TY - JOUR
T1 - Cervical human papillomavirus detection is not affected by menstrual phase
AU - Tota, Joseph E.
AU - Ramanakumar, Agnihotram V.
AU - Mahmud, Salaheddin M.
AU - Trevisan, Andrea
AU - Villa, Luisa L.
AU - Franco, Eduardo L.
AU - Baggio, Maria Luiza
AU - Galan, Lenice
AU - Sobrinho, João Simão
AU - Prado, José Carlos Mann
AU - Ferreira, Silvaneide
AU - Termini, Lara
AU - Costa, Maria Cecília
AU - Miyamura, Romulo
AU - Thomann, Patricia
AU - Candeias, João
AU - Sichero, Laura
AU - Rahal, Paula
AU - Ruiz, Antonio
AU - Kaiano, Jane
AU - Santos, Monica
AU - Savio, Patricia
AU - Maciag, Paulo
AU - Rabachini, Tatiana
AU - Rousseau, Marie Claude
AU - Schlecht, Nicolas
AU - Trottier, Helen
AU - Ferenczy, Alex
AU - Rohan, Thomas
AU - Chevarie-Davis, Myriam
AU - Duarte, Eliane
AU - Kulaga, Sophie
AU - Robitaille, Juliette
AU - Platt, Robert
PY - 2013/5
Y1 - 2013/5
N2 - Objectives: In many settings, human papillomavirus (HPV) DNA testing already plays an important role in cervical cancer screening. It is unclear whether hormonal fl uctuations associated with menstrual phase or oral contraceptive (OC) use have any effect on HPV detection. We evaluated the effects of OC use and timing of cervical sampling in relation to women' s last menstrual period (LMP) on HPV detection, and viral load in the Brazilian Ludwig - McGill cohort study. Methods: Women in the cohort were followed every 4-6 months, and at each clinic visit they were asked to complete a questionnaire and to provide a cervical sample for HPV testing. Specimens from 6093 patient visits (n=2209 women) were categorised according to date of LMP into four distinct phases: follicular (days 5-9), midcycle (days 10-15), luteal (days 16-22), or late luteal (days 23-31). Results: Compared with follicular phase (referent group), HPV detection did not differ according to reported LMP for midcycle (OR=1.14, 95% CI 0.95 to 1.37), luteal (OR=1.03, 95% CI 0.85 to 1.25), or late luteal menstrual phase (OR=1.01, 95% CI 0.83 to 1.24), and was also not influenced by OC use. Analyses restricted to high-risk HPV types (grouped) and HPVs 16 and 18 (separately), produced similar non-signi fi cant associations. For HPV-positive samples, we found that the menstrual phase did not influence the total viral load. Conclusions: These results indicate HPV detection is not associated with menstrual phase. Our findings suggest that standardising the timing of specimen collection for HPV testing is not necessary.
AB - Objectives: In many settings, human papillomavirus (HPV) DNA testing already plays an important role in cervical cancer screening. It is unclear whether hormonal fl uctuations associated with menstrual phase or oral contraceptive (OC) use have any effect on HPV detection. We evaluated the effects of OC use and timing of cervical sampling in relation to women' s last menstrual period (LMP) on HPV detection, and viral load in the Brazilian Ludwig - McGill cohort study. Methods: Women in the cohort were followed every 4-6 months, and at each clinic visit they were asked to complete a questionnaire and to provide a cervical sample for HPV testing. Specimens from 6093 patient visits (n=2209 women) were categorised according to date of LMP into four distinct phases: follicular (days 5-9), midcycle (days 10-15), luteal (days 16-22), or late luteal (days 23-31). Results: Compared with follicular phase (referent group), HPV detection did not differ according to reported LMP for midcycle (OR=1.14, 95% CI 0.95 to 1.37), luteal (OR=1.03, 95% CI 0.85 to 1.25), or late luteal menstrual phase (OR=1.01, 95% CI 0.83 to 1.24), and was also not influenced by OC use. Analyses restricted to high-risk HPV types (grouped) and HPVs 16 and 18 (separately), produced similar non-signi fi cant associations. For HPV-positive samples, we found that the menstrual phase did not influence the total viral load. Conclusions: These results indicate HPV detection is not associated with menstrual phase. Our findings suggest that standardising the timing of specimen collection for HPV testing is not necessary.
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U2 - 10.1136/sextrans-2012-050610
DO - 10.1136/sextrans-2012-050610
M3 - Article
C2 - 23112338
AN - SCOPUS:84878166539
SN - 1368-4973
VL - 89
SP - 202
EP - 206
JO - Sexually Transmitted Infections
JF - Sexually Transmitted Infections
IS - 3
ER -