. Therefore, LTBI screening should be performed based on the characteristics of the patient during the diagnosis and treatment of systemic vasculitis. Key Points • We explored the positivity rate and risk factors of LTBI in systemic vasculitis patients from 13 hospitals in China. • There were 191 systemic vasculitis patients in our study. The positive rate of T-SPOT. TB was 31. 4%. The predominant type of systemic vasculitis was BD, with a T-SPOT. TB positive rate of 44. 4%. The second type was TA, with a T-SPOT. TB positive rate of 25. 0%. • The prevalence of LTBI is high in systemic vasculitis patients, especially those with BehcE7et’s syndrome or smoking history. Decreased lymphocyte counts and high-dose glucocorticoid use are more likely to have a negative T-SPOT. TB results. • LTBI screening using T-SPOT. TB should be conducted during the diagnosis and treatment of systemic vasculitis.

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Concepts Keywords
China Latent tuberculosis infection
Glucocorticoids Systemic vasculitis
Hospitals T-SPOT.TB
Tuberculosis

Semantics

Type Source Name
disease MESH Systemic vasculitis
disease MESH latent tuberculosis infection
disease MESH syndrome
disease IDO history
disease MESH tuberculosis
pathway KEGG Tuberculosis
disease MESH infection
disease IDO country
drug DRUGBANK Gold
disease IDO assay
drug DRUGBANK Coenzyme M
disease IDO pathogen
drug DRUGBANK Mycophenolate mofetil
drug DRUGBANK Methotrexate
drug DRUGBANK Azathioprine
drug DRUGBANK Leflunomide
drug DRUGBANK Sulfasalazine
drug DRUGBANK Etanercept
drug DRUGBANK Infliximab
disease MESH arthritis
disease MESH polyarteritis nodosa
disease MESH angiitis
drug DRUGBANK Medroxyprogesterone acetate
disease MESH arteritis
disease MESH tumor
disease MESH Behcet’s disease
disease IDO blood
disease IDO cell
drug DRUGBANK Urea
drug DRUGBANK Creatinine
drug DRUGBANK Cyclophosphamide
drug DRUGBANK Monomethyl fumarate
drug DRUGBANK Ciclosporin
drug DRUGBANK Tacrolimus
drug DRUGBANK Tripterygium wilfordii whole
drug DRUGBANK Adalimumab
drug DRUGBANK Tocilizumab
drug DRUGBANK Rituximab
drug DRUGBANK Trestolone
disease MESH opportunistic infections
disease MESH pulmonary tuberculosis
disease MESH HIV infection
pathway REACTOME HIV Infection
disease MESH diabetes mellitus
disease MESH rheumatic diseases
disease MESH silicosis
disease MESH chronic renal failure
disease MESH Takayasu arteritis
disease MESH defects
disease IDO immune response
disease MESH lymphocytopenia
disease MESH uncertainty
disease MESH malnutrition
disease IDO process
pathway REACTOME Reproduction
disease MESH retinal vasculitis
disease MESH systemic lupus erythematosus
pathway KEGG Systemic lupus erythematosus
disease IDO production
disease MESH copd
disease MESH tic
disease MESH covid 19
disease MESH uveitis
drug DRUGBANK Carboxyamidotriazole
disease MESH lymphadenopathy
disease MESH immune disease
drug DRUGBANK (S)-Des-Me-Ampa

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