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<article xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML" article-type="letter"><?properties open_access?><front><journal-meta><journal-id journal-id-type="nlm-ta">Korean J Intern Med</journal-id><journal-id journal-id-type="iso-abbrev">Korean J. Intern. Med</journal-id><journal-id journal-id-type="publisher-id">KJIM</journal-id><journal-title-group><journal-title>The Korean Journal of Internal Medicine</journal-title></journal-title-group><issn pub-type="ppub">1226-3303</issn><issn pub-type="epub">2005-6648</issn><publisher><publisher-name>The Korean Association of Internal Medicine</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">23346005</article-id><article-id pub-id-type="pmc">3543949</article-id><article-id pub-id-type="doi">10.3904/kjim.2013.28.1.106</article-id><article-categories><subj-group subj-group-type="heading"><subject>Letter to the Editor</subject></subj-group></article-categories><title-group><article-title>Ramosetron might be useful for treating diabetic diarrhea with a rapid small bowel transit time</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Lee</surname><given-names>Tae Hee</given-names></name><xref ref-type="aff" rid="A1-kjim-28-106"/></contrib><contrib contrib-type="author" corresp="yes"><name><surname>Lee</surname><given-names>Joon Seong</given-names></name><xref ref-type="aff" rid="A1-kjim-28-106"/></contrib></contrib-group><aff id="A1-kjim-28-106">Institute for Digestive Research, Soonchunhyang University College of Medicine, Seoul, Korea.</aff><author-notes><corresp>
Correspondence to Joon Seong Lee, M.D. Institute for Digestive Research, Soonchunhyang University College of Medicine, 59 Daesagwan-ro, Yongsan-gu, Seoul 140-743, Korea. Tel: +82-2-709-9691, Fax: +82-2-709-9696, <email>drjslee@dreamwiz.com</email></corresp></author-notes><pub-date pub-type="ppub"><month>1</month><year>2013</year></pub-date><pub-date pub-type="epub"><day>28</day><month>12</month><year>2012</year></pub-date><volume>28</volume><issue>1</issue><fpage>106</fpage><lpage>107</lpage><history><date date-type="received"><day>19</day><month>3</month><year>2012</year></date><date date-type="rev-recd"><day>13</day><month>9</month><year>2012</year></date><date date-type="accepted"><day>24</day><month>9</month><year>2012</year></date></history><permissions><copyright-statement>Copyright &#xA9; 2013 The Korean Association of Internal Medicine</copyright-statement><copyright-year>2013</copyright-year><license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by-nc/3.0/"><license-p>This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by-nc/3.0/">http://creativecommons.org/licenses/by-nc/3.0/</ext-link>) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p></license></permissions><kwd-group><kwd>Diabetes</kwd><kwd>Diarrhea</kwd><kwd>Ramosetron</kwd></kwd-group></article-meta></front><body><p>To the Editor,</p><p>The diagnosis and treatment of diarrhea can be challenging. Diabetic diarrhea is seen mainly in patients with poorly controlled insulin-dependent diabetes who also have symptoms of diabetic peripheral and autonomic neuropathy. Typically, the diarrhea is painless, occurs during the day and night, and may be associated with fecal incontinence [<xref ref-type="bibr" rid="B1-kjim-28-106">1</xref>]. We used ramosetron, a selective 5-HT<sub>3</sub> receptor antagonist, to treat diabetic diarrhea with a rapid small bowel transit time.</p><p>A 49-year-old man who had developed type 2 diabetes mellitus at 42 years of age, presented with diarrhea 6 months ago. His glycemia was poorly controlled, based on a haemoglobin A1c of 17.7%. He had hypercholesterolemia, orthostatic hypotension, diabetic retinopathy, nephropathy, peripheral neuropathy, autonomic neuropathy, and gastroparesis. Current medications included insulin, losartan, atorvastatin, midodrine, metoclopramide, and domperidone. Diarrhea occurred at a frequency of &gt; 10 bowel movements per day, with fecal urgency following meals. Steatorrhea was absent and the stool examination was unremarkable. He was prescribed conventional antidiarrheals, including a pancreatic enzyme supplement, rifaximin, probiotics, cimetropium bromide, and loperamide, but these were ineffective. He also had iron-deficiency anemia, as evidenced by a hemoglobin of 9.1 g/dL, mean corpuscular volume of 84.7 fL, 1.95% reticulocytes, and ferritin of 8.45 ng/mL. Capsule endoscopy (PillCam SB2, Given Imaging, Yokneam, Israel) was performed after upper endoscopy, colonoscopy, and abdominal computed tomography failed to explain the iron-deficiency anemia. He fasted for 12 hours before capsule ingestion. For 4 hours following ingestion of the capsule, only water was permitted, after which a liquid diet was offered. All medications except the losartan were discontinued. Capsule endoscopy identified multiple angiodysplastic lesions in the distal ileum. Interestingly, a markedly prolonged gastric emptying time (13 hours 33 minutes) with a rapid small bowel transit time (14 minutes) was noted (<xref ref-type="fig" rid="F1-kjim-28-106">Fig. 1</xref>), suggesting gastroparesis and autonomic neuropathy, respectively. The diarrhea persisted, so ramosetron therapy (Irribow, Astellas Pharma Korea, Seoul, Korea) was started at 5 &#xB5;g once daily before breakfast. The diarrhea and fecal urgency disappeared completely after 1 week of ramosetron treatment, with the bowel movement frequency reduced to two soft stools per day. On ceasing ramosetron, the diarrhea recurred, but was relieved once more when the medication was restarted. 5-Hydroxytrytamine (5-HT) acts on 5-HT<sub>3</sub> parasympathetic receptors to produce smooth muscle contraction and the release of acetylcholine from nerve terminals, causing intestinal secretion to increase [<xref ref-type="bibr" rid="B2-kjim-28-106">2</xref>]. The 5-HT<sub>3</sub> receptor antagonist alosetron is useful in the treatment of diarrhea in patients with irritable bowel syndrome, but must be avoided in more severe cases because of the risk of constipation [<xref ref-type="bibr" rid="B3-kjim-28-106">3</xref>]. The efficacy of other 5-HT3 receptor antagonists such as ondansetron [<xref ref-type="bibr" rid="B4-kjim-28-106">4</xref>] and ramosetron [<xref ref-type="bibr" rid="B5-kjim-28-106">5</xref>] in the treatment of diabetic diarrhea has been documented.</p><p>In conclusion, given the inhibitory effects of a 5-HT<sub>3</sub> receptor antagonist on smooth muscle contraction and secretion, ramosetron should be considered in cases of diabetic diarrhea with rapid small bowel transit. A larger study is needed to verify the efficacy of ramosetron in treating this condition.</p></body><back><fn-group><fn fn-type="conflict"><p>No potential conflict of interest relevant to this article is reported.</p></fn></fn-group><ref-list><ref id="B1-kjim-28-106"><label>1</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Ogbonnaya</surname><given-names>KI</given-names></name><name><surname>Arem</surname><given-names>R</given-names></name></person-group><article-title>Diabetic diarrhea: pathophysiology, diagnosis, and management</article-title><source>Arch Intern Med</source><year>1990</year><volume>150</volume><fpage>262</fpage><lpage>267</lpage><pub-id pub-id-type="pmid">2405798</pub-id></element-citation></ref><ref id="B2-kjim-28-106"><label>2</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Gershon</surname><given-names>MD</given-names></name></person-group><article-title>Review article: roles played by 5-hydroxytryptamine in the physiology of the bowel</article-title><source>Aliment Pharmacol Ther</source><year>1999</year><volume>13</volume><issue>Suppl 2</issue><fpage>15</fpage><lpage>30</lpage><pub-id pub-id-type="pmid">10429737</pub-id></element-citation></ref><ref id="B3-kjim-28-106"><label>3</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Cremonini</surname><given-names>F</given-names></name><name><surname>Delgado-Aros</surname><given-names>S</given-names></name><name><surname>Camilleri</surname><given-names>M</given-names></name></person-group><article-title>Efficacy of alosetron in irritable bowel syndrome: a meta-analysis of randomized controlled trials</article-title><source>Neurogastroenterol Motil</source><year>2003</year><volume>15</volume><fpage>79</fpage><lpage>86</lpage><pub-id pub-id-type="pmid">12588472</pub-id></element-citation></ref><ref id="B4-kjim-28-106"><label>4</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Bossi</surname><given-names>A</given-names></name><name><surname>Baresi</surname><given-names>A</given-names></name><name><surname>Ballini</surname><given-names>A</given-names></name><name><surname>Bindelli</surname><given-names>C</given-names></name></person-group><article-title>Ondasentron in the treatment of diabetic diarrhea</article-title><source>Diabetes Care</source><year>1994</year><volume>17</volume><fpage>453</fpage><lpage>454</lpage><pub-id pub-id-type="pmid">8062617</pub-id></element-citation></ref><ref id="B5-kjim-28-106"><label>5</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Murao</surname><given-names>S</given-names></name><name><surname>Hosokawa</surname><given-names>H</given-names></name></person-group><article-title>Serotonin 5-HT3 receptor antagonist for treatment of severe diabetic diarrhea</article-title><source>Diabetes Care</source><year>2010</year><volume>33</volume><fpage>e38</fpage><pub-id pub-id-type="pmid">20190286</pub-id></element-citation></ref></ref-list></back><floats-group><fig id="F1-kjim-28-106" position="float"><label>Figure 1</label><caption><p>(A) Stomach. (B) Duodenum. (C) Colon. Capsule endoscopy revealed a markedly prolonged gastric transit time with rapid small bowel transit (gastric emptying time, 13 hours 33 minutes; small bowel transit time, 14 minutes).</p></caption><graphic xlink:href="kjim-28-106-g001"/></fig></floats-group></article>
