Literature DB >> 35804377

Incidence and risk factors of infertility among couples who desire a first and second child in Shanghai, China: a facility-based prospective cohort study.

Chenfeng Zhu1,2,3,4, Li Yan1,3,4, Chuqing He1,3,4, Yang Wang1,3,4, Jiahao Wu2, Luting Chen5,6,7, Jian Zhang8,9,10.   

Abstract

BACKGROUND: With the implementation of the two-child policy in China, more couples have expressed the desire to have another child. We conducted this study to evaluate the incidence of infertility and risk factors in couples intending to have a first and second child.
METHODS: From 2013 to 2017, a prospective cohort study was conducted at the pre-pregnancy center of the International Peace Maternal and Child Health Hospital. The participants were selected by screening and random sampling couples who came to the pre-pregnancy center. Data regarding patient sociodemographic characteristics, reproductive and gynecological history, male disease history, and laboratory and imaging examination results were collected. Couples were followed up every 3 months until pregnancy or for 12 months, whichever came first. Multi-factor logistic regression was used to analyze risk factors for infertility. Adjusted odds ratios (aORs) and corresponding 95% confidence intervals (CIs) were calculated and adjusted for potential confounding factors.
RESULTS: The overall infertility incidence was 16.95% (369/2177). The infertility incidence of "first child intention" and "second child intention" was 19.30% (355/1839) and 4.14% (14/338), respectively. This study found great differences in both infertility rate (P < 0.001) and risk factors between the two groups. Risk factors for "first child intention" infertility included advanced age (> 35 years) (aOR = 1.70, 95% CI 1.27-2.28), abnormal body mass index (BMI) (aOR = 1.58, 95% CI 1.31-6.26), longer menstrual periods (aOR = 4.47, 95% CI 2.25-8.88), endometrial polyps (aOR = 2.52, 95% CI 1.28-4.97), polycystic ovarian syndrome (PCOS) (aOR = 6.72, 95% CI 1.79-7.39), salpingostomy (aOR = 3.44, 95% CI 1.68-7.07), and history of mycoplasma (aOR = 1.54, 95% CI 1.09-2.40). However, in the "second child intention" group, clinical risk factors slightly differed and included leiomyoma (aOR = 5.60, 95% CI 1.06-29.76), and higher age (> 40 years) (aOR = 7.36, 95% CI 1.01-53.84).
CONCLUSION: The overall infertility rate in Shanghai is similar to that of other large cities in China. Marriage at advanced ages has become increasingly common. As such, the government must consider subsidies to encourage childbirth at childbearing ages, which can improve fertility levels.
© 2022. The Author(s).

Entities:  

Keywords:  Epidemiology; First child intention; Incidence; Infertility; Risk factor; Second child intention

Mesh:

Year:  2022        PMID: 35804377      PMCID: PMC9270756          DOI: 10.1186/s12978-022-01459-x

Source DB:  PubMed          Journal:  Reprod Health        ISSN: 1742-4755            Impact factor:   3.355


Background

Infertility is a common medical problem, though its influencing factors have not been elucidated [1]. However, previous studies have found that diseases of the reproductive system and social and psychological factors contribute to infertility [2, 3]. Additionally, due to differences in region, environment, and economy, infertility incidence significantly varies around the world [4, 5]. Previous studies have found that 12-month infertility rates were 15.6% (2009–2010) and 10.5% (2007) in Canada and Scotland, respectively [6, 7]. The overall prevalence of infertility in Iran was 8% in 2006 [8]. A 2007 survey in China involving 17,275 women from 8 provinces estimated that the overall infertility rate was 15.6% [9], while the infertility rate in Shanghai was 9% in 2002 [10]. However, these results were based on data that are now outdated, and the current infertility rate in Shanghai is unknown. Infertility is a national concern that causes emotional, financial, and societal burdens [11]. Surveys have shown that the financial burden of infertility in China in 2008 was approximately 11.4 billion to 32.5 billion dollars [12]. Infertility rates have continued to increase in the Chinese population, from 6.7% in 2005 to 15.5% in 2018 [9]. As the incidence of infertility increases, so does its societal burden. By the end of 2018, 497 assisted reproductive technology (ART) centers were approved by the Chinese government; the total number of human ART cycles per year has exceeded 1 million, and the number of babies born has exceeded 300,000 [13]. Therefore, infertility is a problem that requires urgent attention. According to the World Health Organization (WHO) definition, infertility is the failure to become pregnant after at least 12 months of regular unprotected sexual intercourse [14]. Primary infertility is defined as infertile couples with no pregnancy history, while secondary infertility is defined as infertile couples with a history of pregnancy [15]. Compared with primigravida, increasing age and other potential factors can compromise the fertility of women who intend to have a second child. Recent research has focused on the prevalence and risk factors for primary and secondary infertility [16], though too little attention has been paid to the infertility of couples intending to have a second child. Since China implemented the second-child policy, approximately 90 million women have been allowed to have a second child [17]. Moreover, recent evidence has demonstrated that of these 90 million women, approximately 60% are over 35, and 50% are over 40 [18]. Therefore, we performed a prospective cohort study in Shanghai, based on a few researchers investigating infertility incidence in the past 15 years to evaluate the incidence and risk factors of infertility in couples intending to have a first or second child.

Materials and methods

Study design and participants

We performed a single-center, prospective cohort study in pre-pregnancy centers in Shanghai, China, from January 2013 to December 2017. Since 2012, China has performed pre-pregnancy check-ups, prompting couples trying to become pregnant to seek services from these institutions [19]. These pre-pregnancy centers provide pre-pregnancy education, consultation, and ordinary examinations (including infectious diseases and reproductive system examination for women) for couples of childbearing age in surrounding communities. The inclusion criteria included: (1) aged 20 to 49 years; (2) couples who intend to become pregnant and engage in regular sexual activity over the following year. The exclusion criteria included: (1) BMI < 17 or > 33 kg/m2); (2) couples who did not plan to become pregnant or had a history of infertility; (3) couples whose laboratory findings did not allow them to be pregnant within the next year or those who planned to have a third child or more. Written informed consent was obtained from all participants.

Procedures

Based on the inclusion and exclusion criteria, proportionate sampling was used to select the study participants, who were recruited couples of childbearing ages who came to the pre-pregnancy center from January 2013 to December 2017. Participants were recruited by random sampling in an equal ratio (15:1) from the eligible population based on the order they came to the hospital. After informed consent was obtained, information was collected from each participant by a trained investigator, including sociodemographic characteristics (e.g., age, marital status, education, occupation, individual annual income, smoking status), history of reproduction, and gynecology (e.g., number of pregnancies, pregnancy outcomes, age at menarche, menstrual cycle, menstrual duration, menstrual blood volume, medical history, operative history), disease history of the male (e.g., medical history, operative history), and pre-pregnancy medical examination results (e.g., serological antibody, pelvic ultrasound). Follow-ups to assess pregnancy outcomes were evaluated by telephone or face-to-face interviews. Follow-ups were performed by a well-trained investigator via telephone every 3 months until delivery or for 12 months, whichever came first. Follow-up questionnaires included: Are you currently pregnant? When was the last menstrual period before pregnancy? How long have you been pregnant, and have you identified any new gynecological disorders? Our study defined infertility as not becoming pregnant through regular sex without contraception for at least 12 months. Based on whether participants were infertile, couples intending to have a first child were then classified into the “infertility of first child intention” group and the “fertility of first child intention” group. During the same study period, couples intending to have a second child were classified into the “infertility of second child intention” group and the “fertility of second child intention” group. According to the definition of infertility, the infertility incidence was calculated as the number of infertile women divided by the number of women intending to become pregnant.

Statistical analysis

Based on a previous pilot study and relevant studies [9, 10], we assumed that the infertility rate among couples was 15%. With an error margin of 2% and a two-sided 95% confidence interval (CI), this required total sample size of 1273. To minimize the sampling error, we calculated a final sample size that was 1.5-fold the previous one, resulting in a total sample size of 2000. Infertility was considered a binary outcome, and corresponding 95% CIs were calculated assuming a binomial distribution of the observed number of events. Univariable conditional logistic regression analysis was also used to calculate crude odds ratios (ORs) and 95% CIs. Multivariable logistic regression analysis was performed to explore potential risk factors and corresponding ORs. Before constructing the logistic regression model, a multicollinearity analysis was performed between independent variables included in the regression models. We chose the covariates examined by multivariable logistic regression based on their clinical relevance to infertility and the results of univariate analysis. Forward stepwise regression was used to combine factors related to infertility (female age and BMI, male BMI, menstrual duration, female medical history of leiomyoma, endometrial polyp, PCOS, endometriosis, salpingostomy, and chlamydia genitalium) in a multivariate regression model [20]. Statistical analysis was performed using IBM SPSS Version 21.0 (IBM Corp., Armonk, NY, USA). All p-values were estimated using two-sided tests, and differences were considered statistically significant when p < 0.05.

Results

From January 2013 to December 2017, 35,000 couples visited the pre-pregnancy center. After excluding 846 couples who were pregnant and 120 couples with extreme BMI values, 2300 participants in the cohort were selected from 34,034 couples at a 15:1 ratio. However, 48 (2.09%) couples who were worried about disclosing their private information refused to participate in the investigation, 64 (2.78%) were lost during the follow-up period, and 11 (0.50%) couples already had two or more children. Finally, 1839 couples intending to have a first child and 338 couples intending to have a second child were included in this study (recruitment flow chart is shown in Fig. 1).
Fig. 1

Recruitment profile of the study

Recruitment profile of the study

Baseline characteristics

Table 1 shows the differences in the sociodemographic and socioeconomic characteristics of couples in this study. The mean (± standard deviation [SD]) age was 29.76 (± 3.71) years for all women and 31.36 (± 4.39) years for all men. Among couples with “first child intention,” the mean (± SD) age was 29.50 (± 3.52) for women and 31.12 (± 4.22) for men. Among couples with “second child intention,” the female and male mean (± SD) ages were 31.11 (± 4.36) and 32.53 (± 4.97), respectively. Furthermore, the mean BMI (± SD) values for all women and men were 21.08 (± 2.69) kg/m2 and 23.67 (± 2.82) kg/m2, respectively. Among couples with “first child intention,” the mean BMI (± SD) was 21.07 (± 2.70) kg/m2 for women and 23.71 (± 2.87) kg/m2 for men. Among couples with “second child intention,” the mean BMI (± SD) was 21.15 (± 2.60) kg/m2 for women and 23.52 (± 2.59) kg/m2 for men.
Table 1

Sociodemographic characteristics of study participants

All couplesP value dFertility (N = 324)Infertilitya (N = 14)P valued
N = 2177Fertility (N = 1484)Infertilitya (N = 355)
nb%nb (%)nb(%)nb(%)nb(%)
Age, years, women
 20–241336.1192 (6.23)19 (5.35)< 0.00121 (6.50)1 (7.14)0.038
 25–29109650.34818 (55.38)153 (43.10)112 (34.67)4 (28.57)
 30–3474334.13475 (32.16)137 (38.59)124 (38.39)4 (28.57)
 35–391768.0884 (5.69)38 (10.70)58 (17.96)3 (21.43)
 ≥ 40291.338 (0.54)8 (2.25)8 (2.48)2 (14.29)
Age, years, men
 20–24552.7938 (2.96)6 (1.99)0.0029 (3.02)1 (8.33)0.631
 25–2971536.31526 (41.03)97 (32.12)88 (29.53)2 (16.67)
 30–3478239.72533 (41.58)126 (41.72)111 (37.25)5 (41.67)
 35–3932816.66142 (11.15)55 (18.21)62 (20.81)2 (16.67)
 ≥ 40894.5242 (3.28)18 (5.96)27 (0.34)2 (16.67)
BMIc kg/m2, women
 < 18.5372.03180 (14.42)35 (11.36)< 0.00140 (13.70)2 (15.38)0.905
 18.5–23.9102256.18939 (75.24)202 (65.58)213 (72.95)10 (76.92)
 24–26.954529.96105 (8.41)47 (15.26)29 (9.93)1 (7.69)
 ≥ 2721511.8224 (1.92)24 (7.79)10 (3.42)0
BMIc kg/m2, men
 < 18.5372.0324 (2.00)11 (3.65)0.0082 (0.69)00.792
 18.5–23.9102256.18691 (57.44)142 (47.18)175 (60.14)8 (66.67)
 24–26.954529.96342 (28.43)101 (33.55)93 (31.96)4 (33.33)
 ≥ 2721511.82146 (12.14)47 (15.61)21 (7.22)0
Occupation, women
 Employed176890.951210 (92.30)284 (91.91)0.950256 (85.62)11 (84.62)0.343
 Self-employed844.3246 (3.51)12 (3.88)21 (7.02)2 (15.38)
 Unemployed924.7355 (4.20)13 (4.21)22 (7.36)0
Education attainment, women
 High school or low1196.0865 (4.95)26 (8.33)0.03924 (7.82)4 (30.77)0.016
 Junior college or university153478.391029 (78.37)243 (77.88)244 (79.48)8 (61.54)
 Graduate or above30415.53219 (16.68)43 (13.78)39 (12.70)1 (7.69)
Education attainment, men
 High school or low1105.6958 (4.46)20 (6.60)0.10628 (9.157)4 (30.77)0.030
 Junior college or university147176.101002 (77.14)239 (78.88)214 (69.93)8 (61.54)
 Graduate or above35218.21239 (18.40)44 (14.52)64 (20.92)1 (7.69)
Average monthly incomes (¥) of each couple
 < 10,0001176.3561 (4.94)27 (9.41)0.01227 (9.15)1 (7.69)0.903
 10,000–20,00042423.02299 (24.21)62 (21.60)58 (19.66)2 (15.38)
 > 20,000130170.63875 (70.85)198 (68.99)210 (71.19)10 (76.92)

aFaliure to conceive after regular unprotected sexual intercourse for 1 year

bThe sum does not necessarily equal the sample size for all variables because of missing data

cBMI is defined as Body mass index; Body mass index is defined as weight in kilograms divided by the square of height in meters

dPearson’s χ2 test

Sociodemographic characteristics of study participants aFaliure to conceive after regular unprotected sexual intercourse for 1 year bThe sum does not necessarily equal the sample size for all variables because of missing data cBMI is defined as Body mass index; Body mass index is defined as weight in kilograms divided by the square of height in meters dPearson’s χ2 test Most couples completed had a junior college, university, or high level of education. More than 90% of the women were employed, and most households had annual incomes exceeding 20,000 yuan. In the “couples with first child intention” group, there were more couples that were older, had a higher BMI, and had lower incomes in the infertility group than in the fertility group. Furthermore, women in this group with lower education were more likely to be infertile. In the “couples with second child intention” group, the infertility group had older, lower-educated women and lower-educated men.

The incidence of infertility

Among all couples who planned to become pregnant (n = 2177, the overall incidence of infertility was 16.95% (95% CI 15.37–18.53%; infertility = 369, fertility = 1803). The incidence of “infertility of first child intention” was 19.30% (95% CI 17.50–21.11%; infertility = 355, fertility = 1484). In contrast, the incidence of “infertility of second child intention” was 4.14% (95% CI 2.01–6.28%; infertility = 14, fertility = 324). The infertility rate between the two groups was statistically different (P < 0.001). Figure 2 shows Kaplan–Meier curves of time to pregnancy between the “first child intention” group and “second child intention” group. The “second child intention” group became pregnant faster and had a lower infertility rate than the “first child intention” group (log-rank P < 0.001).
Fig. 2

Kaplan–Meier curve for time to pregnancy. Kaplan–Meier curve for time to pregnancy according to child intention. Quicker to get pregnant is indicated for women with second child intention (log-rank P < 0.001)

Kaplan–Meier curve for time to pregnancy. Kaplan–Meier curve for time to pregnancy according to child intention. Quicker to get pregnant is indicated for women with second child intention (log-rank P < 0.001) We also calculated annual infertility rates based on the year participants were enrolled and found that the infertility rate increased each year (Fig. 3, 2013: 15.2%; 2014: 16.8%; 2015: 19.1%; 2016: 21.4%; 2017: 21.3%). (Trend P test < 0.01).
Fig. 3

Infertility rates in different years (2013: 15.2%; 2014: 16.8%; 2015: 19.1%; 2016: 21.4%; 2017: 21.3%) (Trend P test < 0.01)

Infertility rates in different years (2013: 15.2%; 2014: 16.8%; 2015: 19.1%; 2016: 21.4%; 2017: 21.3%) (Trend P test < 0.01)

Univariate analysis

Table 2 shows the crude unadjusted ORs and their 95% CIs for the relationship between infertility and female medical history. In the “couples with first child intention” group, women with a longer menstrual cycle and longer menstrual periods were more likely to be infertile compared with women who had normal menstrual periods. Regarding the medical history, infertility was associated with factors such as leiomyoma, ovarian cysts, endometrial polyps, endometriosis, polycystic ovarian syndrome (PCOS), and a history of lower genital tract infections (mycoplasma, chlamydia, and condyloma acuminate). Moreover, among infertile couples, many women had a history of surgery such as uterine myomectomy, salpingostomy, transcervical polyp resection, and hysteroscopic adhesiolysis, which were associated with a significantly higher risk of infertility. In the “couples with second child intention” group, the crude OR of infertility in women with later menarche and history of leiomyoma was significantly lower than that of women who did not.
Table 2

Menstrual and medical history of women

All couplesP valuecFirst child intentionP valuecSecond child intentionP valuec
Infertilitya (N = 369)Fertility (N = 1808)Infertilitya (N = 355)Fertility (N = 1484)Infertilitya (N = 14)Fertility (N = 324)
nb (%)nb (%)nb (%)nb (%)nb (%)nb (%)
Menstrual history
 Menarche (year)
  < 1349 (14.63)225 (13.71)0.10146 (14.56)171 (12.85)0.3192 (14.29)53 (17.32)< 0.001
  13–14245 (73.13)1273 (77.57)234 (74.05)1037 (12.85)7 (50.00)234 (76.47)
  > 1441 (12.23)143 (8.71)36 (11.39)123 (9.24)5 (35.71)19 (6.21)
 Menstrual cycle (days)
  21–35278 (81.52)1556 (93.29)< 0.001259 (80.43)289 (92.99)< 0.00114 (100.00)289 (94.44)1.000
  > 3563 (18.48)112 (6.72)63 (19.57)95 (7.01)0 (0)17 (5.56)
 Menstrual duration (days)
  2–7317 (92.69)1629 (97.60)< 0.001299 (92.57)1328 (98.23)< 0.00113 (92.86)294 (95.77)0.471
  > 725 (7.31)40 (2.40)24 (7.43)24 (1.77)1 (7.14)13 (4.23)
 Dysmenorrhea
  None148 (43.529)728 (43.776)0.936139 (43.30)568 (42.14)0.8948 (57.14)157 (50.97)0.903
  Occasional107 (31.471)508 (30.547)102 (31.78)428 (31.75)3 (21.43)76 (24.68)
  Regular85 (25.000)427 (25.676)80 (24.92)352 (26.11)3 (21.43)75 (24.35)
Gynecological history
 Pelvic inflammationd
  No320 (93.84)1590 (95.21)0.292303 (93.81)1292 (95.56)0.19112 (92.31)293 (94.21)0.551
  Yes21 (6.16)80 (4.79)20 (6.19)60 (4.44)1 (7.69)18 (5.79)
 Adenomyosisd
  No340 (97.98)1671 (99.10)0.047335 (97.95)1426 (99.03)0.15714 (100)318 (100)NA
  Yes7 (2.02)14 (0.83)7 (2.05)14 (0.97)0 (0)0 (0)
 Leiomyomad
  No301 (83.15)1607 (90.84)< 0.001287 (83.67)1301 (90.16)0.00110 (71.43)299 (93.73)0.013
  Yes61 (16.85)162 (9.16)56 (16.33)142 (9.84)4 (28.57)20 (6.27)
 Ovarian cystd
  No308 (85.32)1624 (91.96)< 0.001293 (85.67)1328 (92.16)< 0.00113 (92.86)291 (91.51)1.000
  Yes53 (14.68)142 (8.04)49 (14.33)113 (7.84)1 (7.14)27 (8.49)
 Endometrial polypd
  No309 (90.62)1616 (97.12)< 0.001291 (90.37)1307 (97.10)< 0.00113 (92.86)304 (97.75)0.3
  Yes32 (9.38)48 (2.89)31 (9.63)39 (2.90)1 (7.14)7 (2.25)
 Endometriosisd
  No320 (93.57)1637 (98.08)< 0.001304 (94.12)1320 (97.71)0.00213 (92.86)310 (99.68)0.084
  Yes22 (6.43)32 (1.92)19 (5.88)31 (2.29)1 (7.14)1 (0.32)
 PCOSd
  No311 (86.15)1721 (97.51)< 0.001292 (85.38)1407 (97.71)< 0.00114 (100)307 (96.54)1.000
  Yes50 (13.85)44 (2.49)50 (14.62)33 (2.29)0 (0)11 (3.46)
Surgical history
 Uterine myomectomye
  No335 (96.54)1670 (99.05)0.001317 (96.65)1352 (98.98)0.00414 (100)311 (99.36)1.000
  Yes12 (3.46)16 (0.95)11 (3.35)14 (1.02)0 (0)2 (0.64)
 Salpingostomye
  No323 (93.08)1663 (98.64)< 0.00113 (92.86)1347 (98.61)< 0.00113 (92.86)309(98.72)0.198
  Yes24 (6.92)23 (1.36)22 (6.71)19 (1.39)1 (7.14)4(1.28)
 Endometrial polypectomye
  No333 (95.97)1666 (98.81)< 0.001315 (96.04)1349 (98.76)0.00414 (100)309 (98.72)1.000
  Yes14 (4.04)20 (1.19)13 (3.96)17 (1.24)0 (0)4 (1.28)
 Hysteroscopic adhesiolysise
  No339 (97.70)1673 (99.23)0.037320 (97.56)1354 (99.12)0.03914 (100)312 (99.68)NA
  Yes8 (2.31)13 (0.77)8 (2.44)12 (0.88)0 (0)1 (0.32)
Genital tract infection history
 TPe
  No345 (99.424)1682 (99.763)0.605341 (99.42)1446 (99.72)0.32314 (100)320 (100)NA
  Yes2 (0.576)4 (0.237)2 (0.58)4 (0.28)0 (0)0 (0)
 Herpes viruse
  No345 (99.424)1685 (99.941)0.077341 (99.42)1449 (99.93)0.09614 (100)320 (100)NA
  Yes2 (0.576)1 (0.059)2 (0.58)1 (0.07)0 (0)0 (0)
 Mycoplasma genitaliume
  No291 (80.387)1504 (84.637)0.045274 (79.88)1220 (84.14)0.06413 (92.86)278 (86.88)1.000
  Yes71 (19.613)273 (15.363)69 (20.12)230 (15.86)1 (7.14)42 (13.13)
 Chlamydia genitaliume
  No340 (93.923)1716 (96.894)0.006321 (93.59)1396 (96.61)0.01014 (100)313 (98.12)1.000
  Yes22 (6.077)55 (3.106)22 (6.41)49 (3.39)0 (0)6 (1.88)
 Condyloma acuminatae
  No343 (98.847)1681 (99.703)0.081339 (98.83)1446 (99.72)0.04814 (100)319 (99.69)NA
  Yes4 (1.153)5 (0.297)4 (1.17)4 (0.28)0 (0)1 (0.31)
 HPVe
  No341 (98.271)1663 (98.636)0.784338 (98.54)1433 (98.83)0.59314 (100)314 (98.13)1.000
  Yes6 (1.729)23 (1.364)5 (1.46)17 (1.17)0 (0)6 (1.88)

PCOS polycystic ovarian syndrome, TP treponema pallidum antibody, HPV high-risk human papillomavirus

aFaliure to conceive after regular unprotected sexual intercourse for 1 year

bThe sum does not necessarily equal the sample size for all variables because of missing data

cPearson’s χ2 test

dThe diagnosis standard referred to the Dutch Rotterdam diagnostic criteria

eMake negative results as reference groups

Menstrual and medical history of women PCOS polycystic ovarian syndrome, TP treponema pallidum antibody, HPV high-risk human papillomavirus aFaliure to conceive after regular unprotected sexual intercourse for 1 year bThe sum does not necessarily equal the sample size for all variables because of missing data cPearson’s χ2 test dThe diagnosis standard referred to the Dutch Rotterdam diagnostic criteria eMake negative results as reference groups Regarding male disease history (Table 3), prostatitis and lower genital tract infection (mycoplasma and chlamydia) were factors that were associated with infertility in the “first child intention” group. However, no significant differences were found in male disease history in the “second child intention” group between infertility and fertility.
Table 3

Medical history of men all included

All couplesFirst childP valuecSecond childP valuec
Fertility (N = 1808)Infertilitya (N = 369)Fertility (N = 1484)Infertilitya (N = 355)Fertility (N = 324)Infertilitya (N = 14)
nb (%)nb(%)nb (%)nb(%)nb (%)nb(%)
Genital tract infection history
 Neisseria gonorrhoeae
  No1682 (99.94)346 (100.00)1362 (99.93)327 (100.00)1.000313 (100.00)14 (100.00)NA
  Yes1 (0.06)01 (0.07)0 (0.00)0 (0.00)0 (0.00)
 TP
  No1683 (100.00)346 (100.00)1363 (100.00)327 (100.00)NA313 (100.00)14 (100.00)NA
  Yes000 (0.00)0 (0.00)0 (0.00)0 (0.00)
 Herpes virus
  No1681 (99.88)346 (100.00)1362 (99.93)327 (100.00)1.000312 (99.68)14 (100.00)1.000
  Yes2 (0.12)01 (0.07)0 (0.00)1 (0.32)0 (0.00)
 Mycoplasma genitalium
  No1648 (97.92)328 (94.80)1331 (97.65)310 (94.80)0.009310 (99.04)13 (92.86)0.161
  Yes35 (2.08)18 (5.20)32 (2.35)17 (5.20)3 (0.96)1 (7.14)
 Chlamydia genitalium
  No1658 (98.51)267 (96.04)1340 (98.31)314 (96.02)0.017311 (99.36)14 (100.00)1.000
  Yes25 (1.49)13 (3.76)23 (1.69)13 (3.98)2 (0.64)0 (0.00)
 HPV
  No1682 (99.94)345 (99.71)1362 (99.93)326 (99.69)0.350313 (100.00)14 (100.00)NA
  Yes1 (0.06)1 (0.29)1 (0.07)1 (0.31)0 (0.00)0 (0.00)
 Prostatitis
  No1627 (97.66)321 (94.69)1312 (97.35)304 (95.00)0.050308 (99.35)13 (92.86)0.124
  Yes39 (2.34)18 (5.31)37 (2.74)16 (5.00)2 (0.65)1 (7.14)

TP treponema pallidum antibody, HPV high-risk human papillomavirus

aFaliure to conceive after regular unprotected sexual intercourse for 1 year

bThe sum does not necessarily equal the sample size for all variables because of missing data

cPearson’s χ2 test

Medical history of men all included TP treponema pallidum antibody, HPV high-risk human papillomavirus aFaliure to conceive after regular unprotected sexual intercourse for 1 year bThe sum does not necessarily equal the sample size for all variables because of missing data cPearson’s χ2 test

Multivariate analysis of risk factors for infertility

Multicollinearity diagnosis was performed before multivariate analysis, and there was no significant collinearity among the factors included in the multivariate analysis (Additional file 1: Table S1). Table 4 displays the multivariate analysis of infertility risk. For couples intending to have their first child, high BMI (≥ 24 kg/m2) and older age (> 35 years) for women and low BMI (< 18.5 kg/m2) for men were risk factors for infertility. As for female menstrual history, our results indicated that women with longer menstrual durations (OR = 4.47, 95% CI 2.25–8.88) were at a greater risk for infertility. Moreover, women with a history of endometrial polyps (OR = 2.52, 95% CI 1.28–4.97), PCOS (OR = 6.72, 95% CI 1.79–7.39), endometriosis (OR = 2.52, 95% CI 1.27–4.97), or mycoplasma infection in the lower genital tract (OR = 1.54, 95% CI 1.09–2.40) were more likely to experience infertility than women who did not. Additionally, previous salpingostomy (OR = 3.44, 95% CI 1.68–7.07) was also associated with a higher risk of infertility.
Table 4

Multivariable logistic regression analysis predicting risk factors for infertility

All couplesFirst childSecond child
AOR [95% CI]P valueAOR [95% CI]P valueAOR [95% CI]P value
Age, years, women
 20–24Reference0.008Reference< 0.001Reference0.040
 25–291.41 [0.64, 3.09]1.23 [0.67, 2.12]1.02 [0.57, 1.86]
 30–341.96 [0.89, 4.32]1.54 [0.87, 3.01]0.97 [0.45, 1.34]
 35–392.09 [0.88, 4.96]1.70 [1.27, 2.28]0.55 [0.13, 2.46]
 ≥ 405.93 [1.79, 19.67]7.89 [2.41, 25.79]7.36 [1.01, 53.84]
BMI, kg/m2, women
 < 18.51.20 [0.78, 1.84]0.0171.06 [0.68, 1.64]0.0171.46 [0.14, 15.70]0.894
 18.5–23.9ReferenceReferenceReference
 24–27.91.39 [0.90, 2.13]1.58 [1.01, 2.45]0.52 [0.05, 5.82]
 ≥ 282.73 [1.40, 5.32]2.86 [1.31, 6.26]NA
BMI, kg/m2, men
 < 18.53.41 [1.51, 7.71]0.0333.09 [1.42, 6.74]0.017NA0.965
 18.5–23.9ReferenceReferenceReference
 24–27.91.11 [0.81, 1.52]1.37 [0.99, 1.90]1.47 [0.35, 6.23]
 ≥ 281.07 [0.70, 1.65]1.26 [0.82, 1.94]NA
Menstrual duration, days
 < 2NA0.035NA< 0.001NA
 2–7ReferenceReferenceReference0.998
 > 72.34 [1.23, 4.45]4.47 [2.25, 8.88]0.99 [0.10, 9.89]
Leiomyoma
 NoReference0.013Reference0.119Reference0.043
 Yes1.66 [1.11, 2.46]1.38 [0.92, 2.07]5.60 [1.06, 29.76]
Endometrial polyp
 NoReference< 0.001Reference< 0.001Reference0.578
 Yes2.87 [1.67, 4.94]2.52 [1.28, 4.97]1.99 [0.18, 22.32]
PCOS
 NoReference< 0.001Reference< 0.001NA
 Yes3.89 [2.28, 6.64]6.72 [1.79,7.39]NA
Endometriosis
 NoReference< 0.001Reference0.001NA
 Yes3.65 [1.92, 6.95]2.52 [1.27, 4.97]NA
Salpingostomy
 NoReference< 0.001Reference< 0.001Reference0.130
 Yes4.04 [2.04, 7.98]3.44 [1.68, 7.07]9.28 [0.52, 166.22]
Chlamydia genitalium, women
 NoReference0.024Reference0.015Reference0.587
 Yes1.96 [1.09, 3.52]1.54 [1.09, 2.40]0.53 [0.05, 5.20]

BMI body mass index, PCOS polycystic ovarian syndrome, AOR adjusted odds ratio, CI confidence interval

Nagelkerke R2 = 0.622

Multivariable logistic regression analysis predicting risk factors for infertility BMI body mass index, PCOS polycystic ovarian syndrome, AOR adjusted odds ratio, CI confidence interval Nagelkerke R2 = 0.622 Regarding the “second-child intention” group, the ORs were statistically significant when females aged over 40 (OR = 7.36, 95% CI 1.01–53.84), while the female history of leiomyoma (OR = 5.60, 95% CI 1.06–29.76) was a significant risk factor for infertility in the “couples with second child intention” group, and was not significantly different in the “couples with first child intention” group (OR = 1.38, 95% CI = 0.92–2.07).

Discussion

The overall incidence of infertility was 16.95% in Shanghai, which is much higher than the infertility rate reported in Shanghai 15 years ago. Our study found the incidence of “first child intention” and “second child intention” infertility as 19.30% and 4.14%, respectively. To our knowledge, this is the first study analyzing infertility incidence and risk factors in couples intending to have a first and second child. As seen from the above infertility rate, the infertility incidence of “second child intention” is significantly lower than that of “first child intention.” Our study also found differences in infertility risk factors between the two groups. For couples with “first child intention,” obesity (BMI ≥ 24 kg/m2), advanced age (> 30 years old), female gynecological diseases such as endometrial polyps, PCOS, endometriosis, mycoplasma infection of the lower reproductive tract, and previous surgical history of tubal infertility were all associated with infertility. For couples with “second child intention,” only the following variables were significantly related to infertility: age over 40 and leiomyoma. Age is one of the causes of infertility [21]. In our study, women intending to have a first child, aged 35–39, were associated with a higher risk of infertility. In the “second child intention” group, couples 40 years and older were significantly associated with infertility. There could be three major reasons for this: (1) women with “second child intention” experienced a successful pregnancy, which suggests that these couples have a complete chain from the production of eggs and sperm to the success of pregnancy; (2) older women are less likely to develop new ovulatory dysfunction [22]. Based on the rapid decline in fertility of women after age 40 [23], compared with women aged 20–24, women over the age of 40 had a significantly increased risk of infertility in both the “first child intention” and “second child intention” groups. Due to physiological processes such as ovarian reserve and decreased sperm quality, fertility rapidly declines in this age group, which greatly increases the incidence of infertility [23, 24]. The incidence of infertility in Shanghai is currently almost double what it was in 2002 and exceeds the incidence of infertility in China [20]. This could be related to Shanghai's social, cultural, and economic development in the past 15 years [5]. Economic development has brought tremendous social progress and has caused people to pursue education, careers, and higher incomes, resulting in couples that do not become pregnant in early adulthood. Previous studies have suggested that it is best for women to become pregnant before they are 35 [25]. As females age, ovarian function declines, as does fertility [26]. Work stress and occupational exposure also affect women's endocrine function, which endangers fertility [27]. 95.27% of the women in this study had stable jobs. Due to increasing work pressure and hours worked by women in recent years, the resulting exhaustion and mental stress could promote the secretion of an adrenocortical hormone-releasing hormone. This interrupts the normal gonadal feedback in the brain, thereby affecting a series of conception processes and reducing the clinical pregnancy rate [28]. Similar to studies on infertility rates in other regions of China [9, 20], this study found that the annual infertility rate from 2013 to 2017 increased, especially after 2016, and ultimately reached 21.4%. This is most likely related to 2016 changes in the national population policy when the universal two-child policy was implemented, increasing the proportion of elderly and high-risk pregnant women [29]. Additionally, as mentioned above, the increasing work intensity in recent years has also increased infertility rates. Numerous studies have shown the effects of the female reproductive history and gynecological history on infertility [30, 31]. Our investigation confirmed that factors related to infertility for women included menstrual history (long menstrual cycle or long menstrual duration), gynecological history (leiomyoma, PCOS, endometrial polyps, or endometriosis), surgical history (salpingostomy), and infection history (chlamydia). Additionally, several researchers have explained the relationship between these risk factors and infertility, which could be related to ovulation disorders, deterioration of the intrauterine environment, and pathological changes in the cervix [32, 33]. The prevalence of infertility can be altered using various approaches. Primary infertility is commonly calculated by the DHS-type (Demographic and Health Survey) infertility measure [34], while some scholars have applied the novel current duration approach and calculated that the prevalence of infertility was two times higher than the traditionally constructed measure [35]. These studies emphasize that the definition and methodological methods are important when estimating the prevalence of infertility. Our study established a prospective cohort to obtain infertility incidence rates, focusing on the frequency of new infertility in a subset of the population while reducing recall bias. On the other hand, prevalence was assessed using cross-sectional studies that analyze the ratio of new and old disease cases in a population over a period of time. Therefore, the incidence of infertility and related risk factors obtained in this study have clinical importance. We conducted the first studies assessing the incidence and risk factors of infertility in couples seeking to have a first and second child. However, our study had some limitations. First, because male infertility factors were not fully covered, we did not identify any significant risk factors related to male infertility. Second, as the prospective cohort was established from a single institution, this study did not use the Probability Proportional to Size (PPS) sampling method; simple random sampling was used to recruit research objects. As proportional sampling methods, simple random sampling can ensure equal opportunities for each subject in the target population and effectively obtain representative samples in this study [36]. Although our sample was obtained from the community and the sampling method was effective, our cohort was based on a cohort established by pre-pregnancy centers, meaning there was some bias in how the overall population was represented. Finally, based on our analysis of infertility incidence rather than infertility prevalence, the study excluded infertile people at the inclusion stage. This could have produced differing research results, and particularly underestimated factors such as some gynecological diseases that affect infertility. Therefore, future research design should include more samples and an infertile population.

Conclusions

This survey showed that the infertility rate is approximately 16.95% in our sample. The incidence of infertility in the “first child intention” and “second child intention” groups was 19.30% and 4.14%, respectively. Our data also showed risk factors related to infertility in the “first child intention” and “second child intention” groups. However, some mechanisms leading to infertility are still unclear and require further study. To some extent, these results can inform government and medical institutions seeking to make policies governing population size. Age is an important risk factor for infertility, and couples who marry when they are older is an important factor affecting overall fertility. Medical workers can use their influence to inform couples of the benefits and drawbacks of having children at certain ages, while the government can strengthen fertility subsidies to couples of childbearing ages to increase fertility levels. Additional file 1: Table S1. Multi-collinearity analysis between independent variables included in the regression models.
  32 in total

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Journal:  Reprod Biomed Online       Date:  2014-10-13       Impact factor: 3.828

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Review 6.  Ovarian ageing: the role of mitochondria in oocytes and follicles.

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7.  The epidemiology of infertility in the North East of Scotland.

Authors:  S Bhattacharya; M Porter; E Amalraj; A Templeton; M Hamilton; A J Lee; J J Kurinczuk
Journal:  Hum Reprod       Date:  2009-08-14       Impact factor: 6.918

Review 8.  Tubal factor infertility: diagnosis and management in the era of assisted reproductive technology.

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Authors: 
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