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résumés des cours et travaux - Collège de France

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RÉSUMÉS DES COURS ET CONFÉRENCES 931<br />

therapy, giving rise to the feeling that these agents have beneficial effects above and<br />

beyond what can be achieved with blood pressure control alone.<br />

At present, there is a balancing act b<strong>et</strong>ween the control of blood pressure and<br />

control of proteinuria. Even in the most well <strong>de</strong>fined outcome studies of type I,<br />

and type II diab<strong>et</strong>es, the outcomes with respect to slowing the rate of progression<br />

of CKD, though significant, do not achieve the ultimate goal of reducing the<br />

progression rate to < 1 ml/min/1.73 m 2 /year.<br />

A new paradigm is emerging that focuses directly on the control of proteinuria to<br />

less than 0.5 grams/day with ACEI/ARB therapy and also other non-traditional<br />

forms of therapy including other forms of RAS blockers, vitamin D, and other<br />

agents.<br />

These issues will be put in focus for the case of Fabry nephropathy. Fabry disease<br />

is a rate multi-system disease caused by a mutation in the alpha-galactosidase A<br />

gene on the X-chromosome. It is a progressive form of proteinuric CKD, but in<br />

contrast to diab<strong>et</strong>es, the systolic blood pressure is not usually elevated, which<br />

makes the utilization of traditional anti-proteinuric therapy challenging.<br />

In conclusion, the importance of control of proteinuria in slowing the progression<br />

of CKD will be emphasized with the use of a combination of treatment approaches<br />

to achieve this goal. In this context, control of proteinuria, per se, rather than<br />

lowering the systolic blood pressure to an arbitrary, fixed goal becomes the primary<br />

outcome measure. While this approach clearly has merit, long-term outcome<br />

studies are need before reduction of urinary protein excr<strong>et</strong>ion can be accepted as<br />

a surrogate endpoint for slowing the progression of CKD.

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