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Effect of organic solvent exposure on chronic kidney disease progression: the GN-PROGRESS cohort study.
Jacob S., Héry M., Protois J.-C., Rossert J., Stengel B.
J Am Soc Nephrol 18, 1 (2007) 274-81 - http://www.hal.inserm.fr/inserm-00134002
(17135394)
Effect of organic solvent exposure on chronic kidney disease progression: the GN-PROGRESS cohort study.
Sophie Jacob () 1, Michel Héry2, Jean-Claude Protois2, Jérôme Rossert3, 4, Bénédicte Stengel1
1:  Recherche en épidémiologie et biostatistique
INSERM : IFR69 – Université Paris XI - Paris Sud
16, Avenue Paul Vaillant-Couturier 94807 VILLEJUIF CEDEX
France
2:  Institut National de Recherche et de Sécurité
INRS
Vandoeuvre-les-Nancy
France
3:  Physiologie et pharmacologie vasculaire et rénale
INSERM : U652 – IFR58 – Université Paris V - Paris Descartes
Institut Biomedical Des Cordeliers 15, Rue de L'Ecole de Medecine 75270 Paris Cedex 06
France
4:  Service de néphrologie
Assistance publique - Hôpitaux de Paris (AP-HP) – Hôpital européen Georges Pompidou – Université Paris V - Paris Descartes
Paris
France
Solvent Exposure and Kidney Disease Progression
It has been suggested that solvent exposure may have a role in the progression of glomerulonephritis (GN) to ESRD, but this has never been tested with an appropriate cohort study design. A total of 338 non-ESRD patients with a first biopsy for primary GN between 1994 and 2001 were included: 194 IgA nephropathies (IgAN), 75 membranous nephropathies (MN), and 69 FSGS. ESRD, defined as an estimated GFR <15 ml/min per 1.73 m2 or dialysis, was registered during a mean follow-up period of 5 yr. Patients' lifelong solvent exposures before and after diagnosis were recorded by interview and assessed by industrial hygienist experts. Cox models were used to estimate adjusted hazard ratios (HR) of ESRD related to exposures. Overall, 15 and 14% of the patients had been exposed at a low and a high level before diagnosis, respectively. Forty-two with IgAN, 12 with MN, and 22 with FSGS reached ESRD. A graded relationship was observed for MN (age- and gender-adjusted HR [95% confidence interval] for low exposure versus none was 3.1 [0.5 to 18.2] and for high exposure versus none was 8.2 [1.9 to 34.7]) and for IgAN (1.6 [0.7 to 3.9] and 2.2 [1.0 to 4.8]) but not for FSGS. Solvent risk was mediated only partly by baseline proteinuria: Adjusted HR for high exposure versus none was 5.5 (1.3 to 23.9) for MN and 1.8 (0.8 to 3.9) for IgAN. In patients with IgAN, there was a trend in increasing HR with exposure duration before and its persistence after diagnosis. These findings support the hypothesized association of solvent exposure with the progression of GN to ESRD. They should prompt clinicians to give greater attention to patients' occupational exposures and possibly to consider professional reclassification.
Life Sciences/Health Care Sciences and Epidemiology
Life Sciences/Toxicology
English
1046-6673

Article in peer-reviewed journal
10.1681/ASN.2006060652
J Am Soc Nephrol
2007-01
2006-11-29
18
1
274-81

Organic solvents – glomerulonephritis – membranous nephropathy – IgA nephropathy – focal and segmental glomerulosclerosis – end stage renal disease – environmental exposure
Ministère de la Santé (PHRC AOM 00022) Ministère de l'Environnement (Décision d'aide EN00D08) Ministère de la Recherche (Décision d'aide 01P0513) Agence de Biomédecine (AO Recherche et Greffes 2005) Agence de l'Environnement et de la Maitrise de l'Energie - ADEME (Bourse de thèse)