首页> 美国卫生研究院文献>Annals of the Rheumatic Diseases >Effects of prostaglandin E2 on disease activity gastric secretion and intestinal permeability and morphology in patients with rheumatoid arthritis.
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Effects of prostaglandin E2 on disease activity gastric secretion and intestinal permeability and morphology in patients with rheumatoid arthritis.

机译:前列腺素E2对类风湿关节炎患者疾病活性胃液分泌和肠道通透性以及形态的影响。

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摘要

The effects of oral natural prostaglandin E2 (PGE2) on symptoms, disease activity, and gastrointestinal functions in rheumatoid arthritis (RA) were studied in an open pilot trial. Twelve patients, six taking and six not taking non-steroidal anti-inflammatory drugs (NSAIDs), received 1 mg natural PGE2 three times a day for six weeks. The treatment was tolerated well and the only side effect noted was slightly looser stools in three patients. Half of the patients reported subjective improvement and none had aggravation of symptoms. The Ritchie articular index and several biochemical inflammation markers decreased and were significantly reduced at the end of the treatment period. The thickness of the small intestinal mucosa increased during the PGE2 treatment. The intestinal permeability pattern, measured by urinary excretion of polyethylene glycols (PEG 400), differed between the patients taking and not taking NSAIDs. The initially high urinary PEG 400 excretion values in the patients taking NSAIDs decreased and the initially low excretion values in patients not taking NSAIDs increased during the PGE2 treatment. The jejunal contents became sterile in 5/6 patients not taking NSAIDs and remained sterile in 1/6 patients taking NSAIDs at the end of the treatment. The treatment period was associated with a reduction of lactobacilli in patients not treated with NSAIDs. Thus the treatment appeared to decrease disease activity and to improve small intestinal functions in patients with RA, findings that need confirmation in a controlled trial.
机译:一项开放性试验研究了口服天然前列腺素E2(PGE2)对类风湿关节炎(RA)的症状,疾病活动和胃肠道功能的影响。 12名患者,其中6名服用和6名未服用非甾体类抗炎药(NSAID),每天接受1毫克天然PGE2,连续3周,共六周。治疗耐受性良好,唯一的副作用是三名患者的粪便稍松一些。半数患者报告主观好转,无症状加重。在治疗期结束时,Ritchie关节指数和一些生化炎症标志物降低并且显着降低。在PGE2治疗期间,小肠粘膜的厚度增加。通过服用聚乙二醇(PEG 400)的尿排泄量测得的肠道通透性模式在服用和不服用NSAID的患者之间有所不同。在PGE2治疗期间,服用NSAIDs的患者最初较高的尿PEG 400排泄值降低,而未服用NSAIDs的患者最初较低的排泄值增加。在治疗结束时,空肠内容物对不服用NSAIDs的5/6患者变为无菌,而对1/6服用NSAIDs的患者保持无菌。在未接受NSAID治疗的患者中,治疗期与乳酸菌减少有关。因此,这种治疗似乎降低了RA患者的疾病活动性并改善了小肠功能,这一发现需要在对照试验中得到证实。

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