Bharucha A E, Daley S L, Low P A, Gibbons S J, Choi K M, Camilleri M, Saw J J, Farrugia G, Zinsmeister A R
Enteric Neurosciences Program, Division of Gastroenterology and Hepatology, Department of Medicine, Mayo Clinic, Rochester, MN, USA.
Department of Neurology, Mayo Clinic, Rochester, MN, USA.
Neurogastroenterol Motil. 2016 Nov;28(11):1731-1740. doi: 10.1111/nmo.12874. Epub 2016 Jun 9.
Therapeutic options for management of diabetic gastroparesis are limited. Failure to maintain upregulation of heme oxygenase (HO1) leads to loss of interstitial cells of Cajal and delayed gastric emptying (GE) in non-obese diabetic mice. Our hypothesis was that hemin upregulation of HO1 would restore normal GE in humans with gastroparesis.
To compare effects of hemin and placebo infusions on HO1 activity and protein, GE, autonomic function, and gastrointestinal symptoms in diabetic gastroparesis.
In a single-center, double-blind, placebo-controlled, randomized clinical trial, we compared intravenous hemin, prepared in albumin, or albumin alone (placebo) in 20 patients, aged 41 ± 5 (SEM) years with diabetic gastroparesis. After infusions on days 1, 3, and 7, weekly infusions were administered for 7 additional weeks. Assessments included blood tests for HO1 protein and enzyme activity levels, GE with C-spirulina breath test, autonomic functions (baseline and end), and gastrointestinal symptoms every 2 weeks.
Nine of 11 patients randomized to hemin completed all study procedures. Compared to placebo, hemin increased HO1 protein on days 3 (p = 0.0002) and 7 (p = 0.008) and HO1 activity on day 3 (p = 0.0003) but not after. Gastric emptying, autonomic functions, and symptoms did not differ significantly in the hemin group relative to placebo.
CONCLUSIONS & INFERENCES: Hemin failed to sustain increased HO1 levels beyond a week and did not improve GE or symptoms in diabetic gastroparesis. Further studies are necessary to ascertain whether more frequent hemin infusions or other drugs would have a more sustained effect on HO1 and improve GE.
糖尿病性胃轻瘫的治疗选择有限。在非肥胖糖尿病小鼠中,未能维持血红素加氧酶(HO1)的上调会导致 Cajal 间质细胞丢失和胃排空延迟(GE)。我们的假设是,血红素上调 HO1 可恢复胃轻瘫患者的正常胃排空。
比较血红素和安慰剂输注对糖尿病性胃轻瘫患者 HO1 活性、蛋白质、胃排空、自主神经功能和胃肠道症状的影响。
在一项单中心、双盲、安慰剂对照、随机临床试验中,我们比较了 20 例年龄为 41±5(SEM)岁的糖尿病性胃轻瘫患者静脉输注白蛋白配制的血红素或单独输注白蛋白(安慰剂)的效果。在第 1、3 和 7 天输注后,再每周输注 7 周。评估包括检测 HO1 蛋白和酶活性水平的血液检查、用 C-螺旋藻呼气试验检测胃排空、自主神经功能(基线和结束时)以及每 2 周评估一次胃肠道症状。
随机分配到血红素组的 11 名患者中有 9 名完成了所有研究程序。与安慰剂相比,血红素在第 3 天(p = 0.0002)和第 7 天(p = 0.008)增加了 HO1 蛋白,在第 3 天增加了 HO1 活性(p = 0.0003),但之后没有增加。血红素组的胃排空、自主神经功能和症状与安慰剂组相比无显著差异。
血红素未能使 HO1 水平升高超过一周,也未改善糖尿病性胃轻瘫的胃排空或症状。有必要进一步研究以确定更频繁地输注血红素或其他药物是否会对 HO1 产生更持久的影响并改善胃排空。