Microbiology and Mycology Program, Institute of Biomedical Sciences, Faculty of Medicine, Universidad de Chile, Santiago, Chile.
Department of Pediatrics and Pediatric Surgery (Northern Campus), Hospital Dr. Roberto del Río Hospital, Faculty of Medicine, Universidad de Chile, Santiago, Chile.
Helicobacter. 2021 Dec;26(6):e12853. doi: 10.1111/hel.12853. Epub 2021 Sep 15.
Helicobacter pylori (H. pylori) is the primary cause of gastric cancer and eradication in healthy adults has proven effective in decreasing cancer incidence. H. pylori is acquired largely in early childhood, however, the benefits of eradication in children are controversial. We aimed to determine the effect of H. pylori eradication on clinical and laboratory markers associated with gastric damage in apparently healthy school-aged children.
This was a pilot non-blinded trial including 61 children persistently infected with H. pylori who were randomized to eradication/no treatment and followed for at least 12 months, evaluating clinical and blood markers (Pepsinogen I (PGI) and II (PGII) determined by ELISA) associated with gastric damage. The treatment consisted of a sequential scheme including 7 days of omeprazole + amoxicillin followed by 7 days of omeprazole + clarithromycin + metronidazole; adherence and tolerance were surveyed. Eradication rates were assessed by stool antigen detection or urea breath test 1 month following treatment every 4 months thereafter to detect reinfection.
Eradication occurred in 30/31 treated children (median age: 8.8, range: 7.9-10.8) and in 0/30 non-treated controls (median age: 8.6, range: 7.9-11) (p < .001). Treatment was associated with mild transient symptoms (altered taste, nocturnal upper abdominal pain, nausea, and diarrhea). Baseline frequency of symptoms was low and eradication did not change symptoms compared to controls. PGI, PGII, and anti-H. pylori seropositivity were similar in both groups at baseline and significantly decreased only in eradicated patients; PGI (92.5 vs. 74.4, p < .001), PGII (15.2 vs. 8.9, p < .001) levels, and frequency of anti-H. pylori seropositivity (100 vs. 68%, p < .001) respectively. Four eradicated children (13%) were reinfected during follow-up.
H. pylori eradication therapy in apparently asymptomatic school-aged children was well tolerated and associated with decreased serum PGI and PGII levels. Future studies should expand on the middle-long-term effect of early H. pylori eradication, especially on preventing gastric cancer.
幽门螺杆菌(H. pylori)是胃癌的主要病因,在健康成年人中根除 H. pylori 已被证明可有效降低癌症发病率。H. pylori 主要在儿童早期获得,但根除 H. pylori 在儿童中的益处存在争议。我们旨在确定根除 H. pylori 对与胃损伤相关的临床和实验室标志物在明显健康的学龄儿童中的影响。
这是一项非盲试点试验,纳入 61 例持续感染 H. pylori 的儿童,随机分为根除/无治疗组,并至少随访 12 个月,评估与胃损伤相关的临床和血液标志物(通过 ELISA 测定胃蛋白酶原 I(PGI)和 II(PGII))。治疗包括一个序贯方案,包括 7 天奥美拉唑+阿莫西林,然后是 7 天奥美拉唑+克拉霉素+甲硝唑;调查了依从性和耐受性。治疗后 1 个月进行粪便抗原检测或尿素呼气试验,此后每 4 个月进行一次,以检测再感染。
31 例接受治疗的儿童中有 30 例(中位年龄:8.8 岁,范围:7.9-10.8)和 30 例未接受治疗的对照组中均无(中位年龄:8.6 岁,范围:7.9-11)(p <.001)根除。治疗与轻度短暂症状相关(味觉改变、夜间上腹痛、恶心和腹泻)。基线症状频率较低,根除治疗与对照组相比并未改变症状。PGI、PGII 和抗 H. pylori 血清阳性率在两组基线时相似,仅在根除患者中显著降低;PGI(92.5 与 74.4,p <.001)、PGII(15.2 与 8.9,p <.001)水平和抗 H. pylori 血清阳性率(100 与 68%,p <.001)分别。在随访期间,有 4 例根除儿童(13%)被再感染。
在无症状的学龄儿童中,根除 H. pylori 治疗耐受性良好,与血清 PGI 和 PGII 水平降低有关。未来的研究应扩大早期根除 H. pylori 的中-长期效果,特别是预防胃癌的效果。