Retrospective study uncovers distinct clinical features and genetic markers in severe antithyroid drug-induced agranulocytosis, indicating increased risk linked to HLA-B*38:02.
Agranulocytosis is a rare but serious side effect of antithyroid drugs (ATDs), defined by an absolute neutrophil count (ANC) below 500/μL; some patients develop a more severe form with ANC below 100/μL. We retrospectively compared the clinical, biochemical, and HLA‐B allele profiles between the two presentations in 24 cases of ATD‐induced agranulocytosis. Based on nadir ANC, 15 participants with ANC < 100/μL formed the severe group and 9 with ANC 100–500/μL comprised the typical group. The severe group had a significantly longer neutrophil recovery time (5 [5–7] vs. 3 [2.5–3.5] days; P = 0.003), higher median levels of total bilirubin (21.4 [13.3–30.4] vs. 7.1 [6.2–18.3] μmol/L; P = 0.003) and indirect bilirubin (9.9 [7.6–16.7] vs. 6.1 [3.6–9.8] μmol/L; P = 0.018), and fewer asymptomatic patients at presentation (0/15 vs. 5/9, P = 0.003). HLA typing confirmed that HLA‐B*38:02 was associated with severe ATD‐induced agranulocytosis (OR = 48.6; 95% CI = 2.3–1020.7; P = 5.9 × 10 −4 ). Sensitivity analysis excluding the 2 PTU‐treated patients confirmed a robust and significant association (OR = 38.3; 95% CI = 1.8–820.2; P = 0.0039). No significant differences were observed in age, sex, drug type or dosage, or other biochemical parameters at agranulocytosis onset. Severe agranulocytosis accounted for 62.5% (15/24) of cases, highlighting it as a common clinical phenotype of ATD‐induced agranulocytosis. HLA‐B*38:02 is associated with susceptibility to ATD‐induced severe agranulocytosis, an association predominantly driven by methimazole exposure.
No takes yet. Share an insight, caveat, or question.
Mao et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: