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Search: L773:0891 5849 OR L773:1873 4596 > Urinary excretion o...

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00003554naa a2200313 4500
001oai:DiVA.org:liu-23882
003SwePub
008091007s2004 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-238822 URI
024a https://doi.org/10.1016/j.freeradbiomed.2003.11.0222 DOI
040 a (SwePub)liu
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Bergman, Vivi4 aut
2451 0a Urinary excretion of 8-hydroxydeoxyguanosine and malondialdehyde after high dose radiochemotherapy preceding stem cell transplantation
264 1b Elsevier BV,c 2004
338 a print2 rdacarrier
520 a The urinary excretion of the hydroxylated DNA base 8-hydroxydeoxyguanosine (8-OHdG) and the lipid peroxidation product malondialdehyde (MDA) was monitored in 11 patients with hematological malignancies undergoing total body irradiation and high-dose chemotherapy preceding bone marrow transplantation. Nine patients showed a prompt increase in urinary 8-OHdG (8-25 times the initial baseline level) on days 0-7 after irradiation onset, the excretion then decreased during the aplastic period and increased again when engraftment took place (in 7 patients). A significant positive correlation was found between urinary 8-OHdG and whole blood leukocyte count, both on day 5 (p = .04, r = .72) and on day 22 (p = .009, r = .80) after irradiation onset. One patient who lacked the first peak of 8-OHdG excretion showed low blood leukocyte counts (less than 2×109/l) before therapy onset, this patient, however, later had a successful engraftment and then also showed considerable increases in both 8-OHdG excretion and leukocyte count. These observations suggest leukocytes play a part in the excretion of 8-OHdG after conditioning therapy preceding bone marrow transplantation. As opposed to the biphasic 8-OHdG excretion, the excretion of MDA showed a single peak appearing on days 11-19 after radiochemotherapy onset, i.e., during the period in which the patients suffered from cytopenia, mucositis, and other side effects of the treatment. It is suggested, therefore, that these clinical manifestations are associated with increased lipid peroxidation. Altogether, these findings illustrate the utility of serial urinary samples for monitoring oxidative stress due to conditioning therapy in clinical practice. They also demonstrate that different oxidative stress markers may behave quite differently regarding their appearance in the urine after whole-body oxidative stress.
653 a MEDICINE
653 a MEDICIN
700a Leanderson, Per,d 1958-u Östergötlands Läns Landsting,Linköpings universitet,Hälsouniversitetet,Yrkes- och miljömedicin,Yrkes- och miljömedicinskt centrum4 aut0 (Swepub:liu)perle80
700a Starkhammar, Hans,d 1948-u Östergötlands Läns Landsting,Linköpings universitet,Hälsouniversitetet,Onkologi,Onkologiska kliniken US4 aut0 (Swepub:liu)hanst87
700a Tagesson, Christer,d 1948-u Östergötlands Läns Landsting,Linköpings universitet,Hälsouniversitetet,Yrkes- och miljömedicin,Yrkes- och miljömedicinskt centrum4 aut0 (Swepub:liu)chrta55
710a Linköpings universitetb Hälsouniversitetet4 org
773t Free Radical Biology & Medicined : Elsevier BVg 36:3, s. 300-306q 36:3<300-306x 0891-5849x 1873-4596
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-23882
8564 8u https://doi.org/10.1016/j.freeradbiomed.2003.11.022

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