|
|
Effect of erythropoietin-stimulating agent on uremic inflammation
|
|
|
|
|
نویسنده
|
tanaka y. ,joki n. ,hase h. ,iwasaki m. ,ikeda m. ,ando r. ,shinoda t. ,inaguma d. ,sakaguchi t. ,komatsu y. ,koiwa f. ,yamaka t. ,shigematsu t.
|
منبع
|
journal of inflammation - 2012 - دوره : 9 - شماره : 0
|
چکیده
|
Background: the goal of the present study was to explore the effect of medications that are commonly prescribed for ckd patients on uremic state. methods: this was a cross-sectional study. from january 2006 to october 2009,1,623 patients with end-stage kidney disease (eskd) commenced hemodialysis (hd) at the 9 participating hospitals. the criteria for exclusion from the database were 1) serum c-reactive protein (crp) >3 mg/dl,2) wbc count >9,000/mm3 or <4,000/mm3,and 3) patients with cancer,immune complex disease,or vasculitis. a total of 900 patients were entered into the final database. we explored the association of serum crp just before the first hd session with clinical characteristics,laboratory data,and medications for ckd in the predialysis period. results: on univariate analysis,age,ctr,egfr,and wbc were significantly correlated with crp. systolic and diastolic blood pressure,serum albumin,ldl-c,hdl-c,hb,cr,and ca were inversely associated with crp. use of erythropoietin-stimulating agents (esa) using (r = ?0.111,p = 0.0015),renin-angiotensin-aldosterone system inhibitors (r = ?0.083,p = 0.0154),and calcium channel blockers (r = ?0.1,p = 0.0039) was also negatively correlated with crp. however,only use of esa showed a significant negative correlation with crp that was independent of other clinical factors and ckd medications on multiple regression analysis. conclusion: esa may strongly reduce uremic inflammation in addition to improving anemia. to confirm this potential effect,a large-scale longitudinal study would be required. © 2012 tanaka et al.; licensee biomed central ltd.
|
کلیدواژه
|
ACE-I/ARB; CRP; Erythropoietin stimulating agent; Inflammation; Initiation of dialysis
|
آدرس
|
division of nephrology,toho university ohashi medical center,2-17-6,ohashi,tokyo,meguro-ku,153-8515, Japan, division of nephrology,toho university ohashi medical center,2-17-6,ohashi,tokyo,meguro-ku,153-8515, Japan, division of nephrology,toho university ohashi medical center,2-17-6,ohashi,tokyo,meguro-ku,153-8515, Japan, division of nephrology,toho university ohashi medical center,2-17-6,ohashi,tokyo,meguro-ku,153-8515, Japan, department of medicine,aoto general hospital,jikei university school of medicine,tokyo, Japan, department of nephrology,musashino red cross hospital,tokyo, Japan, dialysis center,kawakita general hospital,tokyo, Japan, kidney center,nagoya daini red cross hospital,nagoya, Japan, division of nephrology and blood purification medicine,wakayama medical university,wakayama, Japan, department of nephrology,division of internal medicine,st. lukes international hospital,tokyo, Japan, division of nephrology,department of internal medicine,showa university fujigaoka hospital,yokohama, Japan, department of clinical engineering,social insurance chuo general hospital,tokyo, Japan, department of nephrology,division of internal medicine,st. lukes international hospital,tokyo, Japan
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Authors
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|