{"paper_id":"302d5bef-d2e8-416a-a8cd-5515db8dfafc","body_text":"Female infertility is the inability of a woman of reproductive age to conceive without contraception with the same sexual partner for more than 1 year [ 1 ]. Some scholars believe that the prevalence of infertility is an “iceberg phenomenon” and that most couples with infertility remain undiagnosed [ 2 ]. Female infertility has a devastating impact on the physical and mental health of individuals and national fertility, resulting in a burden of medical costs [ 3 ]. The prevalence of infertility varies globally, affecting approximately 8–12% of couples of reproductive age [ 4 ].\nFemale infertility includes primary infertility, where the woman has not been pregnant without contraception with the same sexual partner for a minimum of 1 year, and secondary infertility, where the woman has not been pregnant without contraception with the same sexual partner for 12 months or more since the last pregnancy [ 5 ]. There are many causes of female infertility, including ovulation dysfunction, tubal blockage, endometriosis, uterine, and cervical causes [ 6 ]. The risk of infertility is heightened by other variables, including smoking, unsafe abortion, and sexually transmitted infections [ 7 ]. In addition, social factors such as exposure to toxic substances before/during pregnancy, delayed childbearing, poor socioeconomic status of women, intimate relationship violence, and sexually transmitted infections are important contributors to the reduction in female fertility [ 7 ].\nSun et al. [ 8 ] used the Global Health Data Exchange query tool to evaluate the regional, national, and global burden of infertility from 1990 to 2017. Additionally, from 1990 to 2019, Liu et al. [ 9 ] investigated the global disease burden associated with endometriosis-related primary and secondary infertility. Furthermore, many systematic studies related to female infertility have been published. However, most of these studies were conducted on rather small sample sizes and have certain limitations [ 10 – 12 ].\nTherefore, we evaluated the female infertility global burden between 1990 and 2019 in this systematic study based on the following criteria: prevalence, disability-adjusted life-years (DALYs), age-standardized prevalence rates (ASR), average annual percent change (APC), and a sociodemographic index (SDI; combining indicators of per capita income, years of schooling, and fertility) and assessed their relationship with levels of development. This study also discusses the related causes of female infertility, classified the causes according to primary and secondary infertility, and analyzed the proportion of each cause in female infertility.\n\nThe design and standardization procedures of global burden of disease (GBD) investigations have been extensively reported in existing GBD literature [ 13 – 15 ]. GBD 2019 provides a systematic and comprehensive evaluation of 369 diseases and injuries across 204 countries and territories, covering age- and sex-specific incidence, prevalence, years of life lost, DALYs, mortality, and years of disability, between 1990 and 2019.\nThe Global Health Data Exchange query tool ( http://ghdx.healthdata.org/gbd-results-tool ) and SDI ( http://ghdx.healthdata.org/data-type/estimate ) provided data on the annual prevalence numbers, ASRs, and DALYs of female infertility in 204 countries and territories from 1990 to 2019 for various age groups.\nThe GBD 2019 research uses the SDI, a composite indicator, to provide a summary of sociodemographic progress in a specific area [ 13 ]. The average personal income per capita, the education level of residents above the age of 15, and the total population fertility rate are used to compute the SDI. The SDI, which ranges from 0 to 1, is a comprehensive marker of geographical development based on national per capita income, average educational attainment, and total fertility. 204 countries and territories were divided into five levels according to SDI: low (0–0.455), medium-low (0.456–0.608), medium (0.609–0.690), medium-high (0.691–0.805), and high (0.806–1) SDI regions [ 16 ].\nThe burden of nonfatal diseases was modeled by GBD, employing the Bayesian meta-regression tool disMOd-MR 2.1. ASR, representing a weighted average of a specific age ratio, is calculated by aggregating measures of the ratio a population would have if it had a standard age structure. The standard population’s distribution is used to determine the weights using the following formula:  ASR = ∑ i = 1 A α i w i ∑ i = 1 A w i × 100 , 000 . The specific age ratio, denoted as  αi,  highlights the number (or weight) of the chosen standard population per 100,000 individuals. The linear regression line is fitted to the ASR-related natural logarithm to determine the estimated annual percentage change (EAPC): EAPC = ln (ASR) = α+β x +ε, the  x  signifies the calendar year, and the ε denotes the error term. The 95% confidence interval for ε is computed as follows: 100 × (exp(β) − 1) [ 17 ]. As the EAPC value and its 95% confidence interval rise above zero, the corresponding ASR trends upward, and vice versa [ 18 ]. A smoothed spline model was employed in this study to evaluate the relationship between women’s burden of infertility and SDI. The Spearman order correlation technique was used for correlation analysis, considering a value of  p  < 0.05 as statistically significant. R 4.3.1 was utilized (R Foundation, Vienna, Austria,  https://www.r-project.org/ ) for the analysis. Each step used to analyze the GBD database in this study complied with the cross-sectional study guidelines stipulated in the Guidelines for Accurate and Transparent Health Estimates Reporting [ 19 ].\n\nIn 2019, 122.38 million (95% uncertainty interval [UI]: 58.38–209.12) cases of female infertility were reported globally among women at reproductive age (20–49 years), with an increase of 86.36% (95% UI: 74.01–97.98%) from 1990 to 2019 in all ages (online suppl. Table 1; for all online suppl. material, see  https://doi.org/10.1159/000542408 ). The global ASR of infertility in reproductive-aged women was (3,089.18 [95% UI: 1,476.17–5,271.85] per 100,000 population) in 2019 ( Fig. 1 a), accounting for a rise of 23.97% (95% UI: 16.27–31.99%) compared with that in 1990 (online suppl. Table 1).\nTrends in global disease burden of female infertility prevalence from 1990 to 2019.  a  Trends in global disease burden of female infertility prevalence by SDI from 1990 to 2019.  b  Trends in global disease burden of female infertility prevalence by region from 1990 to 2019.\nThe total number of DALYs linked to female infertility was 0.66 (95% UI: 0.22–1.57) million globally in 2019, indicating an increase of 87.00% (95% UI: 74.93–99.39%) between 1990 and 2019 in all ages (online suppl. Table 1). In 2019, 16.65 (95% UI: 5.66–39.75) age-standardized DALYs per 100,000 women globally due to female infertility of reproductive years were reported ( Fig. 2 a), indicating an increase of 24.95% (95% UI: 17.07–32.82%) from 1990 to 2019 (online suppl. Table 1).\nTrends in global disease burden of female infertility DALYs from 1990 to 2019.  a  Trends in global disease burden of female infertility DALYs by sociodemographic index from 1990 to 2019.  b  Trends in global disease burden of female infertility DALYs by region from 1990 to 2019.\nAll SDI regions exhibited a growing trend when stratified by SDI quintiles. The ASR of middle-SDI and high-middle-SDI regions was consistently high from 1990 to 2019. GBD established seven super regions based on epidemiological similarity and geographic proximity, including “Southeast Asia, East Asia and Oceania,” “Southern Asia,” “North Africa and the Middle East,” “Sub-Saharan South Africa,” “Latin America and the Caribbean,” “Central and Eastern Europe” and “Central Asia.” However, among the seven super regions, regions with high-SDI recorded the lowest female infertility ASR. In 2019, the ASR of high-SDI region was (1,327.16 [95% UI: 470.52–2,609.23] per 100,000 population) ( Fig. 1 a), whereas the values for middle-SDI and high-middle-SDI regions were (3,498.50 [95% UI: 1,687.45–5,955.29])and (3,442.46 [95% UI: 1,628.77–5,789.99]), respectively ( Fig. 1 a).\nThe age-standardized DALYs rate per 100,000 women in high-SDI region was 7.37 (95% UI: 1.96–18.37) in 2019 ( Fig. 2 a). Middle SDI had the highest age-standardized DALYs rate (18.80 (95% UI: 6.41–45.04), per 100,000 population) in 2019 ( Fig. 2 a), followed by high-middle-SDI regions (18.41 (95% UI: 6.13–44.78) per 100,000 population) ( Fig. 2 a).\nThe percentage change in ASR of regions with high SDI (41.59% [95% UI: 24.82–56.32%]) increased significantly (online suppl. Table 1), ranking second among all SDI regions, with low-middle SDI exhibiting the highest increase (42.95% [95% UI: 24.53–68.54%]) (online suppl. Table 1). Conversely, the percentage change in ASR was lowest of regions with high-middle SDI (12.07% [95% UI: 5.52–18.34%]) (online suppl. Table 1).\nIn 2019, the highest age-standardized female infertility prevalence rates were observed in East Asia (4,922.57 [95% UI: 2,313.33–8,502.39] per 100,000 population), Eastern Europe (3,734.20 [95% UI: 1,844.37–6,311.99] per 100,000 population), and Southern Sub-Saharan Africa (3,636.60 [95% UI: 1,651.50–6,231.13] per 100,000 population) ( Fig. 1 b). Conversely, the lowest ASR was observed in Australasia (102.87 [95% UI: 31.40–429.00]) per 100,000 population), Andean Latin America (286.23 [95% UI: 51.66–793.09]) per 100,000 population), and high-income Asia Pacific (522.40 [95% UI: 53.18–1,622.97]) per 100,000 population). In addition, Andean Latin America and Australasia increased minimally from a very low base ( Fig. 1 b).\nThe percentage change in ASR declined between 1990 and 2019 in only two regions: high-income Asia Pacific (−12.24% [95% UI: −37.03–12.18%]), and Southern Latin America (−1.14% [95% UI: −21.32 to −16.95%]). Concurrently, the ASR in Andean Latin America (266.48% [95% UI: −12.51–908.62%]) and Western Sub-Saharan Africa (130.17% [95% UI: 60.80–196.57%]) had the steepest increases in the percentage change of age-standardized rate from 1990 to 2019, although the change in Andean Latin America was from a very low base. Similarly, Central Latin America, Tropical Latin America, high-income North America, South Asia, North Africa and Middle East also had obvious increase in percentage change from 1990 to 2019 (online suppl. Table 1).\nThe regions of East Asia (25.65 [95% UI: 8.29–62.94] per 100,000 population), Eastern Europe (20.85 [95% UI: 7.23–51.08] per 100,000 population), and Southern Sub-Saharan Africa (19.70 [95% UI: 6.69–47.71] per 100,000 population) had the highest age-standardized DALYs rates in 2019 ( Fig. 2 b), whereas Australasia (0.56 [95% UI: 0.12–2.53] per 100,000 population), Andean Latin America (1.53 [95% UI: 0.23–4.94]) per 100,000 population), and high-income Asia Pacific (2.71 [95% UI: 0.24–9.27]) per 100,000 population) had the lowest age-standardized DALYs rate ( Fig. 2 b).\nAndean Latin America (262.81% [95% UI: −6.54–849.37%]), Western Sub-Saharan Africa (128.62% [95% UI: 62.28–193.14%]), and Central Latin America (112.08% [95% UI: 71.56–168.61%]) had the steepest increases in the percentage change of age-standardized DALYs from 1990 to 2019, whereas high-income Asia Pacific (−12.54% [95% UI: −37.34 to 11.90%]) and Southern Latin America (−1.85% [95% UI: −23.69 to 14.46%]) exhibited the downward trend during this period. Similar to the results of ASR, the age-standardized DALYs rate in Andean Latin America was still very low in 2019 (online suppl. Table 1).\nFrom 1990 to 2019, the prevalence of female infertility among women of reproductive age (20–49 years) increased globally. Regarding prevalence across the ages of 20–49 years in 2019, the 30–34 years age group recorded the highest value at 30.66 (95% UI: 9.39–68.77) million, while the 45–49 years age group recorded the lowest value at 1.13 (95% UI: 0.07–5.56) million in 2019 (online suppl. Table 2;  Fig. 3 a). In addition, the prevalence in the 45–49 years age group remained relatively low from 1990 to 2019. In addition, the other age groups all recorded a rapid growth trend. The age groups of female infertility in DALYs showed similar results (online suppl. Table 2;  Fig. 3 b).\nTrends in global disease burden of female infertility prevalence and DALYs in age groups from 20 to 49 years old from 1990 to 2019.  a  Prevalence.  b  DALYs.\nThe following five countries ranked the highest in 2019 for the ASR of female infertility per 100,000 population: Central African Republic (5,847.42 [95% UI: 2,990.76–9,859.64]), Djibouti (5,558.83 [95% UI: 2,832.56–9,593.05]), the Philippines (5,308.07 [95% UI: 1,509.00–9,355.45]), China 4,968.91 (95% UI: 2,334.85–8,590.40), and Comoros 4,953.49 (95% UI: 2,674.50–8,229.69) (online suppl. Table 6). Conversely, the lowest ASR per 100,000 population in the same year was recorded in Australia (81.95 [95% UI: 28.92–360.62]), Peru (90.51 [95% UI: 42.87–215.45]), New Zealand (228.35 [95% UI: 45.00–934.96]), Denmark (282.08 [95% UI: 28.89–786.91]), and Singapore (326.08 [95% UI: 36.93–1,212.18]) (online suppl. Table 6).\nSignificant differences in the percentage changes in female infertility ASR were observed between 1990 and 2019, with the steepest rises in Ecuador (490.73% [95% UI: −21.94 to 1,982.25%]), Colombia (480.94% [95% UI: 93.05–1,724.34%]), and Togo (353.47% [95% UI: 43.42–1,189.32%]). The steepest decreases were observed in Pakistan (−88.52% [95% UI: −95.35 to −82.87%]), Malawi (−24.89% [95% UI: −71.13 to 44.39%]), and Burundi (−19.60% [95% UI: −75.95 to 69.22%]) (online suppl. Table 3;  Fig. 4 a).\nGlobal disease burden of female infertility prevalence in 204 countries and territories.  a  The percentage change in age-standardized prevalence of female infertility between 1990 and 2019.  b  The estimated annual percentage change (EAPC) of female infertility age-standardized prevalence from 1990 to 2019.\nAccording to age-standardized DALYs related to female infertility per 100,000 population, the five top-ranking countries in 2019 were Central African Republic (31.76 [95% UI: 11.72–74.22]), Djibouti (29.58 [95% UI: 10.51–69.93]), the Philippines (29.41 [95% UI: 7.67–70.17]), Comoros (27.95 [95% UI: 10.44–62.25]), and Gabon (25.99 [95% UI: 9.04–62.95])(online suppl. Table 6). Conversely, the lowest age-standardized DALYs rates per 100,000 individuals were recorded in Australia (0.45 [95% UI: 0.10–2.00]), Peru (0.52 [95% UI: 0.14–1.57]), New Zealand (1.24 [95% UI: 0.17–5.26]), Denmark (1.66 [95% UI: 0.16–5.61]), and Singapore (1.68 [95% UI: 0.15–6.81]) (online suppl. Table 6).\nEcuador (475.25% [95% UI: −17.24 to 1,962.27%]), Colombia (459.48% [95% UI: 104.60–1,681.85%]), and Togo (326.55% [95% UI: 43.09–1,081.42%]) recorded the sharpest increases in the percentage changes of the age-standardized DALYs between 1990 and 2019, with steepest decline recorded in Pakistan (−88.02% [95% UI: −95.28 to −81.41%]), Malawi (−25.89% [95% UI: −69.53 to 40.23%]), and Vietnam (−19.71% [95% UI: −53.21 to −1.68%]) (online suppl. Table 3). Online supplementary Table 4 and  Figure 4 b present the EAPC of female infertility ASR from 1990 to 2019. Ecuador had the highest EAPC value (1,108.18% [95% UI: 1,381.96–840.99%]), and Pakistan had the lowest (−1,302.52% [95% UI: −1,025.11 to −1,571.36%]) (online suppl. Table 4;  Fig. 4 b).\nThe data on the causes of infertility in the GBD 2019 database are not perfect, and we selected several of them for analysis and research. Infertility in women can be of two types: primary and secondary. Globally, between 1990 and 2019, secondary infertility accounted for a higher proportion of female infertility. In 2019, the highest proportion of secondary infertility in 21 regions was Western Sub-Saharan Africa, and East Asia, the highest proportion of secondary infertility in SDI regions was high-middle SDI. For primary infertility, we chose “polycystic ovarian syndrome, endometriosis, urogenital congenital anomalies, Turner syndrome, and Klinefelter syndrome,” of which the highest ASR in 2019 was polycystic ovarian syndrome (8,101.49% [3,953.49%–14550.96%]). For secondary infertility, we chose “polycystic ovarian syndrome, endometriosis, and maternal sepsis and other maternal infections,” of which the highest ASR in 2019 was polycystic ovarian syndrome (22,733.37% [13,503.66%–35737.41%]) ( Tables 1 ,  2 ,  Fig. 5 a–c).\nGlobal ranking of female primary infertility by causes\nGlobal ranking of female secondary infertility by causes\nFemale infertility age-standardized prevalence rate and its proportion by etiologies.  a  Primary infertility age-standardized prevalence rate and its proportion in different SDI regions and countries by etiologies in 1990 and 2019.  b  Secondary infertility age-standardized prevalence rate and its proportion in different countries and SDI regions by etiologies in 1990 and 2019.  c  The proportion of primary infertility and secondary infertility for female infertility in different SDI regions and geographical regions in 1990 and 2019.\nWe presented the relationships between the SDI levels and the estimations of the global burden of female infertility for each of the 21 GBD regions and global for all individual years between 1990 and 2019. General negative correlations were observed between the SDI level and burden estimates. The expected pattern is essentially a nonlinear, bimodal pattern, with the first peak occurring at approximately SDI = 0.4, the second peak at approximately SDI = 0.7, and the turning point between the two peaks at approximately SDI = 0.55. When SDI <0.4, burden estimates increased; when SDI >0.7, the estimated burden exhibited a clear downward trend. In addition, fluctuations were observed when 0.4 < SDI < 0.7 (online suppl. Table 5;  Fig. 6 a, b).\nCoevolution of age-standardized burden estimates with SDI and for GBD regions for female infertility from 1990 to 2019.  a  Prevalence.  b  DALYs. Colored lines show region values for age-standardized burden estimate rates. Each point in a line represents 1 year, starting in 1990 and ending in 2019. The black line represents the average expected relationship between SDI and burden estimate rates for female infertility based on values from each region in the 1990–2019 estimation period.\n\nThis study is based on GBD estimates and trends in the burden of female infertility in 204 countries and regions from 1990 to 2019. The findings indicate a global increase in ASRs of female infertility over the observation period, with the burden of female infertility increasing in all countries at the SDI quintile level and in all regions at the regional level. The increased prevalence of female infertility may be related to the delayed childbearing age, as well as the increased prevalence of mental disorders such as depression and anxiety in modern women [ 20 ,  21 ]. Ovarian reserve function declines in older women, female reproductive potential steadily declines with age, and fertility rates drop sharply in women over the age of 35 [ 22 ,  23 ]. Women over 35 experience a rapid reduction in fertility rates, with their reproductive capacity and their ovarian reserve function continuously declining with age [ 24 ]. Infertility in women is also linked to several physical and psychological conditions, including anxiety, depression, obsessive-compulsive disorders, and sleep disturbances. Mental health issues and female infertility are related, although the exact mechanism of the two is uncertain. Women with infertility have higher levels of psychological stress and are more prone to developing mental health problems. Additionally, mental disorders will increase the difficulty of pregnancy in women with infertility [ 21 ,  25 ].\nOur study revealed that from 1990 to 2019, the ASR of female infertility was consistently high in middle-SDI and high-middle-SDI regions, while high-SDI countries exhibited the lowest ASR of female infertility among all seven SDI countries, consistent with the findings of Sun et al. [ 8 ]. This may be related to lower infertility detection rates in countries with low SDI. The rate of female infertility has risen in low-SDI countries with economic progress. Differences in female infertility may be caused by differences in the distribution of factors, such as education, culture, race, economic conditions, women’s status, medical level, and social security system. Higher income and educational attainment are socioeconomic benefits linked to infertility and delayed childbirth in developed countries [ 26 ]. The increase in late marriages and late childbearing in developed countries may also be related to the significant increase in the percentage change in ASR observed in high-SDI countries in this study, although policy related to infertility in developed countries are superior to those in low- and upper-middle-income countries [ 27 ]. While the average age of conception in developing countries is low, infertility rates among women in developing countries are also exacerbated by the increase in environmental pollution unwanted pregnancies, unsafe abortions, and the limitations of medical standards [ 28 ]. Higher rates of reproductive tract tuberculosis and female smoking in developing countries can also increase female infertility prevalence [ 29 ,  30 ]. Furthermore, in countries with high fertility rates and insufficient health resources, infertility is often considered a secondary issue by the government [ 31 ]. These factors may be partly responsible for the largest age-standardized prevalence increases observed in low-middle-SDI countries in this study.\nThe highest ASR in 2019 was observed in East Asia and Eastern Europe, whereas the lowest ASR was observed in Australasia and Andean Latin America. Between 1990 and 2019, ASR decreased in only two regions: high-income Asia Pacific and Southern Latin America. Additionally, between 1990 and 2019, the ASR displayed the relatively obvious increasing trends in Andean Latin America and Western Sub-Saharan Africa, but the ASR in Andean Latin America was still at a very low level in 2019. Secondary infertility is relatively prevalent in Central/Eastern Europe and Central Asia, and this may be attributed to greater rates of abortions. In these regions, abortion rates declined between 1995 and 2003 but remained higher than the global average [ 32 ]. In countries with limited resources, secondary infertility is more prevalent [ 33 ]. As East Asia’s largest country, China has a 25% infertility prevalence among couples of childbearing age, and nearly half of the couples with infertility choose not to seek medical assistance [ 34 ]. The high rate of infertility in Central and Southern Africa has led to the region being referred to as an “infertility belt” [ 35 ]. Pelvic infections and Fallopian tube injury after abortion are the leading cause of infertility in women of childbearing age in Central and Southern Africa. Therefore, the elimination of unsafe abortion and the early detection and treatment of postabortion complications are extremely important [ 36 ]. Female infertility is a major risk factor for intimate partner violence in low- and middle-income countries [ 37 ]. The prevalence of ASR in high-income North America has been at a low level in the past 30 years, but it has increased significantly in the last 10 years, which may be related to the degree of economic development and people’s fertility intention.\nSocial and economic support policies for female infertility also have a notable role in promoting fertility recovery [ 27 ]. Developed countries such as the USA and Europe have relatively effective healthcare policies, but the specific policies vary greatly [ 38 ,  39 ]. Conversely, comparatively few medical protection policies for female infertility exist in several low- and middle-income countries [ 40 ].\nAmong the women, aged 20–49 years, with female infertility worldwide between 1990 and 2019, the 45–49 years age group had the fewest cases, maintaining a relatively stable situation. In addition, the growth of the 20–24 years age group was relatively stable, while other age groups exhibited a rapid growth trend. The 30–34 years age range represented the largest proportion of female infertility cases in 2019, closely followed by the 35–39 years age group. Women in the 45–49 years age group are at the end of their reproductive age, with significantly lower reproductive demand and fertility compared with other reproductive age groups. Therefore, the number of women in this age group was the lowest among all age groups, with no significant fluctuation. Since the 1970s, more women have been delaying childbearing due to increasing access to higher education, full-time employment, and improved contraceptive techniques. Assisted reproductive technologies have also prolonged reproductive life. Furthermore, some women overvalue their fertility, being unaware of the effects of advanced age on fertility or acknowledging the risks of old age but not perceiving them as imminent. Delayed childbearing is now a global phenomenon [ 41 ,  42 ]. Pregnant women aged between 30 and 39 years constitute the primary childbearing population after delayed childbearing. Since 1978, the number of first births in women aged 35–39 years in the USA has increased by an average of 2% per year [ 43 ]. Between 1971 and 2013, the average age of new mothers in Australia increased from 25.4 to 29.3 years [ 44 ]. According to a review of natural childbearing populations in developed countries, age-related losses in fertility rose from 4.5% at age 25 to 20% at the age of 38 [ 41 ]. Global data reveal that fertility rates have declined over time, with the steepest declines among young women and regions with higher income and education levels [ 45 ]. Research illustrates that first-time mothers aged 35 years and older have shorter intervals between their second pregnancies than mothers aged 20–29 years [ 46 ]. This is because some women are aware of the negative effects of old age, such as decreased fertility [ 47 ]. Conversely, excessively lengthy or short gestation intervals are linked to a higher risk of unfavorable pregnancy outcomes, such as a fetus small for gestational age, low birth weight, and premature birth [ 48 ]. Additionally, some types of cancer, metabolic diseases, congenital abnormalities, and chromosomal diseases are more common in older mothers, who also have a higher annual morbidity of their children [ 49 ].\nIn addition to the etiology of infertility included in this study, many factors affect the prevalence of infertility, such as thyroid disease, pituitary disease, adrenal hyperplasia, or adrenal tumors caused by androgen elevation [ 50 ]. Several review articles offer reliable proof that abnormal sleep patterns are linked to several detrimental effects on women’s reproductive health; however, further research is required [ 51 ,  52 ]. A North American cohort study revealed that difficulty sleeping at night was linked to moderately reduced fertility, although the negative association between shorter sleep duration and fertility was weak, and shift work or a night job was not associated with fertility [ 53 ]. Obesity is also considered to be a cause of infertility. Obesity can have an adverse effect on embryo implantation [ 54 ]. Additionally, infertility raises the risk of ovarian, endometrial, and breast cancers; however, whether fertility treatment itself elevates these risks is uncertain [ 55 ].\nFrom the above research results, it is not difficult to see that the global infertility burden is still very severe and the overall trend is rising. This suggests that we must pay attention to this disease. We should call on patients to actively seek treatment, and the clinicians should improve the diagnosis and treatment system, strive to achieve early detection and early treatment. From the perspective of policymakers, they should improve the medical and health security system and reduce the economic concerns of patients seeking medical treatment. We believe that with the efforts of all sectors of society, the disease of female infertility will be better controlled, and the life treatment of patients will also be improved to a certain extent.\nThis study has a few limitations. First, the GBD database lacks data for some countries and regions. Second, data access and quality differ across locations. In some developing countries, women with infertility have low consultation rates, which lead to scarce or missing data, leading to bias in study results. Third, the causes of infertility are not comprehensive, and data on Klinefelter syndrome in GBD 2019 in relation to primary infertility were absent. Nevertheless, this study is the most recent in-depth analysis of the epidemiological state and trends of the global burden of female infertility, lending it considerable unique advantages.\nIn conclusion, from 1990 to 2019, the ASR of female infertility and DALYs increased globally. These increases may be related to various factors such as population aging, delayed childbearing, socioeconomic development, access to healthcare, and health awareness. This report presents comprehensive findings on the global burden of female infertility and can inform policymakers on healthcare priorities related to infertility, strengthening education, raising public awareness of female infertility, regulating intimate relationship violence, safeguarding the status and safety of women, and implementing necessary prevention and management interventions, to reduce the prevalence of female infertility.\n\nWe highly appreciate the works of the Global Burden of Disease Study 2019 collaborators. We thank Bullet Edits Limited for the linguistic editing and proofreading of the manuscript.\n\nThe data in this study are from the GBD open database, the informed consent waiver for the GBD 2019 data was reviewed and approved by the Institutional Review Board of the University of Washington.\n\nThe authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.\n\nThis study was supported by the National Nature Science Foundation of China (No. 82274571), the Shanghai Medical Innovation, and Development Foundation (WL-HBMS-2021004K).\n\nD.Y.S. wrote the original manuscript and conceived the study; S.Y. performed the data analysis; D.Y.S. and S.Y. revised the final manuscript; C.Q. and H.Y. supervised the study process.","source_license":"CC-BY-4.0","license_restricted":false}