Stortz Ethan, Lawler Helen
Division of Endocrinology, Metabolism, and Diabetes, University of Colorado School of Medicine, Aurora, CO 80045, USA.
JCEM Case Rep. 2024 Oct 23;2(11):luae194. doi: 10.1210/jcemcr/luae194. eCollection 2024 Nov.
Early dumping syndrome (DS) and postbariatric hypoglycemia (PBH) are challenging conditions with limited treatment options. A 46-year-old woman with prediabetes, obesity, and sleeve gastrectomy presented with digestive symptoms suggestive of DS and postprandial hypoglycemia consistent with PBH. She started tirzepatide 2.5 mg weekly, which decreased postprandial blood glucose peaks, increased postprandial blood glucose nadirs, and improved overall time in range on continuous glucose monitoring (CGM). Her postprandial bloating and diarrhea resolved. To our knowledge, there have been no reported cases of DS or PBH treated with dual-incretin agonists. While glucagon-like peptide-1 (GLP-1) agonists have not been widely attempted in DS and have shown mixed benefit for PBH, combination GLP-1 and gastric inhibitory peptide agonism may represent a novel treatment both for PBH and DS, providing greater improvement in glycemic variation as well as better DS control than GLP-1 agonism alone.
早期倾倒综合征(DS)和减重术后低血糖症(PBH)是具有挑战性的病症,治疗选择有限。一名46岁患有糖尿病前期、肥胖症且接受了袖状胃切除术的女性出现了提示DS的消化症状以及与PBH一致的餐后低血糖症。她开始每周注射2.5毫克替尔泊肽,这降低了餐后血糖峰值,提高了餐后血糖最低点,并改善了持续葡萄糖监测(CGM)期间的总体血糖达标时间。她的餐后腹胀和腹泻症状得到缓解。据我们所知,尚无使用双肠促胰岛素激动剂治疗DS或PBH的报道病例。虽然胰高血糖素样肽-1(GLP-1)激动剂在DS中尚未得到广泛尝试,且对PBH的益处不一,但GLP-1和胃抑制肽联合激动作用可能代表了一种针对PBH和DS的新型治疗方法,与单独使用GLP-1激动剂相比,在血糖波动方面有更大改善,对DS的控制也更好。