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العنوان
plasma matrix metalloproteinaes 3&9 in Patients with ulcerative colitis as abiomarker of dsease activity /
المؤلف
Metwally, Ramy Ahmed Samy.
هيئة الاعداد
باحث / Ramy Ahmed Samy Metwally
مشرف / Alaa Eldeen Ibrahim Abd-Allah
مشرف / Fawzy Megahed Khalil
مشرف / Sherif Ismail Negm
مشرف / Gamal Mohamed Qnawy
الموضوع
Internal medicine.
تاريخ النشر
2006.
عدد الصفحات
138P. :
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
الطب الباطني
تاريخ الإجازة
1/1/2006
مكان الإجازة
جامعة بنها - كلية طب بشري - باطنه عامة
الفهرس
Only 14 pages are availabe for public view

from 142

from 142

Abstract

Ulcerative colitis is a chronic inflammatory disease of the rectum and colon . Results from many studies in people and animals of intestinal inflammation suggest that ulcerative colitis results from environmental factors triggering a loss of tolerance for normal intestinal flora in genetically susceptible individuals.

The timely breakdown of extracellular matrix (ECM) is essential for embryonic development, morphogenesis, reproduction, and tissue resorption and remodeling. The matrix metalloproteinases (MMPs) also called matrixins are thought to play a central role in these processes. The
expression of most matrixins is transcriptionally regulated by growth factors, hormones, cytokines, and cellular transformation.
The proteolytic activities of mmps are precisely controlled during activation from their precursors and inhibition by endogenous inhibitors, α-macroglobulins , and tissue inhibitors of metalloproteinases (timps).
Degradation and remodelling of the extra cellular matrix (ECM) is increasingly implicated in the pathogenesis of many inflammatory diseases such as inflammatory bowel disease, MMPs play a key role in these events.
MMPs can cleave all components of the ECM and in health act in harmony as part of normal tissue turn over. During inflammation their dysregulation leads to excess degradation of the Matrix components and loss of tissue integrity. MMPs are released from almost all connective tissue cells in response to inflammatory stimuli such as cytokines

Our study was done upon 30 patients previously diagnosed as ulcerative colitis patients 11 was in activity (6 under treatment ;steroid and mesalazine and 5 without treatment) and 19 without activity(11 under treatment and 8 without treatment) and compared with a control group of 10 subjects as plasma mean concentration of mmp3 and mmp9 was measured which denoting significant elevation of mmp3 and mmp9 in ulcerative colitis patients with active disease than those of control group and ulcerative colitis patients not in activity.
The plasma mean concentration of mmp3 & mmp9 in ulcerative colitis patients not in activity is higher than control group but statistically this difference not significant and this denoting that mmp3 and mmp9 is increasing according to disease activity so can be used as a bio marker of disease activity
In conclusion, our data confirm the role of both MMP-3 and MMP-9 in the pathogenesis of ulcerative colitis. However may be useful as a biomarker of the disease activity.