2008
DOI: 10.1016/s0016-5085(08)62303-3
|View full text |Cite
|
Sign up to set email alerts
|

T1144 Results of a Long-Term Follow-Up Treatment with Delayed Release Phosphatidylcholine in Chronic-Active Ulcerative Colitis

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

0
3
0

Year Published

2010
2010
2017
2017

Publication Types

Select...
5

Relationship

1
4

Authors

Journals

citations
Cited by 5 publications
(3 citation statements)
references
References 0 publications
0
3
0
Order By: Relevance
“…In addition, phospholipase A2 (PLA2) that catalyzes the degradation of PC to lysoPC [52], showed elevated content and activity in animal models of colitis and in actively inflamed colonic mucosa of UC patients compared to the inactively inflamed mucosa and the control [53][54][55][56]. The upregulation of PLA2 is consistent with the higher lysoPC-to-PC ratio in UC despite decreased overall PC content (lysoPC + PC) [57].…”
Section: Discussionmentioning
confidence: 65%
“…In addition, phospholipase A2 (PLA2) that catalyzes the degradation of PC to lysoPC [52], showed elevated content and activity in animal models of colitis and in actively inflamed colonic mucosa of UC patients compared to the inactively inflamed mucosa and the control [53][54][55][56]. The upregulation of PLA2 is consistent with the higher lysoPC-to-PC ratio in UC despite decreased overall PC content (lysoPC + PC) [57].…”
Section: Discussionmentioning
confidence: 65%
“…In a second trial from the same group, phosphatidylcholine was superior to placebo in steroid-refractory ulcerative colitis and the endoscopic activity was significantly improved as well [18]. Long-term follow-up of patients from 3 randomized controlled trials showed a difference after follow-up of 26 months [19]. A dose-finding study from the same group found that 1 g/day was the effective dose [20].…”
Section: Phosphatidylcholinementioning
confidence: 99%
“…Patients participating in the abovementioned trials were offered an open-label follow-up treatment after completion of each of the trials. After a mean follow-up time of 26 months, continuous remission was maintained in 33% of the PC-treated patients versus 10% of the controls (p=0.004) 33. Finally, the results of a phase IIb placebo-controlled dose-finding study with an optimised highly enriched PC preparation (LT-02; 0.8 g, 1.6 g and 3.2 g) in 156 patients with mesalazine-refractory UC were recently presented.…”
Section: Innovative Therapeutic Targets In Ucmentioning
confidence: 99%