Abstract | BACKGROUND: METHODS: A randomized, controlled study was undertaken on 48 women. RESULTS:
Hysterectomy specimens were obtained and immunocytochemistry was carried out with antibodies to CD31, alpha-smooth muscle actin and myosin. Stereological measurement of blood vessels was also undertaken. Most vessels appeared normal, including the arterioles. Large thin-walled vessels were present in the superficial endometrium of the treated group but were almost completely absent in the controls. The distribution of cytoskeletal markers revealed well-formed basal arterioles with more widespread expression in the superficial stroma than was found in untreated tissue. The volume fraction of blood vessels (P = 0.0001), the number of vessel cross-sections per unit area (P = 0.0003) and the cross-sectional diameters of the largest vascular lumens (P = 0.0001) were significantly increased following treatment with LNG-IUS. However, there was no difference in the median values of vessel diameter or the vascular surface density. CONCLUSION: These findings suggest that the LNG has a localized effect on some vessels within the superficial endometrium.
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Authors | C Jay McGavigan, Peter Dockery, Vasiliki Metaxa-Mariatou, Dianne Campbell, Colin J R Stewart, Iain T Cameron, Steven Campbell |
Journal | Human reproduction (Oxford, England)
(Hum Reprod)
Vol. 18
Issue 1
Pg. 77-84
(Jan 2003)
ISSN: 0268-1161 [Print] England |
PMID | 12525444
(Publication Type: Clinical Trial, Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Chemical References |
- Actins
- Hormones
- Platelet Endothelial Cell Adhesion Molecule-1
- Levonorgestrel
- Myosins
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Topics |
- Actins
(metabolism)
- Adult
- Arterioles
(pathology)
- Blood Vessels
(pathology)
- Endometrium
(blood supply, metabolism)
- Female
- Hormones
(physiology)
- Humans
- Immunohistochemistry
- Intrauterine Devices
- Levonorgestrel
(administration & dosage, adverse effects)
- Muscle, Smooth
(metabolism)
- Myosins
(metabolism)
- Neovascularization, Physiologic
(physiology)
- Platelet Endothelial Cell Adhesion Molecule-1
(metabolism)
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