The PROPKD Score: A New Algorithm to Predict Renal Survival in Autosomal Dominant Polycystic Kidney Disease

被引:256
作者
Cornec-Le Gall, Emilie [1 ,2 ,3 ]
Audrezet, Marie-Pierre [3 ,4 ]
Rousseau, Annick [5 ]
Hourmant, Maryvonne [6 ]
Renaudineau, Eric [7 ]
Charasse, Christophe [8 ]
Morin, Marie-Pascale [9 ]
Moal, Marie-Christine [1 ]
Dantal, Jacques [6 ]
Wehbe, Batsenn [10 ]
Perrichot, Regine [11 ]
Frouget, Thierry [9 ]
Vigneau, Cecile [9 ]
Potier, Jerome [8 ]
Jousset, Philippe [12 ]
Guillodo, Marie-Paule [13 ]
Siohan, Pascale [10 ]
Terki, Nazim [14 ]
Sawadogo, Theophile [15 ]
Legrand, Didier [16 ]
Menoyo-Calonge, Vittorio [17 ]
Benarbia, Saddik [18 ]
Besnier, Dominique [19 ]
Longuet, Helene [20 ]
Ferec, Claude [2 ,3 ,4 ,21 ]
Le Meur, Yannick [1 ,2 ]
机构
[1] Univ Hosp, Dept Nephrol, Brest, France
[2] European Univ Brittany, Brest, France
[3] INSERM, Natl Inst Hlth & Med Sci, U01078, Brest, France
[4] Univ Hosp, Dept Mol Genet, Brest, France
[5] Univ Hosp, INSERM, Dept Pharmacol, U850, Limoges, France
[6] Univ Hosp, Dept Nephrol, Nantes, France
[7] Hop Broussais, Dept Nephrol, St Malo, France
[8] Yves Le Foll Hosp, Dept Nephrol, St Brieuc, France
[9] Univ Hosp, Dept Nephrol, Rennes, France
[10] Laenneck Hosp, Dept Nephrol, Quimper, France
[11] Vannes Hosp, Dept Nephrol, Vannes, France
[12] Pontivy Hosp, Dept Nephrol, Pontivy, France
[13] AUB Sante, Brest, France
[14] SBRA, Hemodialysis Unit, Brest, France
[15] Lorient Hosp, Dept Nephrol, Lorient, France
[16] AUB Sante, Lorient, France
[17] ECHO Dialysis Unit, Vannes, France
[18] AUB Sante, Quimper, France
[19] St Nazaire Hosp, Dept Nephrol, St Nazaire, France
[20] Univ Hosp, Dept Nephrol, Tours, France
[21] EFS Bretagne, Brest, France
来源
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2016年 / 27卷 / 03期
关键词
IDENTIFICATION; GROWTH; VOLUME; PKD1;
D O I
10.1681/ASN.2015010016
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
The course of autosomal dominant polycystic kidney disease (ADPKD) varies among individuals, with some reaching ESRD before 40 years of age and others never requiring RRT. In this study, we developed a prognostic model to predict renal outcomes in patients with ADPKD on the basis of genetic and clinical data. We conducted a cross-sectional study of 1341 patients from the Genkyst cohort and evaluated the influence of clinical and genetic factors on renal survival. Multivariate survival analysis identified four variables that were significantly associated with age at ESRD onset, and a scoring system from 0 to 9 was developed as follows: being male: 1 point; hypertension before 35 years of age: 2 points; first urologic event before 35 years of age: 2 points; PKD2 mutation: 0 points; nontruncating PKD1 mutation: 2 points; and truncating PKD1 mutation: 4 points. Three risk categories were subsequently defined as low risk (0-3 points), intermediate risk (4-6 points), and high risk (7-9 points) of progression to ESRD, with corresponding median ages for ESRD onset of 70.6, 56.9, and 49 years, respectively. Whereas a score <= 3 eliminates evolution to ESRD before 60 years of age with a negative predictive value of 81.4%, a score >6 forecasts ESRD onset before 60 years of age with a positive predictive value of 90.9%. This new prognostic score accurately predicts renal outcomes In patients with ADPKD and may enable the personalization of therapeutic management of ADPKD.
引用
收藏
页码:942 / 951
页数:10
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