Objective To compare the metabolic status of preschool singleton children conceived by assisted reproductive technology (ART) with naturally conceived (NC) singleton children, so as to provide evidence for the health management of ART-conceived children. Methods A total of 70 ART-conceived singleton children aged 36 - 72 months who underwent physical examination at the Dalian Women and Children's Medical Group from January 2023 to January 2025 were enrolled, and 70 age-matched NC singleton children were included at a 1∶1 ratio during the same period. Parental demographics, perinatal information, and the children's feeding and dietary habits were collected. Anthropometric measurements (height, weight, waist circumference) and blood pressure were assessed. Fasting blood glucose (FBG), fasting insulin (FINS), triglycerides (TG), total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), apolipoprotein A1 (ApoA1), and apolipoprotein B (ApoB) levels were measured. Multiple linear regression models were employed to adjust for potential confounding factors, including dietary habits and parental body mass index (BMI). Results Parents in the ART group had significantly older reproductive ages and lower gestational weight gain than those in the NC group (t=6.761, 6.032,-2.329, P<0.05). After adjustment for confounding factors, there were no statistically significant differences in body weight, height, body mass index, or blood pressure between the two groups (P>0.05). However, waist circumference was significantly greater in the ART group than in the NC group (β=2.022, P<0.05). After adjustment, TG and ApoB levels remained significantly higher in the ART group(β=0.104,0.038), while HDL-C and ApoA1 levels were significantly lower than those in the NC group (β=-0.298,-0.105,P<0.05). No significant differences were found in TC, LDL-C, FBG, FINS, or HOMA-IR between the two groups (P>0.05). There were no significant differences in the detection rates of abnormal blood pressure, dyslipidemia, or impaired blood glucose between the two groups (P>0.05). The detection rate of overweight/obesity was significantly higher in the ART group than in the NC group (Z=-2.233, P<0.05). Conclusions Preschool singleton children conceived by ART exhibit differences in several blood lipid parameters, including TG, HDL-C, ApoB, and ApoA1. However, these differences do not increase the risk of dyslipidemia. Increased waist circumference and a higher prevalence of overweight/obesity are observed in ART-conceived children, highlighting the importance of long-term monitoring of nutritional and metabolic status in this population to prevent obesity and related metabolic disorders.
Key words
assisted reproductive technology /
singleton children /
preschool age /
metabolic status
{{custom_sec.title}}
{{custom_sec.title}}
{{custom_sec.content}}
References
[1] 黄荷凤. 实用人类辅助生殖技术[M]. 北京: 人民卫生出版社, 2018.
[2] Cui L, Zhou W, Xi B, et al. Increased risk of metabolic dysfunction in children conceived by assisted reproductive technology[J]. Diabetologia, 2020, 63(10): 2150-2157.
[3] Le F, Lou HY, Wang QJ, et al. Increased hepatic INSIG-SCAP-SREBP expression is associated with cholesterol metabolism disorder in assisted reproductivetechnology-conceived aged mice[J]. Reprod Toxicol, 2019, 84: 9-17.
[4] Wang J, Chen L, Yong Y, et al. Comprehensivehealth assessment of school-age children conceived by assisted reproductive technology: A prospective cohort follow-up study[J]. BJOG, 2025, 132(Suppl 2): 8-17.
[5] Marleen S, Kodithuwakku W, Nandasena R, et al. Maternal and perinatal outcomes in twin pregnancies following assisted reproduction:A systematic review and meta-analysis involving 802 462 pregnancies[J]. Hum Reprod Update, 2024, 30(3): 309-322.
[6] Garner J, Parisaei M, Shah A. Re: Obstetric and neonatal complications in pregnancies conceived after oocyte donation:A systematic review and meta-analysis: Significance of advising women prior to fertility treatment[J]. BJOG, 2017, 124(9): 1451-1452.
[7] Li W, Zhao J, Ni M, et al. Assisted reproductive technology and neurodevelopmental outcomes in offspring:A prospective birth cohort study in East China[J]. Reprod Biomed Online, 2023, 46(6): 983-994.
[8] Tocariu R, Dinulescu A, Prejmereanu A, et al. Riskfactors for prematurity and congenital malformations in assisted reproductive technology pregnancies—a retrospective study[J]. J Clin Med, 2024, 13(21): 6470.
[9] Ajeen R, Turk-Adawi KI, Ammerman AS, et al. Assessing the relationship between anthropometric indices and visceral adipose tissue: A cross-sectional study in a Qatari population[J]. J Int Med Res, 2025, 53(9): 3000605251371603.
[10] Ross R, Neeland IJ, Yamashita S, et al. Waist circumference as a vital sign in clinical practice:A Consensus Statement from the IAS and ICCR Working Group on Visceral Obesity[J]. Nat Rev Endocrinol, 2020, 16(3): 177-189.
[11] Ono M, Kuji N, Ueno K, et al. The long-term outcome of children conceived through assisted reproductive technology[J]. Reprod Sci, 2024, 31(3): 583-590.
[12] Langer M, Vilsmaier T, Kramer M, et al. Vascular health in adults born after using assisted reproductive technologies[J]. Pediatr Cardiol, 2024, 45(6): 1242-1250.
[13] Zhang S, Luo Q, Meng R, et al. Long-term health risk of offspring born from assisted reproductive technologies[J].J Assist Reprod Genet, 2024, 41(3): 527-550.
[14] Ilmuratova S, Manzhuova L, Bazarbayeva A, et al. Focus on the endocrine system of children born after reproductive technologies in Kazakhstan[J]. Qatar Med J, 2025, 2025(1): 9.
[15] Narapareddy L, Rhon-Calderon EA, Vrooman LA, et al. Sex-specific effects of in vitro fertilization on adult metabolic outcomes and hepatic transcriptome and proteome in mouse[J].FASEB J, 2021, 35(4): e21523.
[16] Wu W, Ji M, Yang J, et al. ART altered DNA methylation of the imprinted gene H19 in fetal tissue after multifetal pregnancy reduction[J].J Assist Reprod Genet, 2024, 41(11): 3039-3049.
[17] Graham ME, Jelin A, Hoon AH Jr, et al. Assisted reproductive technology: Short- and long-term outcomes[J].Dev Med Child Neurol, 2023, 65(1): 38-49.
[18] Wahl S, Drong A, Lehne B, et al. Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity[J]. Nature, 2017, 541(7635): 81-86.
[19] Mendelson MM, Marioni RE, Joehanes R, et al. Association ofbody mass index with DNA methylation and gene expression in blood cells and relations to cardiometabolic disease: A Mendelian randomization approach[J]. PLoS Med, 2017, 14(1): e1002215.
[20] Asserhøj LL, Mizrak I, Lebech Kjaer AS, et al. Blood pressure and lipid profiles in children born after ART with frozen embryo transfer[J].Hum Reprod Open, 2024, 2024(2): hoae016.
[21] Cui Y, Wang Y, Wang X, et al. Metabolicstatus and expression level of SREBP mRNA and mir-33 among children conceived by assisted reproductive technology[J]. Int J Genomics, 2025, 2025: 2271298.
[22] Catford SR, McLachlan RI, O'Bryan MK, et al. Long-term follow-up of ICSI-conceived offspring compared with spontaneously conceived offspring: A systematic review of health outcomes beyond the neonatal period[J]. Andrology, 2018, 6(5): 635-653.
[23] Wijs LA, Doherty DA, Keelan JA, et al. Comparison of the cardiometabolic profiles of adolescents conceived through ART with those of a non-ART cohort[J]. Hum Reprod,2022, 37(8): 1880-1895.