Department of Internal Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Dig Dis Sci. 2011 Nov;56(11):3254-61. doi: 10.1007/s10620-011-1754-3. Epub 2011 Jun 8.
Hypereosinophilic syndrome (HES) is defined by significant eosinophilia (>1,500 eos/μl), which often leads to end-organ damage/dysfunction. It is unclear if the presence of significant peripheral eosinophilia (>1,500 eos/μl) indicates a more aggressive form of eosinophilic gastrointestinal disorder (EGID).
A database query of the Mayo Clinic Rochester electronic records (1995-2008) was performed using several search terms for eosinophilic gastrointestinal disease, and 161 records were reviewed. Patients under 18 years age, those without Mayo-reviewed pathology specimens, those with eosinophilic esophagitis only, and/or those with evidence of secondary etiologies for GI eosinophilia were excluded. A total of 39 were found to have primary EGID. We compared individuals with biopsy-proven primary EGID based on whether they had significant peripheral eosinophilia (≥1,500 eos/μl) (group A) or not (group B).
Group A tended to have more atopy (A: 12/15; B: 11/24; p = 0.03) and more extensive segmental involvement of the GI tract (p = 0.001). None with available studies had evidence of cardiac (A: 7/15; B: 6/24) or bone marrow (A: 10/15; B: 6/24) involvement. The two thromboembolic events in group A after diagnosis did not translate to significantly greater risk (HR = infinity, p = 0.13; group A vs. B). Doses of initial (A: 40 mg/day; B: 55 mg/day; p = 0.17) and maintenance prednisone (A; 8.75 mg/day; B: 7.5 mg/day; p > 0.90) were similar. Group A was significantly more likely to need maintenance prednisone (77 vs. 8%, p = 0.001), with a median treatment duration of 52 weeks. Recurrence of symptoms (and peripheral eosinophilia) during prednisone taper was common in both groups. Prednisone-sparing agents (hydroxyurea, imatinib mesylate, interferon (IFN)-α2b, anti-interleukin (IL-5) monoclonal antibody) were more commonly used in group A (73 vs. 8%; p < 0.0001).
EGID with peripheral eosinophilia ≥1,500/μl is associated with atopy, greater GI segmental involvement, and uncertain risk of thrombosis. The common use of long-term steroids and variable responsiveness to nonsteroidal agents, particularly in group A, underscores the need for targeted therapies.
嗜酸性粒细胞增多症(HES)的定义为显著的嗜酸性粒细胞增多症(>1,500 个/μl),这通常会导致终末器官损伤/功能障碍。目前尚不清楚外周血显著嗜酸性粒细胞增多症(>1,500 个/μl)是否表示嗜酸性粒细胞性胃肠病(EGID)的更具侵袭性形式。
使用几个搜索术语对梅奥诊所罗彻斯特电子记录(1995-2008 年)进行数据库查询,共审查了 161 条记录。排除了年龄在 18 岁以下的患者、没有梅奥审查病理标本的患者、仅有嗜酸性食管炎的患者和/或有胃肠道嗜酸性粒细胞增多的继发性病因证据的患者。总共发现 39 例患有原发性 EGID。我们比较了基于活检证实的原发性 EGID 患者是否存在外周血嗜酸性粒细胞增多症(≥1,500 个/μl)(A 组)或不存在(B 组)。
A 组往往有更多的过敏症(A:12/15;B:11/24;p=0.03)和更广泛的胃肠道节段受累(p=0.001)。有可用研究的患者均无心脏(A:7/15;B:6/24)或骨髓(A:10/15;B:6/24)受累的证据。A 组在诊断后的两次血栓栓塞事件并未导致更高的风险(HR=无限,p=0.13;A 组与 B 组)。初始(A:40mg/天;B:55mg/天;p=0.17)和维持泼尼松(A;8.75mg/天;B:7.5mg/天;p>0.90)的剂量相似。A 组更有可能需要维持泼尼松(77%比 8%,p=0.001),中位治疗时间为 52 周。两组在泼尼松减量期间症状(和外周血嗜酸性粒细胞增多症)复发均很常见。A 组更常使用泼尼松节约药物(羟基脲、甲磺酸伊马替尼、干扰素(IFN)-α2b、抗白细胞介素(IL)-5 单克隆抗体)(73%比 8%;p<0.0001)。
外周血嗜酸性粒细胞增多症≥1,500/μl 的 EGID 与过敏症、更大的胃肠道节段受累以及血栓形成的不确定风险相关。长期使用类固醇和对非甾体药物反应的差异,特别是在 A 组,突显了靶向治疗的必要性。