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1.
Kidney Int ; 70(10): 1823-31, 2006 Nov.
Article in English | MEDLINE | ID: mdl-17003818

ABSTRACT

Although the association of angiotensin I-converting enzyme inhibitors (ACEis) with a negatively charged membrane is thought to be responsible for hypersensitivity reactions (HSRs) during hemodialysis, we hypothesize that these complications are due to changes in plasma aminopeptidase P (APP) activity and genotype. To test this hypothesis, we measured plasma APP activity in 14 patients who suffered HSR (HSR+) while dialyzed with an AN69 membrane and simultaneously treated with an ACEi. APP activity was also studied in a control group (n=39) dialyzed under the same conditions, but who did not suffer any side effect (HSR-). We found significantly decreased plasma APP activity (P=0.013) in HSR+ subjects as well as altered degradation of endogenous des-Arginine(9)-bradykinin, with a significantly lower beta value (P<0.001). The same analytical approach was taken in 171 relatives of HSR+ patients. Variance component analysis suggested that genetic differences may explain 61% of the phenotypic variability of plasma APP activity (P<0.001) and the kinetic parameters that characterized kinin degradation. We also showed that the C-2399A single-nucleotide polymorphism at the XPNPEP2 locus was a significant predictor of APP activity in the 39 HSR- controls (P=0.029). Furthermore, a recessive genetic model for the A allele disclosed a significant difference in mean APP activity by genotype (P<0.001). Finally, our study defined the nonspecific inhibition of recombinant APP by some ACEis. In conclusion, this paper highlights the complexity of HSR in hemodialysis, suggesting, as with angioedema, that these rare, but life-threatening adverse events are governed by several metabolic and genetic factors.


Subject(s)
Aminopeptidases/metabolism , Angiotensin-Converting Enzyme Inhibitors/adverse effects , Drug Hypersensitivity/etiology , Drug Hypersensitivity/metabolism , Kinins/metabolism , Renal Dialysis/adverse effects , Adult , Aged , Aminopeptidases/genetics , Bradykinin/analogs & derivatives , Bradykinin/genetics , Bradykinin/metabolism , Cohort Studies , Drug Hypersensitivity/genetics , Female , Genetic Linkage/genetics , Humans , Kinins/genetics , Male , Middle Aged , Pedigree , Polymorphism, Single Nucleotide , Renal Dialysis/methods
2.
Ann Pharm Fr ; 64(4): 276-86, 2006 Jul.
Article in French | MEDLINE | ID: mdl-16902391

ABSTRACT

Angiotensin converting enzyme inhibitors are a class of drugs successfully used in the treatment of cardiovascular diseases. Despite their effectiveness, treatment with these drugs is characterized by chronic and acute side effects with variable expression depending on the clinical context. Angioedema occurs in patients with hypertension or heart failure. Anaphylactoid reaction is also reported in hemodialysis patients and severe hypotensive reaction in patients receiving transfused blood products and plasmapheresis. In this paper, we describe the role of kinins and metallopeptidases in the pathophysiology of these acute side effects. We also propose different experimental and clinical evidences which plead for an ecogenetic nature of these rare but life-threatening events.


Subject(s)
Angiotensin-Converting Enzyme Inhibitors/adverse effects , Acute Disease , Animals , Humans , Kallikrein-Kinin System/physiology
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