Tolvaptan and Kidney Pain in Patients With Autosomal Dominant Polycystic Kidney Disease: Secondary Analysis From a Randomized Controlled Trial

被引:34
作者
Casteleijn, Niek F. [1 ]
Blais, Jaime D. [2 ]
Chapman, Arlene B. [3 ]
Czerwiec, Frank S. [2 ]
Devuyst, Olivier [4 ]
Higashihara, Eiji [5 ]
Leliveld, Anna M. [6 ]
Ouyang, John [2 ]
Perrone, Ronald D. [7 ]
Torres, Vicente E. [8 ]
Gansevoort, Ron T. [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Nephrol, Groningen, Netherlands
[2] Otsuka Pharmaceut Dev & Commercializat Inc, Rockville, MD USA
[3] Emory Univ, Sch Med, Div Nephrol, Atlanta, GA USA
[4] Univ Zurich, Inst Physiol, Zurich Ctr Integrat Human Physiol, Zurich, Switzerland
[5] Kyorin Univ, Dept Urol, Sch Med, Mitaka, Tokyo, Japan
[6] Univ Groningen, Univ Med Ctr Groningen, Dept Urol, Groningen, Netherlands
[7] Tufts Univ, Sch Med, Div Nephrol, Tufts Med Ctr, Boston, MA 02111 USA
[8] Mayo Clin, Div Nephrol & Hypertens, Dept Internal Med, Rochester, MN USA
关键词
Autosomal dominant polycystic kidney disease (ADPKD); pain; tolvaptan; vasopressin; acute kidney pain event; TEMPO (Tolvaptan Efficacy and Safety in Management of Autosomal Dominant Polycystic Kidney Disease and Its Outcomes) 3:4; pain severity; analgesic; QUALITY-OF-LIFE; VASOPRESSIN; MANAGEMENT; FAILURE;
D O I
10.1053/j.ajkd.2016.08.028
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: Kidney pain is a common complication in patients with autosomal dominant polycystic kidney disease (ADPKD), and data from the TEMPO 3: 4 trial suggested that tolvaptan, a vasopressin V2 receptor antagonist, may have a positive effect on kidney pain in this patient group. Because pain is difficult to measure, the incidence of kidney pain leading to objective medical interventions was used in the present study to assess pain. Study Design: Secondary analysis from a randomized controlled trial. Setting & Participants: Patients with ADPKD with preserved kidney function. Intervention: Tolvaptan or placebo. Outcomes: Kidney pain events defined by objective medical interventions. Measurements: Kidney pain events were recorded and independently adjudicated. Incidence of a first kidney pain event was assessed overall and categorized into 5 subgroups according to severity. Results: Of 1,445 participating patients (48.4% women; mean age, 39 +/- 7 [SD] years; mean estimated glomerular filtration rate, 81 +/- 22 mL/min/1.73 m(2); median total kidney volume, 1,692 [IQR, 750-7,555] mL), 50.9% reported a history of kidney pain at baseline. History of urinary tract infections, kidney stones, or hematuria (all P < 0.001) and female sex (P < 0.001) were significantly associated with history of kidney pain. Tolvaptan use resulted in a significantly lower incidence of kidney pain events when compared to placebo: 10.1% versus 16.8% (P < 0.001), with a risk reduction of 36% (HR, 0.64; 95% CI, 0.48-0.86). The reduction in pain event incidence by tolvaptan was found in all groups irrespective of pain severity and was independent of predisposing factors (P for interaction > 0.05). The effect of tolvaptan was explained at least in part by a decrease in incidence of urinary tract infections, kidney stones, and hematuria when compared to placebo. Limitations: Trial has specific inclusion criteria for total kidney volume and kidney function. Conclusions: Tolvaptan decreased the incidence of kidney pain events independent of patient characteristics predisposing for kidney pain and possibly in part due to reductions in ADPKD-related complications. (C) 2016 The Authors. Published by Elsevier Inc. on behalf of the National Kidney Foundation, Inc.
引用
收藏
页码:210 / 219
页数:10
相关论文
共 21 条
[1]  
[Anonymous], AM J KIDNEY DIS
[2]   Pain patterns in patients with polycystic kidney disease [J].
Bajwa, ZH ;
Sial, KA ;
Malik, AB ;
Steinman, TI .
KIDNEY INTERNATIONAL, 2004, 66 (04) :1561-1569
[3]   Pain management in polycystic kidney disease [J].
Bajwa, ZH ;
Gupta, S ;
Warfield, CA ;
Steinman, TI .
KIDNEY INTERNATIONAL, 2001, 60 (05) :1631-1644
[4]   Sex differences in pain: a brief review of clinical and experimental findings [J].
Bartley, E. J. ;
Fillingim, R. B. .
BRITISH JOURNAL OF ANAESTHESIA, 2013, 111 (01) :52-58
[5]   Short-term renal hemodynamic effects of tolvaptan in subjects with autosomal dominant polycystic kidney disease at various stages of chronic kidney disease [J].
Boertien, Wendy E. ;
Meijer, Esther ;
de Jong, Paul E. ;
Bakker, Stephan J. L. ;
Czerwiec, Frank S. ;
Struck, Joachim ;
Oberdhan, Dorothee ;
Shoaf, Susan E. ;
Krasa, Holly B. ;
Gansevoort, Ron T. .
KIDNEY INTERNATIONAL, 2013, 84 (06) :1278-1286
[6]   A stepwise approach for effective management of chronic pain in autosomal-dominant polycystic kidney disease [J].
Casteleijn, Niek F. ;
Visser, Folkert W. ;
Drenth, Joost P. H. ;
Gevers, Tom J. G. ;
Groen, Gerbrand J. ;
Hogan, Marie C. ;
Gansevoort, Ron T. .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2014, 29 :142-153
[7]   AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE [J].
GABOW, PA .
NEW ENGLAND JOURNAL OF MEDICINE, 1993, 329 (05) :332-342
[8]  
Hogan Marie C, 2010, Adv Chronic Kidney Dis, V17, pe1, DOI 10.1053/j.ackd.2010.01.005
[9]   PROTEIN-KINASE-C ACTIVATORS STIMULATE BETA-ENDORPHIN SECRETION FROM HYPOTHALAMIC CELLS [J].
KAPCALA, LP ;
WENG, CF ;
JUANG, HH .
BRAIN RESEARCH BULLETIN, 1992, 29 (05) :553-557
[10]   New Topics in Vasopressin Receptors and Approach to Novel Drugs: Vasopressin and Pain Perception [J].
Koshimizu, Taka-aki ;
Tsujimoto, Gozoh .
JOURNAL OF PHARMACOLOGICAL SCIENCES, 2009, 109 (01) :33-37