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ACOMS+ 및 학술지 리포지터리 설명회

  • 한국과학기술정보연구원(KISTI) 서울분원 대회의실(별관 3층)
  • 2024년 07월 03일(수) 13:30
 

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비만 환자에서 리라글루티드 증량 과정에서 발생한 급성 신손상

Acute Kidney Injury after Dose-Titration of Liraglutide in an Obese Patient

비만대사연구학술지 / Archives of Obesity and Metabolism, (P)2951-0333; (E)2951-0597
2022, v.1 no.2, pp.78-82
https://doi.org/10.23137/AOM22.02.CR0004
이희진(Hee Jin Lee) (울산대학교 의과대학 서울아산병원 가정의학과)
박혜순(Hye Soon Park) (울산대학교 의과대학 서울아산병원 가정의학과)
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Abstract

Liraglutide (SaxendaR) is prescribed to induce and sustain weight loss in obese patients. The starting dose of liraglutide is 0.6 mg/day for 1 week, which is increased by 0.6 mg/day every week until the full maintenance dose of 3 mg/day is achieved.Such dose titration is needed to prevent side effects, which primarily include gastrointestinal problems such as nausea, diarrhea, constipation, vomiting, dyspepsia, and abdominal pain. A 35-year-old, reportedly healthy obese man receiving liraglutidetreatment for obesity visited the emergency room complaining of generalized weakness and dizziness accompanied by repeated diarrhea and vomiting. He reported over 20 episodes of diarrhea starting the day after liraglutide dose escalation from 1.2 mg/day to 1.8 mg/day. Laboratory findings suggested pre-renal acute kidney injury, including serum creatinine 4.77 mg/dl, blood urea nitrogen (BUN) 37 mg/dl, estimated glomerular filtration rate (eGFR) 15 ml/min/1.73 m2, and Fractional excretion of sodium 0.08. After volume repletion therapy, his renal function recovered to a normal range with laboratory values of creatinine 1.08 mg/dl, BUN 14 mg/dl, and eGFR 88ml/min/1.73 m2. This case emphasizes the need for caution when prescribing glucagon-like peptide-1 receptor agonists, including liraglutide, given the risk of serious renal impairments induced by volume depletion and dehydration through severegrade diarrhea and vomiting.

keywords
Obesity, Liraglutide, Side effects, Acute kidney injury

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