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. 2023 Feb 7;16(1):34.
doi: 10.1186/s13048-023-01112-6.

Clinical characteristics and risk factors of ovarian reserve decreases in women with Crohn's disease: a case-control study

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Clinical characteristics and risk factors of ovarian reserve decreases in women with Crohn's disease: a case-control study

Peng Xiang et al. J Ovarian Res. .

Abstract

Background: Crohn's disease (CD), often occurring in women of child-bearing age, can decline the fertility rate. However, whether it reduces ovarian reserve has been rarely reported. This study aimed to evaluate the ovarian reserve in women with CD from the perspective of anti-Müllerian hormone (AMH), and explore the factors that can decrease ovarian reserve.

Methods: A case-control retrospective study was designed. We analyzed the AMH levels in a total of 135 CD women and 878 healthy controls. Through propensity score matching, the subjects were assigned in a ratio of 1:3 to CD group (n = 121) and control group (n = 324). Both groups shared similar basic characteristics, like age, body mass index and smoking status. Serum AMH levels were measured by chemiluminescence.

Results: The AMH level in the CD group was significantly lower than that in the control group (2.17 ± 2.23 μg/L vs 3.95 ± 2.01 μg/L, 95%CI [1.34-2.21], P < 0.001). In both groups, the AMH levels decreased as age increased, but without between-group difference in the decreasing rate (P = 0.639). Multivariate analysis showed that age > 30 years (OR, 2.905; 95%CI [1.053-8.531], P = 0.017), disease activity (OR,4.314; 95%CI [1.561-12.910], P = 0.002) and thalidomide use (OR,12.628; 95%CI [4.351 -42.820], P < 0.001) were independent risk factors associated with decreased ovarian reserve (AMH<1.1μg/L).

Conclusion: Ovarian reserve is lower in CD women than in healthy women. Age, CD activity and medication of thalidomide are risk factors that can aggravate the decline of ovarian reserve.

Keywords: Anti-Müllerian hormone; Crohn’s disease; Ovarian reserve.

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Conflict of interest statement

The authors declare no competing interests.

Figures

Fig. 1
Fig. 1
Comparison of AMH between CD patients and control
Fig. 2
Fig. 2
Relationship between AMH and age in CD and control group
Fig. 3
Fig. 3
Risk factors associated with decreased ovarian reserve

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References

    1. Duricova D, Burisch J, Jess T, Gower-Rousseau C, Lakatos PL, EpiCom E. Age-related differences in presentation and course of inflammatory bowel disease: an update on the population-based literature. J Crohns Colitis. 2014;8(11):1351–1361. doi: 10.1016/j.crohns.2014.05.006. - DOI - PubMed
    1. Mountifield R, Bampton P, Prosser R, Muller K, Andrews JM. Fear and fertility in inflammatory bowel disease: a mismatch of perception and reality affects family planning decisions. Inflamm Bowel Dis. 2009;15(5):720–725. doi: 10.1002/ibd.20839. - DOI - PubMed
    1. Druvefors E, Landerholm K, Hammar U, Myrelid P, Andersson RE. Impaired fertility in women with inflammatory bowel disease: a National Cohort Study from Sweden. J Crohns Colitis. 2021;15(3):383–390. doi: 10.1093/ecco-jcc/jjaa191. - DOI - PMC - PubMed
    1. Clark-Snustad K, Butnariu M, Afzali A. Women's health and ulcerative colitis. Gastroenterol Clin N Am. 2020;49(4):769–789. doi: 10.1016/j.gtc.2020.07.004. - DOI - PubMed
    1. Peng X, Zhi M, Wei M, Li TT, Zhang M, Zhang YQ, et al. Thalidomide results in diminished ovarian reserve in reproductive age female IBD patients. Medicine (Baltimore) 2017;96(21):e6540. doi: 10.1097/MD.0000000000006540. - DOI - PMC - PubMed