Hyperhomocysteinemia and changed plasma thiol redox status in chronic obstructive pulmonary disease

Anders Andersson, Jaro Ankerst, Arne Lindgren, Kerstin Larsson, Björn Hultberg

Research output: Contribution to journalArticlepeer-review

Abstract

Reduced and total homocysteine, cysteine, glutathione and cysteinylglycine in plasma were investigated in 19 patients with chronic obstructive pulmonary disease and in 29 healthy subjects. The purpose was to examine the influence of pro-oxidant activity caused by the lung disease on the metabolism of homocysteine and other plasma thiols. We observed a decreased concentration of reduced glutathione and a decreased ratio of reduced/total glutathione in the patients compared to the healthy individuals, which supports the hypothesis of an association between free radicals and pathogenesis in some lung diseases. We also observed an increased total plasma homocysteine. The influence of a possible extracellular pro-oxidant activity on the concentration of total plasma homocysteine is discussed.
Original languageEnglish
Pages (from-to)229-233
JournalClinical Chemistry and Laboratory Medicine
Volume39
Issue number3
Publication statusPublished - 2001

Subject classification (UKÄ)

  • Clinical Laboratory Medicine

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