PDI
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Perit Dial Int 22(1): 48-52 2002
© 2002 International Society for Peritoneal Dialysis
This Article
Right arrow Full Text (PDF)
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Capodicasa, E
Right arrow Articles by Buoncristiani, U
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Capodicasa, E
Right arrow Articles by Buoncristiani, U
Peritoneal Dialysis International, Vol 22, Issue 1, 48-52
Copyright © 2002 by International Society for Peritoneal Dialysis


Evaluation Studies

Lack of isoprene overproduction during peritoneal dialysis

E Capodicasa, G Trovarelli, F Brunori, L Vecchi, C Carobi, M De, MA Pelli, and U Buoncristiani

Department of Clinical and Experimental Medicine, Perugia University Medical School, Italy. encap@unipg.it

OBJECTIVE: Isoprene is the constitutive unit of isoprenoid lipids and sterols. However, it is also a potential toxic and carcinogenic agent. Recent findings of a marked and prolonged isoprene overproduction induced by hemodialysis sessions raises the question of isoprene behavior in patients on peritoneal dialysis. DESIGN: A study with repeated measures per patient and healthy control. SETTING: Nephrology and Dialysis Unit and Perugia University Medical School. PATIENTS: Sixteen consecutive patients on regular continuous ambulatory peritoneal dialysis (CAPD) were evaluated. Endogenous isoprene was analyzed using gas chromatographic assay of breath isoprene, collected at set times before and after dialysis fluid exchange. RESULTS: No significant variations were found in breath isoprene concentrations in the different samples from each patient, and levels were almost stable within the normal range of healthy controls. CONCLUSION: These results show that CAPD, unlike hemodialysis, has little or no effect on isoprene and isoprenoid-related lipid turnover. This lack of increased endogenous isoprene synthesis, in addition to being a distinctive metabolic feature of CAPD, could have important pathophysiological and clinical implications.




This article has been cited by other articles:


Home page
Nephrol Dial TransplantHome page
P. Lirk, F. Bodrogi, H. Raifer, K. Greiner, H. Ulmer, and J. Rieder
Elective haemodialysis increases exhaled isoprene
Nephrol. Dial. Transplant., May 1, 2003; 18(5): 937 - 941.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Multimed Inc. logo
Copyright © 2002 by Multimed Inc.