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The efficacy and safety of co-administration of fimasartan and rosuvastatin to patients with hypertension and dyslipidemia
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | 심지영 | - |
| dc.contributor.author | 윤영원 | - |
| dc.date.accessioned | 2017-11-02T08:07:43Z | - |
| dc.date.available | 2017-11-02T08:07:43Z | - |
| dc.date.issued | 2017 | - |
| dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/154111 | - |
| dc.description.abstract | BACKGROUND: Hypertension and dyslipidemia are major risk factors of cardiovascular disease (CVD) events. The objective of this study was to evaluate the efficacy and safety of the co-administration of fimasartan and rosuvastatin in patients with hypertension and hypercholesterolemia. METHODS: We conducted a randomized double-blind and parallel-group trial. Patients who met eligible criteria after 4 weeks of therapeutic life change were randomly assigned to the following groups. 1) co-administration of fimasartan 120 mg/rosuvastatin 20 mg (FMS/RSV), 2) fimasartan 120 mg (FMS) alone 3) rosuvastatin 20 mg (RSV) alone. Drugs were administered once daily for 8 weeks. RESULTS: Of 140 randomized patients, 135 for whom efficacy data were available were analyzed. After 8 weeks of treatment, the FMS/RSV treatment group showed greater reductions in sitting systolic (siSBP) and diastolic (siDBP) blood pressures than those in the group receiving RSV alone (both p < 0.001). Reductions in siSBP and siDBP were not significantly different between the FMS/RSV and FMS alone groups (p = 0.500 and p = 0.734, respectively). After 8 weeks of treatment, FMS/RSV treatment showed greater efficacy in percentage reduction of low-density lipoprotein cholesterol (LDL-C) level from baseline than that shown by FMS alone treatment (p < 0.001). The response rates of siSBP with FMS/RSV, FMS alone, and RSV alone treatments were 65.22, 55.56, and 34.09%, respectively (FMS/RSV vs. RSV, p = 0.006). The LDL-C goal attainment rates with FMS/RSV, RSV alone, and FMS alone treatments were 80.43%, 81.82%, and 15.56%, respectively (FMS/RSV vs. FMS, p < 0.001). Incidence of adverse drug reactions with FMS/RSV treatment was 8.33%, which was similar to those associated with FMS and RSV alone treatments. CONCLUSION: This study demonstrated that the co-administration of fimasartan and rosuvastatin to patients with both hypertension and hypercholesterolemia was efficacious and safe. | - |
| dc.description.statementOfResponsibility | open | - |
| dc.language | English | - |
| dc.publisher | BioMed Central | - |
| dc.relation.isPartOf | BMC PHARMACOLOGY & TOXICOLOGY | - |
| 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 | Aged | - |
| dc.subject.MESH | Angiotensin II Type 1 Receptor Blockers/administration & dosage | - |
| dc.subject.MESH | Angiotensin II Type 1 Receptor Blockers/adverse effects | - |
| dc.subject.MESH | Angiotensin II Type 1 Receptor Blockers/therapeutic use* | - |
| dc.subject.MESH | Anticholesteremic Agents/administration & dosage | - |
| dc.subject.MESH | Anticholesteremic Agents/adverse effects | - |
| dc.subject.MESH | Anticholesteremic Agents/therapeutic use* | - |
| dc.subject.MESH | Biphenyl Compounds/administration & dosage | - |
| dc.subject.MESH | Biphenyl Compounds/adverse effects | - |
| dc.subject.MESH | Biphenyl Compounds/therapeutic use* | - |
| dc.subject.MESH | Double-Blind Method | - |
| dc.subject.MESH | Drug Therapy, Combination | - |
| dc.subject.MESH | Female | - |
| dc.subject.MESH | Humans | - |
| dc.subject.MESH | Hypercholesterolemia/complications | - |
| dc.subject.MESH | Hypercholesterolemia/drug therapy* | - |
| dc.subject.MESH | Hypertension/complications | - |
| dc.subject.MESH | Hypertension/drug therapy* | - |
| dc.subject.MESH | Male | - |
| dc.subject.MESH | Middle Aged | - |
| dc.subject.MESH | Pyrimidines/administration & dosage | - |
| dc.subject.MESH | Pyrimidines/adverse effects | - |
| dc.subject.MESH | Pyrimidines/therapeutic use* | - |
| dc.subject.MESH | Rosuvastatin Calcium/administration & dosage | - |
| dc.subject.MESH | Rosuvastatin Calcium/adverse effects | - |
| dc.subject.MESH | Rosuvastatin Calcium/therapeutic use* | - |
| dc.subject.MESH | Tetrazoles/administration & dosage | - |
| dc.subject.MESH | Tetrazoles/adverse effects | - |
| dc.subject.MESH | Tetrazoles/therapeutic use* | - |
| dc.subject.MESH | Young Adult | - |
| dc.title | The efficacy and safety of co-administration of fimasartan and rosuvastatin to patients with hypertension and dyslipidemia | - |
| dc.type | Article | - |
| dc.publisher.location | England | - |
| dc.contributor.college | College of Medicine | - |
| dc.contributor.department | Dept. of Internal Medicine | - |
| dc.contributor.googleauthor | Moo-Yong Rhee | - |
| dc.contributor.googleauthor | Taehoon Ahn | - |
| dc.contributor.googleauthor | Kiyuk Chang | - |
| dc.contributor.googleauthor | Shung Chull Chae | - |
| dc.contributor.googleauthor | Tae-Hyun Yang | - |
| dc.contributor.googleauthor | Wan Joo Shim | - |
| dc.contributor.googleauthor | Tae Soo Kang | - |
| dc.contributor.googleauthor | Jae-Kean Ryu | - |
| dc.contributor.googleauthor | Deuk-Young Nah | - |
| dc.contributor.googleauthor | Tae-Ho Park | - |
| dc.contributor.googleauthor | In-Ho Chae | - |
| dc.contributor.googleauthor | Seung Woo Park | - |
| dc.contributor.googleauthor | Hae-Young Lee | - |
| dc.contributor.googleauthor | Seung-Jea Tahk | - |
| dc.contributor.googleauthor | Young Won Yoon | - |
| dc.contributor.googleauthor | Chi Young Shim | - |
| dc.contributor.googleauthor | Dong-Gu Shin | - |
| dc.contributor.googleauthor | Hong Seog Seo | - |
| dc.contributor.googleauthor | Sung Yun Lee | - |
| dc.contributor.googleauthor | Doo Il Kim | - |
| dc.contributor.googleauthor | Jun Kwan | - |
| dc.contributor.googleauthor | Seung-Jae Joo | - |
| dc.contributor.googleauthor | Myung Ho Jeong | - |
| dc.contributor.googleauthor | Jin-Ok Jeong | - |
| dc.contributor.googleauthor | Ki Chul Sung | - |
| dc.contributor.googleauthor | Seok Yeon Kim | - |
| dc.contributor.googleauthor | Sang-Hyun Kim | - |
| dc.contributor.googleauthor | Kook-Jin Chun | - |
| dc.contributor.googleauthor | Dong Joo Oh | - |
| dc.identifier.doi | 10.1186/s40360-016-0112-7 | - |
| dc.contributor.localId | A02580 | - |
| dc.contributor.localId | A02213 | - |
| dc.relation.journalcode | J03069 | - |
| dc.identifier.eissn | 2050-6511 | - |
| dc.relation.journalsince | 2012 | - |
| dc.identifier.pmid | 28057081 | - |
| dc.subject.keyword | Fimasartan | - |
| dc.subject.keyword | Hypercholesterolemia | - |
| dc.subject.keyword | Hypertension | - |
| dc.subject.keyword | Rosuvastatin | - |
| dc.contributor.alternativeName | Shim, Chi Young | - |
| dc.contributor.alternativeName | Yoon, Young Won | - |
| dc.contributor.affiliatedAuthor | Yoon, Young Won | - |
| dc.contributor.affiliatedAuthor | Shim, Chi Young | - |
| dc.citation.title | BMC Pharmacology & Toxicology | - |
| dc.citation.volume | 18 | - |
| dc.citation.number | 2 | - |
| dc.citation.startPage | 1 | - |
| dc.citation.endPage | 11 | - |
| dc.identifier.bibliographicCitation | BMC PHARMACOLOGY & TOXICOLOGY, Vol.18(2) : 1-11, 2017 | - |
| dc.date.modified | 2017-11-01 | - |
| dc.identifier.rimsid | 41606 | - |
| dc.type.rims | ART | - |
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