Literature DB >> 34220704

Association Between Pre-Pregnancy Body Mass Index and Miscarriage in an Assisted Reproductive Technology Population: A 10-Year Cohort Study.

Pengfei Qu1,2, Mingxin Yan3, Doudou Zhao1, Dongyang Wang1, Shaonong Dang3, Wenhao Shi1,4, Juanzi Shi1,4, Chunli Zhang5.   

Abstract

Objective: To investigate the association between pre-pregnancy body mass index (BMI) and miscarriages in women who required assisted reproductive technology (ART) for conception.
Methods: A retrospective cohort study was conducted using a 10-year (2006-2015) sample of 14,994 pregnancy cycles with ART treatment in Northwest Women's and Children's Hospital, Xi'an, China. The effects of women's BMI before pregnancy on early miscarriage and miscarriage were assessed using generalized estimating equation models.
Results: The risks of early miscarriage and miscarriage were higher in the obese group than in the normal weight group [early miscarriage: relative risk (RR) = 1.36, confidence interval (CI): 1.12-1.65; miscarriage: RR = 1.40, 95% CI: 1.17-1.68]. Pre-pregnancy underweight was not associated with an increased risk of early miscarriage or miscarriage. We observed interactions between pre-pregnancy BMI and singleton or twin pregnancy in early miscarriage and miscarriage (P = 0.017 and P = 0.003, respectively). Twin pregnancy increased the effects of pre-pregnancy BMI on early miscarriage and miscarriage (early miscarriage: a. singleton pregnancy: RR = 1.02, 95% CI: 1.01-1.04; b. twin pregnancy: RR = 1.08, 95% CI: 1.03-1.13; miscarriage: a. singleton pregnancy: RR = 1.02, 95% CI: 1.01-1.04; b. twin pregnancy: RR = 1.08, 95% CI: 1.05-1.13). Conclusions: Pre-pregnancy obesity was associated with higher risks of early miscarriage and miscarriage in the ART population, and twin pregnancy increased the effects of pre-pregnancy BMI on early miscarriage and miscarriage. Women should maintain a normal BMI before ART initiation to prevent adverse pregnancy outcomes.
Copyright © 2021 Qu, Yan, Zhao, Wang, Dang, Shi, Shi and Zhang.

Entities:  

Keywords:  assisted reproductive technology; body mass index; miscarriage; obesity; twin pregnancy

Mesh:

Year:  2021        PMID: 34220704      PMCID: PMC8242335          DOI: 10.3389/fendo.2021.646162

Source DB:  PubMed          Journal:  Front Endocrinol (Lausanne)        ISSN: 1664-2392            Impact factor:   5.555


Introduction

In the past 40 years, assisted reproductive technologies (ART) have become a common option for infertile couples worldwide (1). It is estimated that eight million individuals have been conceived using ART (2). Compared with spontaneous conception, ART is associated with an increased risk of multiple gestations, miscarriage, congenital malformations, and preterm birth (3–6). The prevalence of overweight and obesity has increased in an alarming way in the past 50 years worldwide, and more than 39% of the adult population worldwide is now classified as overweight or obese (7, 8). With its economic development, diet, and lifestyle change, the prevalence of overweight and obesity in China is gradually reaching that in developed countries (9, 10). The prevalence of overweight or obesity in adults has increased from 22.8% to 30.1% between 2002 and 2012 in China (11). Pre-pregnancy BMI is an important indicator of pregnancy outcomes (12, 13). Nevertheless, studies on the associations between pre-pregnancy BMI and miscarriages are limited, and the conclusions are inconsistent for pregnant women receiving ART treatment (14–18). Although some studies have reported that pre-pregnancy underweight and obesity both increase the miscarriage rate of pregnant women receiving ART treatment (19, 20), other studies have reported no adverse effects of pre-pregnancy underweight, overweight, or obesity on the miscarriage rate of ART (14, 18). Thus, the objective of the present study was to analyze the influence of pre-pregnancy BMI on miscarriage in women receiving ART treatment. In total, 10 years of patient records, including demographic characteristics, ART treatments, and pregnancy outcomes, were collected and used to compare early miscarriage and miscarriage among different BMI groups in a single ART center in Xi’an, Shaanxi Province, Northwest China.

Materials and Methods

Study Design and Population

A retrospective cohort study was conducted using 10 years of clinical data (2006–2015) from the ART center at Northwest Women’s and Children’s Hospital, Northwest China. A total of 15,254 pregnancy cycles were conceived with in vitro fertilization (IVF)/intracytoplasmic sperm injection (ICSI) treatment. Consequently, 44 pregnancy cycles with missing pre-pregnancy BMI and 216 pregnancy cycles with missing covariates were excluded, leaving a total of 14,994 pregnancy cycles enrolled in this study ( ).
Figure 1

Eligibility assessment with exclusion criteria.

Eligibility assessment with exclusion criteria. Shaanxi Province requires that pregnancy outcomes (including early miscarriage and miscarriage) be reported in the Shaanxi Assisted Reproduction Database. In this study, all pregnancy outcomes were collected from the Assisted Reproduction Database. Demographic data and ART treatment data were collected and assessed by each patient’s clinician.

BMI Assessment

Weight (nearest 100 g) and height (nearest 1 cm) were measured and recorded by a trained nurse one month before ART treatment. BMI was calculated as weight/height2 (kg/m2). Based on the Chinese criteria (21), pregnant women were divided into four BMI groups: underweight (BMI < 18.5 kg/m2), normal weight (18.5 ≤ BMI < 24.00 kg/m2), overweight (24 ≤ BMI < 28.00 kg/m2), and obese (BMI ≥ 28 kg/m2). Based on the World Health Organization (WHO) criteria (22), pregnant women were divided into four BMI groups: underweight (BMI < 18.5 kg/m2), normal weight (18.5 ≤ BMI < 25.00 kg/m2), overweight (25 ≤ BMI < 30.00 kg/m2), and obese (BMI ≥ 30 kg/m2).

Definitions of Pregnancy Outcomes

Clinical pregnancy was confirmed using ultrasound at 26 days after blastocyst transfer or 28 days after cleavage-stage embryo transfer. Singleton and twin pregnancies were confirmed using ultrasonographic visualization of the gestational sacs and fetal heart. Early miscarriage and miscarriage were the primary outcome measures in this study. Early miscarriage was defined as the loss of pregnancy before 12 weeks of gestation. Miscarriage was defined as the loss of pregnancy before 20 weeks of gestation.

Confounding Variables

Based on the literature (23), potential factors correlated to pregnancy outcomes, such as patient baseline demographic characteristics, clinical characteristics, and treatment procedure, were also collected for the study participants. These included maternal age, smoking history (yes or no), gravidity (0, 1–2 and ≥3), parity (0 or ≥1), main etiology of infertility (tubal factor, ovarian factor, male factor, and other reasons), year of transfer (2006–2009, 2010–2012, and 2013–2015), sperm donation (yes or no), fertilization method (ICSI, IVF, and IVF + ICSI), fresh/frozen embryo transfer, blastocyst/cleavage-stage transfer, assisted hatching (yes or no), antral follicle count, basal serum follicle stimulating hormone (FSH) level, endometrial thickness, number of embryos transferred (1, 2, or ≥3), and singleton or twin pregnancy.

Statistical Analysis

The participants’ baseline characteristics are summarized using mean and standard deviation for normally distributed continuous variables, median and interquartile range (IQR) for non-normally distributed continuous variables, and counts and proportions for categorical variables. The chi-squared test or Fisher’s exact test was performed to compare categorical variables. Analysis of covariance and the Kruskal–Wallis test were performed to compare normally distributed variables and non-normally distributed variables, respectively. Generalized estimating equation (GEE) models with log link were employed to analyze the relationships between pre-pregnancy BMI and miscarriages, and in the same woman as a cluster effect. All multivariate analyses were adjusted for all baseline covariates (age, smoking history, gravidity, parity, main etiology of infertility, year of transfer, sperm donation, fertilization method, fresh/frozen embryo transfer, blastocyst/cleavage-stage transfer, assisted hatching, antral follicle count, basal serum FSH level, endometrial thickness, number of embryos transferred, and singleton or twin pregnancy). In the subgroup analysis, we explored the relationships between pre-pregnancy BMI and miscarriages in the subgroup of singleton and twin pregnancies. We conducted a sensitivity analysis using the BMI criteria proposed by the WHO. We also used restricted cubic splines to flexibly model the association between pre-pregnancy BMI and miscarriages. Statistical analyses were performed using the SAS software package (version 9.4; SAS Institute Inc., Cary, NC, USA). All P-values were two-sided with a significance level of < 0.05.

Results

Participants’ Characteristics

A total of 13,828 pregnant women who underwent ART and 14,994 pregnancy cycles were analyzed in the study. Pregnant women and pregnancy cycles were divided into underweight, normal weight, overweight, and obese groups according to the Chinese criteria. The patients’ mean age was 29.79 ± 4.08 years; 9,892 pregnancy cycles (65.97%) were embryos transferred between 2013 and 2015 and 10,699 (71.36%) were IVF treatment. The characteristics of participants are presented in . The overweight and obese groups were older and more likely to have higher gravidity and parity, higher antral follicle count, greater endometrial thickness, ovarian cause of infertility, and blastocyst transfer. Finally, the overweight and obese groups were more likely to have lower FSH levels, less sperm donation, and less ICSI treatment.
Table 1

Patient and cycle characteristics in ART pregnancies.

UnderweightNormal weightOverweightObese χ2/F value P value
Patient characteristics
Patient number130494092571544
Frequency of ART pregnancy, n (%)
 11211 (92.87)8646 (91.89)2370 (92.18)493 (90.63)2.9940.393
 ≥ 293 (7.13)763 (8.11)201 (7.82)51 (9.38)
Age (year), mean ± SD28.63 ± 3.7329.76 ± 4.0330.35 ± 4.2530.42 ± 4.18161.362<0.001 a
Smoking history, n (%)
 Yes2 (0.15)30 (0.32)10 (0.39)5 (0.92)6.0510.091b
 No1302 (99.85)9379 (99.68)2561 (99.61)539 (99.08)
Gravidity, n (%)
 0863 (66.18)5485 (58.30)1433 (55.74)314 (57.72)
 1-2376 (28.83)3202 (34.03)902 (35.08)190 (34.93)47.656<0.001
 ≥365 (4.98)722 (7.67)236 (9.18)40 (7.35)
Parity, n (%)
 01234 (94.63)8599 (91.39)2268 (88.21)488 (89.71)48.393<0.001
 ≥170 (5.37)810 (8.61)303 (11.79)56 (10.29)
Main etiology of infertility, n (%)
 Tubal factor566 (43.40)4576 (48.53)1252 (48.70)235 (43.20)169.889<0.001
 Ovarian factor40 (3.07)369 (3.92)209 (8.13)64 (11.76)
 Male factor285 (21.86)1875 (19.93)419 (16.30)97 (17.83)
 Other reasons413 (31.67)2589 (27.52)691 (26.88)148 (27.21)
Pregnancy cycle characteristics
Number of ART pregnancy cycles1397101962804597
Year of transfer, n (%)
 2006–2009131 (9.34)813 (7.94)150 (5.35)25 (4.19)
 2010–2012375 (26.84)2804 (27.50)685 (24.43)119 (19.93)74.699<0.001
 2013–2015891 (63.78)6579 (64.53)1969 (70.22)453 (75.88)
Sperm donation
 Yes134 (9.59)672 (6.59)138 (4.92)24 (4.02)39.854<0.001
 No1263 (90.41)9524 (93.41)2666 (95.08)573 (95.98)
Fertilization method, n (%)
 ICSI429 (30.71)2706 (26.54)675 (24.07)140 (23.45)
 IVF945 (67.64)7262 (71.22)2054 (73.25)438 (73.47)28.618<0.001
 IVF + ICSI23 (1.65)228 (2.24)75 (2.67)19 (3.18)
Timing of embryo transfer, n (%)
 Fresh embryo transfer790 (56.55)5914 (58.00)1588 (56.63)339 (56.78)2.5360.469
 Frozen embryo transfer607 (43.45)4282 (42.00)1216 (43.37)258 (43.22)
Day 3 or 5, n (%)
 Cleavage stage transfer925 (66.21)6730 (66.01)1731 (61.73)351 (58.79)28.655<0.001
 Blastocyst transfer472 (33.79)3466 (33.99)1073 (38.27)246 (41.21)
Assisted hatching, n (%)
 Yes381 (27.27)2902 (28.46)809 (28.85)158 (26.47)2.2520.522
 No1016 (72.73)7294 (74.54)1995 (71.15)439 (73.53)
Antral follicle count, Median (IQR)12 (9, 16)12 (9, 16)13 (10, 18)14 (10, 20)81.749<0.001 a
Basal serum FSH level (U/L), Median (IQR)7.05 (5.99, 8.18)6.54 (5.58, 7.75)6.31 (5.36, 7.35)6.06 (5.20, 7.07)216.551<0.001 a
Endometrial thickness (mm), median (IQR)10.40 (9.20, 11.80)10.50 (9.20, 12.00)10.50 (9.20, 12.10)10.80 (9.40, 12.20)13.7130.003 a
No. of embryos transferred, n (%)
 1230 (16.46)1585 (15.54)501 (17.87)94 (15.75)
 21064 (76.16)7769 (76.20)2076 (74.04)468 (78.39)14.3570.026
 ≥3103 (7.37)842 (8.26)227 (8.10)35 (5.86)
Singleton or twin pregnancy, n (%)
 singleton950 (68.00)7003 (68.68)1966 (70.11)409 (68.51)2.7150.438
 twin c447 (32.00)3193 (31.32)838 (29.86)188 (31.49)

aKruskal-Wallis test; bFisher exact test; cTwin pregnancy included 93 triplet pregnancies.

IQR, interquartile range.

Patient and cycle characteristics in ART pregnancies. aKruskal-Wallis test; bFisher exact test; cTwin pregnancy included 93 triplet pregnancies. IQR, interquartile range.

BMI and Early Miscarriage

Overall, the rate of early miscarriage was 11.87% among all pregnancy cycles. The rates of early miscarriage varied according to pre-pregnancy BMI. Among the underweight, normal weight, overweight, and obese groups, the rates of early miscarriage were 10.67%, 11.44%, 13.20%, and 15.91% (P < 0.001), respectively (see for details).
Table 2

Relationship between miscarriage and pre-pregnancy BMI in ART pregnancies.

Pregnancy outcomesTotal (n = 14994)Underweight (n=1397)Normal weight (n=10196)Overweight (n=2804)Obese (n=597) χ2 value P value
Early miscarriage (<12 weeks), n (%)1780 (11.87)149 (10.67)1166 (11.44)370 (13.20)95 (15.91)17.809< 0.001
Miscarriage (<20 weeks), n (%)1932 (12.89)155 (11.10)1269 (12.45)401 (14.30)107 (17.92)24.244< 0.001
Relationship between miscarriage and pre-pregnancy BMI in ART pregnancies. After adjusting for baseline covariates (age, smoking history, gravidity, parity, etiology of infertility, and year of transfer), the obesity group had a 32% increased risk of early miscarriage relative to the normal weight group (relative risk [RR] = 1.32, 95% confidence interval [CI]: 1.08–1.61). After adjusting for all baseline covariates, this association remained statistically significant (RR = 1.36, 95% CI: 1.12–1.65). Additionally, after adjusting for all baseline covariates, for a one-unit increment of pre-pregnancy BMI, the RR of early miscarriage increased by 3% (RR = 1.03, 95% CI: 1.01–1.04) (see for details).
Table 3

Effects of pre-pregnancy BMI on miscarriage: results from the GEE models analysis.

Pregnancy outcomesModel 1Model 2Model 3
Crude RR (95% CI), P valueAdjusted RR (95% CI), P valueAdjusted RR (95% CI), P value
Early miscarriage
 Underweight0.93 (0.79–1.09), 0.3941.00 (0.85–1.17), 0.9750.99 (0.84, 1.16), 0.877
 Normal weightRefRefRef
 Overweight1.15 (1.03–1.29), 0.0131.11 (0.99–1.24), 0.0721.11 (0.99, 1.24), 0.064
 Obese1.39 (1.14–1.70), 0.0011.32 (1.08–1.61), 0.0061.36 (1.12, 1.65), 0.002
Early miscarriage
 BMI1.03 (1.02–1.05), < 0.0011.02 (1.01–1.04), 0.0011.03 (1.01, 1.04), < 0.001
Miscarriage
 Underweight0.89 (0.76–1.04), 0.1490.95 (0.81–1.11), 0.5380.94 (0.81, 1.10), 0.466
 Normal weightRefRef
 Overweight1.15 (1.03–1.28), 0.0111.10 (0.99–1.23), 0.0751.10 (0.99, 1.22), 0.071
 Obese1.44 (1.20–1.73), < 0.0011.36 (1.13–1.64), 0.0011.40 (1.17, 1.68), < 0.001
Miscarriage
 BMI1.04 (1.02–1.05), < 0.0011.03 (1.01–1.04), < 0.0011.03 (1.02, 1.04), < 0.001

Model 2 adjusted age, smoking history, gravidity, parity, etiology of infertility, year of transfer.

Model 3 adjusted all baseline covariates (age, smoking history, gravidity, parity, etiology of infertility, year of transfer, sperm donation, fertilization method, frozen or fresh embryo transfer, cleavage stage or blastocyst transfer, assisted hatching, antral follicle count, basal serum FSH, endometrial thickness, no. of embryos transferred, and singleton or twin pregnancy).

Effects of pre-pregnancy BMI on miscarriage: results from the GEE models analysis. Model 2 adjusted age, smoking history, gravidity, parity, etiology of infertility, year of transfer. Model 3 adjusted all baseline covariates (age, smoking history, gravidity, parity, etiology of infertility, year of transfer, sperm donation, fertilization method, frozen or fresh embryo transfer, cleavage stage or blastocyst transfer, assisted hatching, antral follicle count, basal serum FSH, endometrial thickness, no. of embryos transferred, and singleton or twin pregnancy).

BMI and Miscarriage

Overall, the rate of miscarriage was 12.89% among all pregnancy cycles. The rates of miscarriage varied according to pre-pregnancy BMI. Among the underweight, normal weight, overweight, and obese groups, the rates of miscarriage were 11.10%, 12.45%, 14.30%, and 17.92% (P < 0.001), respectively (see for details). After adjusting for baseline covariates (age, smoking history, gravidity, parity, and etiology of infertility, year of transfer), the obesity group had a 36% increased risk of miscarriage, compared with the normal weight group (RR = 1.36, 95% CI: 1.13–1.64). After adjusting for all baseline covariates, this association remained statistically significant (RR = 1.40, 95% CI: 1.17–1.68). Additionally, after adjusting for all baseline covariates, with a one-unit increment of pre-pregnancy BMI, the RR of miscarriage increased by 3% (RR = 1.03, 95% CI: 1.02–1.04) (see for details).

Subgroup Analyses

Subgroup analyses of the relationship between pre-pregnancy BMI and miscarriage were performed by singleton and twin pregnancies (see for details). The RRs of early miscarriage and miscarriage were significantly elevated with increased BMI for both singleton pregnancy and twin pregnancy groups. Increased pre-pregnancy BMI was associated with higher RRs of early miscarriage and miscarriage in the twin pregnancy group than in the singleton pregnancy group [early miscarriage (singleton pregnancy: RR = 1.02, 95% CI: 1.01–1.04; twin pregnancy: RR = 1.08, 95% CI: 1.03–1.13); miscarriage (singleton pregnancy: RR = 1.02, 95% CI: 1.01–1.04; twin pregnancy: RR = 1.08, 95% CI: 1.05–1.13)]. Tests of the interaction between pre-pregnancy BMI and singleton pregnancy or twin pregnancy in early miscarriage and miscarriage were statistically significant (P = 0.017 and P = 0.003, respectively).
Table 4

Effects of pre-pregnancy BMI on miscarriage: results from the GEE models analysis in subgroups.

Pregnancy outcomesSingleton pregnancy Twin pregnancy P for interaction
TotalEvents Adjusted RR (95% CI), P valuea TotalEventsAdjusted RR (95% CI),P valuea
Early miscarriage
 Underweight950138 (14.53)1.02 (0.86–1.20), 0.84844711 (2.46)0.79 (0.43–1.45), 0.452
 Normal weight70031060 (15.14)Ref3193106 (3.32)Ref0.018
 Overweight or obese2375321 (16.33)1.08 (0.97–1.21), 0.145102662 (6.04)1.70 (1.25–2.32), < 0.001
Early miscarriage
 BMI103281601 (15.50)1.02 (1.01–1.04), 0.0074666179 (3.84)1.08 (1.03–1.13), 0.0010.017
Miscarriage
 Underweight950142 (14.95)0.99 (0.84–1.16), 0.86844713 (2.91)0.68 (0.39–1.19), 0.174
 Normal weight70031126 (16.08)Ref3193143 (4.48)Ref0.005
 Overweight or obese2375427 (17.98)1.08 (0.97–1.19), 0.163102681 (7.89)1.68 (1.29–2.19), < 0.001
Miscarriage
 BMI103281695 (16.41)1.02 (1.01–1.04), 0.0034666237 (5.08)1.08 (1.05–1.13), < 0.0010.003

Model adjusted by age, smoking history, gravidity, parity, etiology of infertility, year of transfer.

Effects of pre-pregnancy BMI on miscarriage: results from the GEE models analysis in subgroups. Model adjusted by age, smoking history, gravidity, parity, etiology of infertility, year of transfer. Overweight or obesity was associated with higher RRs of early miscarriage and miscarriage in the twin pregnancy group (early miscarriage: RR = 1.70, 95% CI: 1.25–2.32; miscarriage: RR = 1.68, 95% CI: 1.29–2.19); however, overweight or obesity was not significantly associated with higher RRs of early miscarriage or miscarriage in the singleton pregnancy group (early miscarriage: RR = 1.08, 95% CI: 0.97–1.21; miscarriage: RR = 1.08, 95% CI: 0.97–1.19). Moreover, the tests of the interaction between the pre-pregnancy BMI and singleton pregnancy or twin pregnancy in early miscarriage and miscarriage were statistically significant (P = 0.018 and P = 0.005, respectively).

Sensitivity Analyses

Based on the BMI criteria proposed by the WHO, obesity was associated with an increased risk of early miscarriage and miscarriage relative to the normal weight group (early miscarriage: RR = 1.43, 95% CI: 1.09–1.90; miscarriage: RR = 1.48, 95% CI: 1.13–1.95). We also found that being overweight was associated with an increased risk of early miscarriage and miscarriage relative to the normal weight group (early miscarriage: RR = 1.19, 95% CI: 1.06–1.35; miscarriage: RR = 1.19, 95% CI: 1.06–1.34) (see ). As shown in , the results of restricted cubic splines revealed that the risk of early miscarriage and miscarriage was relatively flat until a BMI of approximately 24 kg/m2 and then started to increase rapidly afterward.
Figure 2

Association of pre-pregnancy BMI with early miscarriage (A) and miscarriage (B). Estimates adjusted for age, smoking history, gravidity, parity, etiology of infertility, year of transfer, sperm donation, fertilization method, frozen or fresh embryo transfer, cleavage stage or blastocyst transfer, assisted hatching, antral follicle count, basal serum FSH, endometrial thickness, no. of embryos transferred, and singleton or twin pregnancy. OR, odds ratio.

Association of pre-pregnancy BMI with early miscarriage (A) and miscarriage (B). Estimates adjusted for age, smoking history, gravidity, parity, etiology of infertility, year of transfer, sperm donation, fertilization method, frozen or fresh embryo transfer, cleavage stage or blastocyst transfer, assisted hatching, antral follicle count, basal serum FSH, endometrial thickness, no. of embryos transferred, and singleton or twin pregnancy. OR, odds ratio.

Discussion

In a large cohort of pregnant women undergoing ART treatment, we found that pre-pregnancy obesity was associated with a higher risk of early miscarriage and miscarriage, whereas pre-pregnancy underweight was not associated with an increased risk of early miscarriage and miscarriage. Additionally, we found interactions between pre-pregnancy BMI and singleton or twin pregnancy in the risk of early miscarriage and miscarriage. Twin pregnancy increased the RR of increased pre-pregnancy BMI in early miscarriage and miscarriage. In our study, the obese group had 36% and 40% increased risk of early miscarriage and miscarriage, respectively, compared with the normal weight group. In spontaneous pregnancies, pre-pregnancy obesity is a known risk factor for pregnancy complications and adverse perinatal outcomes (24–26). Balsell et al. conducted a meta-analysis that included 32 studies with a total of 265,760 women, and reported that pre-pregnancy obesity increased the risk of miscarriage in subgroups of the cohort study and case control study (RR = 1.21, 95% CI: 1.15–1.27; odds ratio [OR] = 1.26, 95% CI: 1.01–1.57) (16). In related ART studies, Kawwass et al. confirmed that pre-pregnancy obesity was associated with increased risk of miscarriage (RR = 1.23, 95% CI: 1.20–1.26) (27). Additionally, Metwally et al. conducted a meta-analysis that included 16 studies with more than 16,000 participants, and the results revealed that BMI ≥ 25 kg/m2 increased the risk of miscarriage (OR = 1.67, 95% CI: 1.25–2.25), and overweight or obesity was associated with a higher risk of miscarriage in the oocyte donation and ovulation induction groups (OR = 1.52, 95% CI: 1.10–2.09; OR = 5.11, 95% CI: 1.76–14.83); this trend was also seen in the IVF/ICSI group, but the association was not statistically significant (OR = 1.52, 95% CI: 0.88–2.61) (28). Several mechanisms have been proposed to explain the association between pre-pregnancy obesity and miscarriage. First, the association between increased BMI and increased risk of miscarriage might be related to the action of leptin produced in the adipose tissue (29, 30). Leptin receptors are expressed in the secretory endometrium and regulate endometrial angiogenesis (31), and thus may influence implantation (29, 30). Second, a high BMI has been confirmed to be associated with insulin resistance. Insulin resistance increases the risk of miscarriage both after natural conception (32) and and ART treatment (33). Insulin resistance involved in miscarriage is related to diminished endometrial production of adhesion factors, such as insulin-like growth factor (34–36). Additionally, obesity is associated with reduction in serum progesterone level in early pregnancy (37–39), which is essential for maintaining pregnancy and predicting subsequent pregnancy loss (40). In our study, compared with women with pre-pregnancy normal weight, women with pre-pregnancy underweight had a similar chance of miscarriage after ART treatment. A large sample of 180,855 ART pregnancies in the USA also confirmed that underweight was not significantly associated with increased miscarriage (RR = 1.04, 95% CI: 0.98–1.11) (27). However, other studies have drawn contrasting conclusions. Veleva et al. used 3,330 first pregnancy cycles conceived through IVF/ICSI and frozen-thawed embryo transfer, and Cai et al. used 4,798 first fresh transfer cycles, conceived through IVF, to explore the association between low BMI and miscarriage, and reported that low BMI was associated with an increased risk of miscarriage in ART treatment (19, 20). The inconsistent conclusions might be due to the relatively small sample size of the underweight group in Veleva et al.’s and Cai et al.’s studies, which might lack sufficient statistical power. Additionally, Veleva et al. and Cai et al. only analyzed the first pregnancy cycle, while our study used all pregnancy cycles to explore the association between BMI and miscarriages. In our subgroup analysis and sensitivity analysis, pre-pregnancy underweight was not associated with an increased risk of early miscarriage and miscarriage with ART treatment. We found interactions between pre-pregnancy BMI and singleton pregnancy or twin pregnancy in early miscarriage and miscarriage. Although miscarriage rates were higher in the singleton pregnancy group than in the twin pregnancy group, increased BMI was associated with a higher RR of early miscarriage and miscarriage in the twin pregnancy group than in the singleton pregnancy group. In ART treatment, twin pregnancies are mainly due to the transfer of multiple embryos (two or three embryos) related to lower reproductive capability, such as advanced age, poor uterine receptivity, and low-grade embryo quality (41). Pre-pregnancy obesity has been recognized as a major risk factor for adverse maternal outcomes, including hypertensive disorders and glucose intolerance (42). Women with twins are at an increased risk for many of the complications associated with maternal obesity described above, which may be related to an increased risk of miscarriage. The results of our study demonstrated that efforts should be devoted to the management of anthropometric parameters before ART treatment to prevent adverse pregnancy outcomes. In this study, in contrast to other large studies on the relationship between BMI and pregnancy outcomes, we found interactions between maternal BMI and singleton or twin pregnancy with respect to miscarriage in ART treatment. Moreover, we confirmed that obesity increased the risk of early miscarriage and miscarriage after ART treatment. Additionally, overweight and obesity were classified according to the Chinese standard, which is more applicable in Chinese adults than the WHO standard. This study has some limitations. First, this was an observational study in which the causality between BMI and miscarriages could not be established. Additionally, although we used multivariable regressions to control for potential confounders, the findings might be confounded by unmeasured covariates (e.g., alcohol consumption during pregnancy and maternal nutritional status) because the data in hospital information systems were limited.

Conclusion

In conclusion, our findings indicate that pre-pregnancy obesity is associated with an increased risk of early miscarriage and miscarriage in a population that underwent ART treatment. Interactions between pre-pregnancy BMI and singleton or twin pregnancy with respect to early miscarriage and miscarriage were observed, and twin pregnancy increased the influence of increased pre-pregnancy BMI on early miscarriage and miscarriage. Women before ART treatment should maintain a normal BMI to prevent adverse pregnancy outcomes.

Data Availability Statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics Statement

The studies involving human participants were reviewed and approved by the human research ethics committee of the Northwest Women’s and Children’s Hospital. The ethics committee waived the requirement of written informed consent for participation.

Author Contributions

PQ, SD, WS, JS, and CZ conceived and designed the study. PQ, MY, DZ, DW, and CZ drafted and revised the manuscript. PQ, MY, and DZ analyzed and interpreted the data. PQ, MY, and DZ collected and cleared the data. All authors contributed to the article and approved the submitted version.

Funding

This work was financially supported by “the Fundamental Research Funds for the Central Universities” (China) (no. xzy012019116), the Key Research and Development Program of Shaanxi Province (no. 2020SF-031), and the National Natural Science Foundation of China (no. 81771657).

Conflict of Interest

The 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. The reviewer XL declared a shared affiliation with several of the authors, MY and SD, to the handling editor at time of review.
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