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Genital Chlamydia trachomatis Infection is Related to Poor Sexual ...

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1132 Cai et al.<br />

women could be then considered as a potential<br />

d<strong>is</strong>ease reservoir. Absence of symp<strong>to</strong>ms increases<br />

the r<strong>is</strong>k of infecting sexual partners and may cause<br />

long-term complications in men, <strong>to</strong>o, such as poor<br />

quality of semen and infertility [3,5]. Ct infection<br />

long-term effects include ec<strong>to</strong>pic pregnancy and<br />

tubal inflammation with subsequent infertility<br />

[4,5]. The effects of Ct infections on women’s<br />

sexual quality of life have not been previously<br />

clearly demonstrated [6], although several authors<br />

described symp<strong>to</strong>ms such as dyspareunia and<br />

vaginal d<strong>is</strong>charge as limiting fac<strong>to</strong>rs in women’s<br />

sexual life [7,8]. Other studies demonstrated that<br />

sexually transmitted d<strong>is</strong>eases (STDs) in general<br />

could have a significant impact on sexual quality of<br />

life, although these studies have been carried out<br />

on specific subject populations, such as sex workers<br />

[6] or adolescents [9,10]. The aim of the present<br />

study was <strong>to</strong> assess whether genital Ct infection<br />

could induce sexual function alterations in young<br />

sexually active women.<br />

Materials and Methods<br />

Study Design<br />

The present study was planned as cross-sectional,<br />

in line with the definition by Abramson et al. [11],<br />

<strong>to</strong> test the relationship between Ct genital infection<br />

and sexual quality of life in young women. We<br />

planned th<strong>is</strong> study as cross-sectional due <strong>to</strong> the fact<br />

that th<strong>is</strong> kind of study describes the relationship<br />

between d<strong>is</strong>eases (or other health-related states)<br />

and other fac<strong>to</strong>rs of interest as they ex<strong>is</strong>t in a specified<br />

population at a particular time, without regard<br />

<strong>to</strong> what may have preceded or precipitated the<br />

health status found at the time of the study. Female<br />

partners of patients affected by chronic bacterial<br />

prostatit<strong>is</strong> attending our STDs centre were clinically<br />

and microbiologically evaluated over the last<br />

10 years. All of them underwent microbiological<br />

analyses for common bacteria/yeasts or Ct due <strong>to</strong><br />

their sexual relationships with subjects affected by<br />

chronic bacterial prostatit<strong>is</strong>. All participants<br />

anonymously completed the Female <strong>Sexual</strong> Function<br />

Index [FSFI questionnaire], in accordance<br />

with Rosen et al. [12]. All patients were then split<br />

in<strong>to</strong> three groups, in accordance with their microbiological<br />

results: Group A—women with genital<br />

Ct infection, Group B—women with genital<br />

bacterial/yeast infection, and Group C—women<br />

negative for genital Ct infection. Data from the<br />

FSFI questionnaire were analyzed in order <strong>to</strong> test<br />

the differences among the three groups. Group A<br />

was considered as the patients group, while<br />

J Sex Med 2011;8:1131–1137<br />

Groups B and C were considered as control<br />

groups. The ratio between case and control was<br />

establ<strong>is</strong>hed as at least 1:2. The diagnos<strong>is</strong> of Ct<br />

vaginal infection was carried out in accordance<br />

with Schachter et al. [13], by using self-collected<br />

vaginal swab (VGS) and nucleic acid amplification<br />

tests. In short, we considered positive a Ct patient<br />

with VGS positive for Ct-DNA and/or anti-Ct<br />

mucosal IgA. All patients signed an informed<br />

consent form explaining the nature of the study.<br />

The women did not receive any compensation for<br />

participating in th<strong>is</strong> study. Participation was, then,<br />

voluntary and anonymous. Physical examination<br />

was not carried out in accordance with Schachter<br />

et al. [13]. Finally, in the present study, no information<br />

about therapy, clinical outcome, or<br />

follow-up data has been supplied.<br />

Inclusion and Exclusion Criteria<br />

Patient character<strong>is</strong>tics cons<strong>is</strong>ted of age between 18<br />

and 45 years, premenopausal status, absence of<br />

comorbidities, no medical treatments for pain, no<br />

genital ana<strong>to</strong>mical deformity, no previous geni<strong>to</strong>urinary<br />

surgery, no prescription drug use,<br />

regular sex life, and singular sexual partner during<br />

the last 3 months. Furthermore, all women who<br />

had undergone therapy with antibiotics, nonsteroidal<br />

anti-inflamma<strong>to</strong>ry drugs, or steroids for 4<br />

weeks prior <strong>to</strong> the study were excluded. Additional<br />

exclusion criteria were use of hormone therapy<br />

and pregnancy or lactation. Moreover, all women<br />

who were symp<strong>to</strong>matic for already known urinary<br />

or genital infections, or who had a medical h<strong>is</strong><strong>to</strong>ry<br />

of vulvar itching, f<strong>is</strong>sures, abnormal d<strong>is</strong>charge, and<br />

pers<strong>is</strong>tent pain at intercourse were also excluded.<br />

FSFI<br />

The FSFI <strong>is</strong> a brief multidimensional validated<br />

scale for assessing sexual function in women that<br />

includes 19 questions grouped in<strong>to</strong> six domains<br />

(desire, subjective arousal, lubrication, orgasm,<br />

sat<strong>is</strong>faction, and pain) with a <strong>to</strong>tal score range<br />

between 2 and 36 with higher scores indicating<br />

better functions [12]. In accordance with Giuliano<br />

et al., FSFI cu<strong>to</strong>ff score for female sexual dysfunction<br />

of 23 was used [14]. The questionnaires were<br />

self-admin<strong>is</strong>tered when the patient arrived at our<br />

centre.<br />

Sample Collection and Labora<strong>to</strong>ry Procedures<br />

All microbiological analyses were carried out in<br />

accordance with Mazzoli et al. [15]. However, in<br />

brief, from each subject, three biological samples<br />

were collected: first void early morning urine

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