Cited 16 times in
Intestinal Glycolysis Visualized by FDG PET/CT Correlates With Glucose Decrement After Gastrectomy
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 구철룡 | - |
dc.contributor.author | 윤미진 | - |
dc.contributor.author | 이나래 | - |
dc.contributor.author | 이은직 | - |
dc.contributor.author | 조응혁 | - |
dc.contributor.author | 형우진 | - |
dc.contributor.author | 노성훈 | - |
dc.date.accessioned | 2017-11-01T09:06:25Z | - |
dc.date.available | 2017-11-01T09:06:25Z | - |
dc.date.issued | 2017 | - |
dc.identifier.issn | 0012-1797 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/154023 | - |
dc.description.abstract | Gastrectomy method is known to influence glucose homeostasis. 18F-fluoro-2-fluorodeoxyglucose (FDG) positron emission tomography (PET)/computed tomography (CT) images acquired after gastrectomy often reveals newly developed physiological small bowel uptake. We correlated newly developed small bowel FDG uptake and glucose homeostasis in postgastrectomy gastric cancer patients. We retrospectively analyzed 239 patients without diabetes who underwent staging and follow-up FDG PET/CT scanning before and after gastrectomy for gastric cancer. Postoperative small bowel glycolysis was quantified by recording intestinal total lesion glycolysis (TLG). TLG was assessed with regard to surgical method (Billroth I, Billroth II [BII], Roux-en-Y [RY]), fasting glucose decrement (≥10 mg/dL), and other clinical factors. Patients' weight, fasting glucose, cholesterol, TLG, and body fat levels significantly decreased after surgery. The glucose decrement was significantly associated with fasting glucose, surgical methods, total cholesterol, TLG, and total body fat on univariate analysis. Multivariate analysis showed that BII surgery (odds ratio 6.51) and TLG (odds ratio 3.17) were significantly correlated with glucose decrement. High small bowel glycolysis (TLG >42.0 g) correlated with glucose decrement in RY patients. Newly developed small bowel glycolysis on postgastrectomy FDG PET/CT scanning is correlated with a glucose decrement. These findings suggest a potential role of FDG PET/CT scanning in the evaluation of small bowel glycolysis and glucose control. | - |
dc.description.statementOfResponsibility | restriction | - |
dc.language | English | - |
dc.publisher | American Diabetes Association | - |
dc.relation.isPartOf | DIABETES | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.subject.MESH | Aged | - |
dc.subject.MESH | Diabetes Mellitus/diagnostic imaging* | - |
dc.subject.MESH | Diabetes Mellitus/metabolism | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Fluorodeoxyglucose F18 | - |
dc.subject.MESH | Gastrectomy/methods* | - |
dc.subject.MESH | Glucose/metabolism* | - |
dc.subject.MESH | Glycolysis* | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Intestines/diagnostic imaging* | - |
dc.subject.MESH | Intestines/metabolism | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Multivariate Analysis | - |
dc.subject.MESH | Odds Ratio | - |
dc.subject.MESH | Positron Emission Tomography Computed Tomography | - |
dc.subject.MESH | Radiopharmaceuticals | - |
dc.subject.MESH | Retrospective Studies | - |
dc.subject.MESH | Stomach Neoplasms/surgery | - |
dc.title | Intestinal Glycolysis Visualized by FDG PET/CT Correlates With Glucose Decrement After Gastrectomy | - |
dc.type | Article | - |
dc.publisher.location | United States | - |
dc.contributor.college | College of Medicine | - |
dc.contributor.department | Dept. of Internal Medicine | - |
dc.contributor.googleauthor | Cheol Ryong Ku | - |
dc.contributor.googleauthor | Narae Lee | - |
dc.contributor.googleauthor | Jae Won Hong | - |
dc.contributor.googleauthor | In Gyu Kwon | - |
dc.contributor.googleauthor | Woo Jin Hyung | - |
dc.contributor.googleauthor | Sung Hoon Noh | - |
dc.contributor.googleauthor | Eun Jig Lee | - |
dc.contributor.googleauthor | Mijin Yun | - |
dc.contributor.googleauthor | Arthur Cho | - |
dc.identifier.doi | 10.2337/db16-1000 | - |
dc.contributor.localId | A02550 | - |
dc.contributor.localId | A02703 | - |
dc.contributor.localId | A03050 | - |
dc.contributor.localId | A03887 | - |
dc.contributor.localId | A04382 | - |
dc.contributor.localId | A01281 | - |
dc.contributor.localId | A00201 | - |
dc.relation.journalcode | J00718 | - |
dc.identifier.eissn | 1939-327X | - |
dc.identifier.pmid | 27903746 | - |
dc.identifier.url | http://diabetes.diabetesjournals.org/content/66/2/385.long | - |
dc.contributor.alternativeName | Ku, Cheol Ryong | - |
dc.contributor.alternativeName | Yun, Mi Jin | - |
dc.contributor.alternativeName | Lee, Na Rae | - |
dc.contributor.alternativeName | Lee, Eun Jig | - |
dc.contributor.alternativeName | Cho, Arthur Eung Hyuck | - |
dc.contributor.alternativeName | Hyung, Woo Jin | - |
dc.contributor.alternativeName | Noh, Sung Hoon | - |
dc.contributor.affiliatedAuthor | Yun, Mi Jin | - |
dc.contributor.affiliatedAuthor | Lee, Na Rae | - |
dc.contributor.affiliatedAuthor | Lee, Eun Jig | - |
dc.contributor.affiliatedAuthor | Cho, Arthur Eung Hyuck | - |
dc.contributor.affiliatedAuthor | Hyung, Woo Jin | - |
dc.contributor.affiliatedAuthor | Noh, Sung Hoon | - |
dc.contributor.affiliatedAuthor | Ku, Cheol Ryong | - |
dc.citation.title | Diabetes | - |
dc.citation.volume | 66 | - |
dc.citation.number | 2 | - |
dc.citation.startPage | 385 | - |
dc.citation.endPage | 391 | - |
dc.identifier.bibliographicCitation | DIABETES, Vol.66(2) : 385-391, 2017 | - |
dc.date.modified | 2017-11-01 | - |
dc.identifier.rimsid | 44192 | - |
dc.type.rims | ART | - |
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