Measurement of Serum and Peritoneal Levels of Amyloid Protein A and Their Importance in the Diagnosis of Pelvic Endometriosis

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2
Tipo de produção
article
Data de publicação
2013
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SCI PRINTERS & PUBL INC
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JOURNAL OF REPRODUCTIVE MEDICINE, v.58, n.9-10, p.411-416, 2013
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OBJECTIVE: To evaluate serum and peritoneal concentrations of amyloid protein A in women with endometriosis and to compare them with those of women without endometriosis. STUDY DESIGN: A prospective study evaluated 76 women suspected of having pelvic endometriosis. Fifty-seven women (group A) were confirmed by videolaparoscopy and had their serum and peritoneal amyloid A concentrations measured by procedure of evaluating the peritoneal amyloid A concentration in endometriosis merits further investigation. ELISA. The average levels from group A were compared to those obtained in group B. Group B was composed of 13 women without endometriosis, submitted to elective laparoscopy for tubal ligation. RESULTS: Peritoneal amyloid A concentrations in group A (310.3 +/- 97.8 ng/mL) were higher than those of group B (53.4 +/- 58.2 ng/mL); p = 0.0. However, serum concentrations in groups A (14.01 +/- 32.3 ng/mL) and B (9.5 +/- 15.9 ng/mL) did not differ significantly; p = 0.35. CONCLUSION: The peritoneal amyloid A protein concentration in pelvic endometriosis was higher when compared to normal controls, corroborating the inflammatory nature of the disease. This finding suggests that the procedure of evaluating the peritoneal amyloid A concentration in endometriosis merits further investigation.
Palavras-chave
amyloid A protein, diagnosis, dysmenorrhea, dyspareunia, endometriosis, infertility, pelvic pain
Referências
  1. Abbott JA, 2003, HUM REPROD, V18, P1922, DOI 10.1093/humrep/deg275
  2. Abrao MS, 2007, HUM REPROD, V22, P3092, DOI 10.1093/humrep/dem187
  3. Abrao MS, 1997, HUM REPROD, V12, P2523, DOI 10.1093/humrep/12.11.2523
  4. Agic A, 2006, GYNECOL OBSTET INVES, V62, P139, DOI 10.1159/000093121
  5. [Anonymous], 1997, FERTIL STERIL, V67, P817
  6. Bedaiwy MA, 2002, HUM REPROD, V17, P426, DOI 10.1093/humrep/17.2.426
  7. BOUTTEN A, 1992, CLIN CHIM ACTA, V210, P187, DOI 10.1016/0009-8981(92)90204-4
  8. Eskenazi B, 2001, FERTIL STERIL, V76, P929, DOI 10.1016/S0015-0282(01)02736-4
  9. FAKIH H, 1987, FERTIL STERIL, V47, P213
  10. Florio P, 2009, HUM REPROD, V24, P2600, DOI 10.1093/humrep/dep195
  11. Khan KN, 2002, ACTA OBSTET GYN SCAN, V81, P764, DOI 10.1034/j.1600-0412.2002.810814.x
  12. Malle E, 1996, EUR J CLIN INVEST, V26, P427, DOI 10.1046/j.1365-2362.1996.159291.x
  13. Mihalyi A, 2010, HUM REPROD, V25, P654, DOI 10.1093/humrep/dep425
  14. Abrao MS, 2003, INT J GYNECOL OBSTET, V82, P31, DOI 10.1016/S0020-7292(03)00079-1
  15. Skrzypczak J, 2005, EUR J OBSTET GYN R B, V122, P95, DOI 10.1016/j.ejogrb.2004.11.044
  16. Somigliana E, 2004, HUM REPROD, V19, P1871, DOI 10.1093/humrep/deh312
  17. Uhlar CM, 1999, EUR J BIOCHEM, V265, P501, DOI 10.1046/j.1432-1327.1999.00657.x
  18. Urieli-Shoval S, 2000, CURR OPIN HEMATOL, V7, P64, DOI 10.1097/00062752-200001000-00012