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Serum fibroblast growth factor-21 concentration is associated with residual renal function and insulin resistance in end-stage renal disease patients receiving long-term peritoneal dialysis
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | 강신욱 | - |
| dc.contributor.author | 한대석 | - |
| dc.contributor.author | 한승혁 | - |
| dc.date.accessioned | 2015-04-23T17:42:38Z | - |
| dc.date.available | 2015-04-23T17:42:38Z | - |
| dc.date.issued | 2010 | - |
| dc.identifier.issn | 0026-0495 | - |
| dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/102981 | - |
| dc.description.abstract | Fibroblast growth factor-21 (FGF-21) is a new metabolic regulator, which is related to antiobesity and insulin sensitivity in vivo. However, the clinical implication of FGF-21 is poorly understood. To investigate whether FGF-21 may play a role as a metabolic regulator in patients with end-stage renal disease, we measured serum concentrations of FGF-21, inflammatory markers, and metabolic parameters in healthy people (n = 63) and nondiabetic patients receiving peritoneal dialysis (PD, n = 72). The patients were treated with angiotensin receptor blocker for 6 months, and the changes in FGF-21 concentration and metabolic parameters were assessed. Compared with controls, serum FGF-21 concentration was 8 times higher in patients undergoing PD (754.2 ± 463.5 vs 86.9 ± 60.2 pg/mL, P < .001). In controls, only lipid parameters correlated positively with FGF-21 concentration. In contrast, inflammatory markers (interleukin-6, fibrinogen, high-sensitivity C-reactive protein) and homeostasis model assessment of insulin resistance (HOMA-IR) correlated positively and residual renal function correlated inversely with serum FGF-21 concentration in PD patients. In a multivariate analysis adjusting these factors, residual renal function, HOMA-IR, and fibrinogen concentration were independent determinants of serum FGF-21 concentration. After 6-month angiotensin receptor blocker treatment, serum FGF-21 concentration declined significantly by 13% and HOMA-IR and inflammatory markers improved in PD patients. These findings suggest that FGF-21 may play a role in insulin resistance in patients with end-stage renal disease | - |
| dc.description.statementOfResponsibility | open | - |
| dc.format.extent | 1656~1662 | - |
| dc.relation.isPartOf | METABOLISM-CLINICAL AND EXPERIMENTAL | - |
| 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 | Adult | - |
| dc.subject.MESH | Angiotensin Receptor Antagonists/administration & dosage | - |
| dc.subject.MESH | Angiotensin Receptor Antagonists/pharmacology | - |
| dc.subject.MESH | Angiotensin Receptor Antagonists/therapeutic use | - |
| dc.subject.MESH | Biomarkers | - |
| dc.subject.MESH | Case-Control Studies | - |
| dc.subject.MESH | Female | - |
| dc.subject.MESH | Fibrinogen/analysis | - |
| dc.subject.MESH | Fibroblast Growth Factors/blood* | - |
| dc.subject.MESH | Fibroblast Growth Factors/drug effects | - |
| dc.subject.MESH | Fibroblast Growth Factors/metabolism | - |
| dc.subject.MESH | Humans | - |
| dc.subject.MESH | Inflammation | - |
| dc.subject.MESH | Insulin Resistance* | - |
| dc.subject.MESH | Kidney/physiopathology* | - |
| dc.subject.MESH | Kidney Failure, Chronic/blood* | - |
| dc.subject.MESH | Kidney Failure, Chronic/therapy | - |
| dc.subject.MESH | Male | - |
| dc.subject.MESH | Middle Aged | - |
| dc.subject.MESH | Peritoneal Dialysis* | - |
| dc.title | Serum fibroblast growth factor-21 concentration is associated with residual renal function and insulin resistance in end-stage renal disease patients receiving long-term peritoneal dialysis | - |
| dc.type | Article | - |
| dc.contributor.college | College of Medicine (의과대학) | - |
| dc.contributor.department | Dept. of Internal Medicine (내과학) | - |
| dc.contributor.googleauthor | Seung Hyeok Han | - |
| dc.contributor.googleauthor | Sung Hee Choi | - |
| dc.contributor.googleauthor | Bong Jun Cho | - |
| dc.contributor.googleauthor | Yenna Lee | - |
| dc.contributor.googleauthor | Soo Lim | - |
| dc.contributor.googleauthor | Young Joo Park | - |
| dc.contributor.googleauthor | Min Kyung Moon | - |
| dc.contributor.googleauthor | Hong Kyu Lee | - |
| dc.contributor.googleauthor | Shin-Wook Kang | - |
| dc.contributor.googleauthor | Dae Suk Han | - |
| dc.contributor.googleauthor | Young-Bum Kim | - |
| dc.contributor.googleauthor | Hak C. Jang | - |
| dc.contributor.googleauthor | Kyong Soo Park | - |
| dc.identifier.doi | 10.1016/j.metabol.2010.03.018 | - |
| dc.admin.author | false | - |
| dc.admin.mapping | false | - |
| dc.contributor.localId | A00053 | - |
| dc.contributor.localId | A04272 | - |
| dc.contributor.localId | A04304 | - |
| dc.relation.journalcode | J02223 | - |
| dc.identifier.eissn | 1532-8600 | - |
| dc.identifier.pmid | 20423749 | - |
| dc.identifier.url | http://www.sciencedirect.com/science/article/pii/S0026049510001083 | - |
| dc.contributor.alternativeName | Kang, Shin Wook | - |
| dc.contributor.alternativeName | Han, Dae Suk | - |
| dc.contributor.alternativeName | Han, Seung Hyeok | - |
| dc.contributor.affiliatedAuthor | Kang, Shin Wook | - |
| dc.contributor.affiliatedAuthor | Han, Dae Suk | - |
| dc.contributor.affiliatedAuthor | Han, Seung Hyeok | - |
| dc.citation.volume | 59 | - |
| dc.citation.number | 11 | - |
| dc.citation.startPage | 1656 | - |
| dc.citation.endPage | 1662 | - |
| dc.identifier.bibliographicCitation | METABOLISM-CLINICAL AND EXPERIMENTAL, Vol.59(11) : 1656-1662, 2010 | - |
| dc.identifier.rimsid | 35138 | - |
| dc.type.rims | ART | - |
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