The prevalence of sPOP in this study was high, and highest in the youngest women, decreasing with age. Conversely, surgery for prolapse was negligible in this cohort of nulliparous women aged 25–64 years of age. Nulliparous women with sPOP were shorter, more often overweight and obese, and more often reported childhood nocturnal enuresis and a family history of sPOP. The cut-off point of symptom frequency to define a positive response had a decisive influence on prevalence rates, decreasing drastically with higher frequencies. In addition, the symptom of “bulging” was strongly associated with “chafing” as a symptom and also, but somewhat weaker, with co-occurring FI and urgency/OAB. The proportion of co-occurring symptoms increased linearly with increased frequency of “bulging.”
In contrast to our results, an sPOP prevalence of 0.6% was reported in subgroups of nulliparous women from two cross-sectional studies on randomly selected US women aged ≥20 years [13]. In the survey by Nygaard et al. [13], the question for sPOP was “Do you experience bulging or something falling out you can see or feel in the vaginal area?” Two out of 396 nullipara admitted this symptom. Tegerstedt et al. [15] used a postal questionnaire to assess the prevalence of POP in a survey of 5,489 randomly selected women living in the city of Stockholm. Of 1,458 nullipara (mean age 44 years), 35 (2.4%) affirmed the question, “Do you have a sensation of tissue protrusion (vaginal bulge) from the vagina?”, which is identical to the question used in the present study [15]. In a recent questionnaire study by Cooper et al. [21] from a UK community practice of women >18 years of age (parous as well as nulliparous) two questions from the International Consultation on Incontinence Questionnaire for Vaginal Symptoms (ICIQ-VS) were used to identify POP: “Are you aware of a lump or bulge coming down in your vagina?”, and “Do you feel a lump or bulge come out of your vagina, so that you can feel it on the outside or see it on the outside?”. Interestingly, the prevalence was 8.4 and 4.9% respectively [21]. These results indicate that the content, wording, and the definition of a positive response may significantly affect the prevalence rate.
In contrast to studies based on self-reporting, the prevalence of prolapse based on clinical investigations has produced more consistent results. In a few studies, mainly of convenient samples of women seeking care at outpatient clinics, the distribution of POPQ stages in nulliparous women of different ages has been described. In four studies on a total of 607 nullipara, 3 women aged <60 years had POPQ stage ≥3 (0.5%) and 20–25% had a stage 2 prolapse [9,10,11, 22]. Given a selection bias due to a health deficit that adheres to outpatient samples, these results are presumably overestimates.
Case reports on rare causes of prolapse have also been reported in nulliparous women. They form a heterogeneous group with diverse pathogenic factors, such as connective tissue disorders, previous pelvic surgery, previous pelvic fractures, spinal cord injury, prolonged severe constipation, and excessive strenuous physical activity [4,5,6,7]. We had no information in the questionnaire about these conditions.
The rarity of prolapse in nullipara is supported by register data regarding prolapse surgery. According to the Swedish GynOp Register [8], 278 (0.8%) of all reconstructive prolapse procedures during the 7-year period 2010–2016 (n = 33,124) were performed on women who claimed to be nulliparous. The study of Lo et al. reported on 1,275 surgically managed women with a prolapse of POPQ stage ≥3. In this large sample from one Taiwanese center, collected between 2005 and 2015, 8 women were nulliparous (0.55%) [5].
Although the relationship between clinical stage and the symptoms of POP is unpredictable [23], it has been shown that symptoms increase markedly once the leading edge reaches 1 cm distal to the introitus; hence, including some patients with POPQ stage 2 and all stage ≥3 [24]. Tan et al. found that women with POPQ stage 2 had symptoms in 24% at 1 cm above introitus and in 49% at the hymenal remnant [25]. Considering the predominance of stage 0 and 1 (>80%) in nulliparous women [9,10,11, 22], and a distribution that is most probably skewed toward more proximal and asymptomatic stage 0–2, the prevalence of symptoms from an anatomical prolapse should theoretically be expected to be, at most, 1–2% in nulliparous women <60 years of age.
The relationship between POPQ stage 0 and the “bulging” symptom has been studied by Tegerstedt et al. [15, 16]. In 199 women, they found that “bulging” was reported to occur “Infrequently” in 6.0%, “Sometimes” in 2.5%, and “Often” in 0%. This study is a unique natural experiment and the first to report the proportion of indisputably false-positive responses in a large group of women who did not have a clinically detectable prolapse. Further, their results are very similar to the result of the present study of 5.1, 2.4, and 0.4% (Infrequent/Sometimes/Often). This conformity is of significance as both Tegerstedt et al. and the present study used the same question for sPOP, analyzed a randomly selected Swedish population, and were conducted within a 10-year period. It therefore seems reasonable to expect that both nulliparous women <65 years of age and women without an anatomical prolapse self-report “bulging” (Infrequently/Sometimes/Often) in ≈8%. These data also show that the choice of cut-off point for symptom frequency to define a positive response is decisive for prevalence rates.
In this study, the prevalence and age-related trend of sPOP were counterintuitive, therefore suggesting a spectrum effect [26]. Unlike UI and FI, genital prolapse is not a uniform, easily definable pathological state, but rather a continuum ranging from barely existing to clearly present. Any distinction between a normal variant and the disease state of POP has been considered to be arbitrary [27], both on the basis of clinical examination [28] and as defined from diagnostic questions that are symptom-based, which are considered to be particularly prone to spectrum bias. In surveys with a low prevalence of the target condition, there may be more individuals in whom the condition is less severe and atypical [26], further increasing the likelihood of a spectrum effect. Nulliparous women, with clinical stages skewed toward “Not present” and some milder forms, may interpret the “bulging” question differently compared with those with genital prolapse beyond the hymen, having experienced the condition-specific symptom often and for a long time. For instance, in the study by Tegerstedt et al. the symptom of “bulging” was experienced “Sometimes or more often” in 85.5% of women with clinically confirmed POP and in 2.5% of women with POPQ stage 0 [16]. In our study, the prevalence of sPOP, defined by the cut-off frequency including only those having the symptom “Sometimes or more often,” was similar (2.9%).
The puzzle of false-positive responses among women without clinical prolapse has not yet been satisfactorily examined. If a prolapse is not present, the experience, which is perceived as “bulging” must be due to other conditions. The question about a bulging sensation is more likely to produce false-positive responses if there are coexisting conditions in the same anatomical location that elicit sensations mimicking and misinterpreted as the classic symptom [12, 26]. Young age (<35 years), overweight and obesity, and enuresis all had a significant, but weak association with the “bulging” symptom. The strong association between UI and prolapse in the literature [29] was not observed in this study, further indicating the absence of anatomical prolapse. The three strongest predictors for sPOP were chafing, urgency/OAB, and FI. The high prevalence of “chafing” among women in the youngest age group may be explained by their higher levels of physical and sexual activity. The association between the successive increase in prevalence and clustering of these conditions and increasing frequency of sPOP indicates that they may contribute to sensations that are perceived as “bulging” and translate into false-positive responses.
The strength of the design used for this study has been presented elsewhere [20]. The obvious limitation of this study was that the participants were not clinically evaluated for staging according to the POPQ. However, this would have been highly impractical and led to another type of selection bias [12]. The response rate increased with age from 43% among the youngest to 63% among the oldest, which is frequently observed and may simply reflect that older women are more likely to be compliant and respond. Younger women may preferentially respond because of symptoms that may introduce a bias toward the sick and inflate prevalence. The validity of self-report, upon which this study is based, depends on the participants’ willingness and ability to perceive, evaluate, and report correctly, which may also change with aging. Data on nonresponders also suggests a selection bias. Nonresponders were younger, more often immigrants or non-Swedish citizens, less often married, living in suburbs or commuting municipalities, and had a lower income and level of education. This indicates a lower socioeconomic status (SES) of the nonresponders. However, the association between SES and genital prolapse is not relevant to this study, which focuses on women with a low probability of the condition. Women in this study were predominantly Caucasians, which is why results should be interpreted with caution for diverse ethnic groups.