Article(id=1309634757877657931, tenantId=1146029695717560320, journalId=1227999776411738115, issueId=1309634747681304819, articleNumber=null, orderNo=null, doi=10.12048/j.issn.1674-229X.2026.01.009, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1737302400000, receivedDateStr=2025-01-20, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1790170858115, onlineDateStr=2026-09-23, pubDate=1769270400000, pubDateStr=2026-01-25, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1790170858115, onlineIssueDateStr=2026-09-23, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1790170858115, creator=13701087609, updateTime=1790170858115, updator=13701087609, issue=Issue{id=1309634747681304819, tenantId=1146029695717560320, journalId=1227999776411738115, year='2026', volume='36', issue='1', pageStart='1', pageEnd='80', issueExtLink='null', onlineDate='null', pubDate='1769270400000', pubDateStr='2026-01-25', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1790170855683, creator='13701087609', updateTime=1790219109143, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1309837137445482891, tenantId=1146029695717560320, journalId=1227999776411738115, issueId=1309634747681304819, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1309837137445482892, tenantId=1146029695717560320, journalId=1227999776411738115, issueId=1309634747681304819, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=49, endPage=52, ext={EN=ArticleExt(id=1309634758146093388, articleId=1309634757877657931, tenantId=1146029695717560320, journalId=1227999776411738115, language=EN, title=Relationship Between Serum Olanzapine Concentration and Metabolic Parameters in Patients: The Effect of Valproic Acid, columnId=null, journalTitle=Pharmacy Today, columnName=null, runingTitle=null, highlight=null, articleAbstract=
OBJECTIVE To investigate a potential relationship between metabolic parameters and steady-state serum concentration of olanzapine (OLA) in patients treated with OLA combined with or without VAL in patients with mental disorders.
METHODS A retrospective analysis was performed on 225 inpatients with mental disorders who received OLA monotherapy or OLA-VAL combination therapy. The serum concentration of OLA was measured, and fasting blood samples were analyzed for insulin, glucose, total cholesterol (TC), triglycerides (TG), high-density lipoprotein cholesterol (HDL-c), low-density lipoprotein cholesterol (LDL-c), and uric acid (UA). The effects of OLA serum concentration, with or without VAL, on the aforementioned parameters and the correlation with these parameters were investigated.
RESULTS VAL co-administration decreased OLA concentration and C/D ratio by 19.57% (P < 0.01) and 32.76%(P < 0.001), respectively.Patients taking OLA combined with VAL had higher weight (4.83%, P <0.01), BMI (4.07%, P < 0.05) and UA level (8.96%, P < 0.05), but lower glucose level (13.83%, P < 0.05), than those taking OLA alone. VAL co-administration had no significant effect on the levels of TC, HDL-c, LDL-c, TG and INS.The serum OLA concentration was negatively correlated with body weight in the OLA-VAL combination group (r =-0.199, P < 0.05), and there exists no correlation with other metabolic parameters.
CONCLUSION There is no correlation between the serum OLA concentration and glycolipid metabolic parameters in the OLA monotherapy group, however, a negative correlation is found between serum OLA concentration and body weight in the OLA-VAL combination group; meanwhile, significantly higher body weight, BMI and UA levels are observed in this group.
, authors=Shuhua DENG
1, Yongfeng LIU
2, Huanshan XIE
3, Jinqing HU
1, Chang QIU
1, Haoyang LU
1, Meixia LUO
1, Xiaojia NI
1, Dewei SHANG
1, Yuguan WEN
1, *, authorsList=Shuhua DENG, Yongfeng LIU, Huanshan XIE, Jinqing HU, Chang QIU, Haoyang LU, Meixia LUO, Xiaojia NI, Dewei SHANG, Yuguan WEN, authorCompany=null, correspAuthors=Yuguan WEN, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1309634758397751629, articleId=1309634757877657931, tenantId=1146029695717560320, journalId=1227999776411738115, language=CN, title=奥氮平血药浓度与精神障碍患者糖脂代谢指标的相关性研究:丙戊酸因素的影响, columnId=1228268588277105398, journalTitle=今日药学, columnName=临床药学, runingTitle=null, highlight=null, articleAbstract=
目的 探讨精神障碍患者联用与不联用丙戊酸(VAL)时,奥氮平(OLA)稳态血清浓度与糖脂代谢指标相关性。
方法 回顾性分析225例接受OLA或OLA合并VAL治疗的精神障碍住院患者。测定血清中OLA的浓度、空腹血中胰岛素(INS)、葡萄糖(GLU)、总胆固醇(TC)、甘油三酯(TG)、高密度脂蛋白胆固醇(HDL-c)、低密度脂蛋白胆固醇(LDL-c)及尿酸(UA)水平,探讨联用及不联用丙戊酸时,奥氮平浓度与上述代谢指标的相关性及对上述指标的影响。
结果 联用丙戊酸显著降低奥氮平浓度及C/D比值,分别降低19.57%(P < 0.01)及32.76%(P < 0.001),联用并丙戊酸显著增加患者体重、BMI及尿酸水平,分别为4.83%(P < 0.01)、4.07%(P < 0.05)及8.96%(P < 0.05),但空腹血糖水平偏低13.83%(P < 0.05),两组差异有统计学意义,奥氮平联用丙戊酸对TC、HDL-c、LDL-c、TG及INS水平无影响。联用丙戊酸组的奥氮平血药浓度与患者体重呈负相关,与其他指标不存在相关性。
结论 单独服用奥氮平浓度与患者糖脂代谢指标无相关性,但服用奥氮平联合丙戊酸的患者,其奥氮平浓度与体重存在负相关性,且体重及尿酸水平偏高。
, authors=邓书华
1, 刘永峰
2, 谢焕山
3, 胡晋卿
1, 邱畅
1, 卢浩扬
1, 罗美霞
1, 倪晓佳
1, 尚德为
1, 温预关
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