Tie Kevin, Aboueisha Mohamed A, Wang Madelyn, Caradonna David S, Brook Christopher D
Department of Otolaryngology-Head & Neck Surgery, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.
Renaissance School of Medicine at Stony Brook University, Stony Brook, NY 11794, USA.
Am J Otolaryngol. 2025 Jan-Feb;46(1):104541. doi: 10.1016/j.amjoto.2024.104541. Epub 2024 Dec 4.
Primary immunodeficiency has been associated with chronic rhinosinusitis (CRS). However, limited evidence exists on how primary immunodeficiencies affect the severity of CRS.
To assess how primary IgA and/or IgG immunodeficiency affects the severity of CRS.
Adult patients at the Beth Israel Deaconess Medical Center in Boston with IgA and/or IgG deficiency (group A) or normal IgA and IgG (group B) were queried between January 1, 2016 and December 31, 2022. Other immunodeficiencies were excluded. The groups were analyzed for prevalence of CRS based on ICD-10 codes. The groups were matched based on demographics and comorbidities. Patients with CRS were analyzed for ≥3 acute rhinosinusitis (ARS) episodes, mean lifetime ARS episodes, and mean ARS episodes per year (all with or without antibiotic treatment). Additional analyses included need for functional endoscopic sinus surgery (FESS) and mean lifetime FESS procedures based on CPT codes. A logistic regression analysis was then performed over the same parameters.
A total of 346 patients had IgA and/or IgG deficiency (group A), and 11,438 patients had normal IgA and IgG (group B). CRS prevalence was higher in group A than group B (12 % vs. 5 %; p < 0.001). Group A had more patients with ≥3 ARS episodes, higher mean lifetime ARS episodes, and ARS episodes per year, though none of these findings were statistically significant. There was no difference in need for FESS or mean lifetime FESS procedures.
CRS prevalence is higher in patients with IgA and/or IgG deficiency, but IgA and/or IgG immunodeficiency does not predispose patients to ARS episodes or predict need for FESS.
原发性免疫缺陷与慢性鼻-鼻窦炎(CRS)相关。然而,关于原发性免疫缺陷如何影响CRS严重程度的证据有限。
评估原发性IgA和/或IgG免疫缺陷如何影响CRS的严重程度。
2016年1月1日至2022年12月31日期间,对波士顿贝斯以色列女执事医疗中心的成年患者进行了调查,这些患者存在IgA和/或IgG缺乏(A组)或IgA和IgG正常(B组)。排除其他免疫缺陷。根据国际疾病分类第十版(ICD-10)编码分析两组CRS的患病率。根据人口统计学和合并症对两组进行匹配。对患有CRS的患者分析≥3次急性鼻-鼻窦炎(ARS)发作、平均终生ARS发作次数以及每年平均ARS发作次数(均包括或不包括抗生素治疗)。其他分析包括基于现行程序术语(CPT)编码的功能性内镜鼻窦手术(FESS)需求和平均终生FESS手术次数。然后对相同参数进行逻辑回归分析。
共有346例患者存在IgA和/或IgG缺乏(A组),11438例患者IgA和IgG正常(B组)。A组CRS患病率高于B组(12%对5%;p<0.001)。A组中≥3次ARS发作的患者更多,平均终生ARS发作次数和每年ARS发作次数更高,尽管这些结果均无统计学意义。FESS需求或平均终生FESS手术次数没有差异。
IgA和/或IgG缺乏患者的CRS患病率较高,但IgA和/或IgG免疫缺陷并不会使患者易患ARS发作或预测FESS需求。