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Rapid Decrease of Intact Parathyroid Hormone Could Be a Predictor of Better Response to Cinacalcet in Hemodialysis Patients

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dc.contributor.authorKim, Jwa-Kyung-
dc.contributor.authorKwon, Young Joo-
dc.contributor.authorKim, Soo Wan-
dc.contributor.authorKim, Yeong-Hoon-
dc.contributor.authorPark, Cheol Whee-
dc.contributor.authorChoi, Kyu Bok-
dc.contributor.authorHwang, Seung Duk-
dc.contributor.authorChoi, Kyu Hun-
dc.date.accessioned2021-09-06T03:41:33Z-
dc.date.available2021-09-06T03:41:33Z-
dc.date.created2021-06-14-
dc.date.issued2013-03-01-
dc.identifier.issn0513-5796-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/103763-
dc.description.abstractPurpose: Cinacalcet is effective for treating refractory secondary hyperparathyroidism (SHPT), but little is known about the response rates and clinical factors influencing the response. Materials and Methods: A prospective, single-arm, multi-center study was performed for 24 weeks. Cinacalcet was administered to patients with intact parathyroid hormone (iPTH) level greater than 300 pg/mL. Cinacalcet was started at a dose of 25 mg daily and titrated until 100 mg to achieve a serum iPTH level <300 pg/mL (primary end point). Early response to cinacalcet was defined as a decrease of iPTH more than 50% within one month. Results: Fifty-seven patients were examined. Based on the magnitude of iPTH decrease, patients were divided into responder (n=47, 82.5%) and non-responder (n=10, 17.5%) groups. Among the responders, 38 achieved the primary end point, whereas 9 patients showed a reduction in serum iPTH of 30% or more, but did not reach the primary end point. Compared to non-responders, responders were significantly older (p=0.026), female (p=0.041), and diabetics (p<0.001). Additionally, early response was observed more frequently in the responders (30/47, 63.8%), of whom the majority (27/30, 90.0%) achieved the primary end point. Multivariate analysis showed that lower baseline iPTH levels [odds ratio (OR) 0.96, 95% confidence interval (CI) 0.93-0.99], the presence of diabetes (OR 46.45, CI 1.92-1125.6) and early response (OR 21.54, CI 2.94-157.7) were significant clinical factors affecting achievement of iPTH target. Conclusion: Cinacalcet was effective in most hemodialysis patients with refractory SHPT. The presence of an early response was closely associated with the achievement of target levels of iPTH.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherYONSEI UNIV COLL MEDICINE-
dc.subjectSECONDARY HYPERPARATHYROIDISM-
dc.subjectCALCIMIMETIC AGENT-
dc.subjectBONE METABOLISM-
dc.subjectSERUM-CALCIUM-
dc.subjectDIALYSIS-
dc.subjectDISEASE-
dc.subjectOUTCOMES-
dc.subjectHCL-
dc.subjectPTH-
dc.titleRapid Decrease of Intact Parathyroid Hormone Could Be a Predictor of Better Response to Cinacalcet in Hemodialysis Patients-
dc.typeArticle-
dc.contributor.affiliatedAuthorKwon, Young Joo-
dc.identifier.doi10.3349/ymj.2013.54.2.453-
dc.identifier.scopusid2-s2.0-84873272867-
dc.identifier.wosid000315540600026-
dc.identifier.bibliographicCitationYONSEI MEDICAL JOURNAL, v.54, no.2, pp.453 - 463-
dc.relation.isPartOfYONSEI MEDICAL JOURNAL-
dc.citation.titleYONSEI MEDICAL JOURNAL-
dc.citation.volume54-
dc.citation.number2-
dc.citation.startPage453-
dc.citation.endPage463-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.identifier.kciidART001745374-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaGeneral & Internal Medicine-
dc.relation.journalWebOfScienceCategoryMedicine, General & Internal-
dc.subject.keywordPlusSECONDARY HYPERPARATHYROIDISM-
dc.subject.keywordPlusCALCIMIMETIC AGENT-
dc.subject.keywordPlusBONE METABOLISM-
dc.subject.keywordPlusSERUM-CALCIUM-
dc.subject.keywordPlusDIALYSIS-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordPlusOUTCOMES-
dc.subject.keywordPlusHCL-
dc.subject.keywordPlusPTH-
dc.subject.keywordAuthorCinacalcet-
dc.subject.keywordAuthorend-stage renal disease-
dc.subject.keywordAuthorhemodialysis-
dc.subject.keywordAuthorparathyroid hormone-
dc.subject.keywordAuthorsecondary hyperparathyroidism-
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