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Observational Study
. 2017 May;96(21):e6540.
doi: 10.1097/MD.0000000000006540.

Thalidomide results in diminished ovarian reserve in reproductive age female IBD patients

Affiliations
Observational Study

Thalidomide results in diminished ovarian reserve in reproductive age female IBD patients

Xiang Peng et al. Medicine (Baltimore). 2017 May.

Abstract

The effectiveness of thalidomide in treating inflammatory bowel disease (IBD) has been widely recognized. Meanwhile, many serious adverse drug reactions have been observed, but no know reports on ovarian reserve function.Female patients, ranging in age between 18 and 40, were referred to our institution to undergo sex hormone detection and ultrasonic scanning for ovarian function assessment, between February 1, 2016 and September 31, 2016.Thirty-three patients treated with thalidomide (group A), 73 patients without thalidomide (group B), and 78 healthy women as control were studied. Menstrual disorder was higher in group A than group B (78.8% vs 57.2%, P < 0.05), and both groups were higher than control group 33.3%, P < 0.05. Anti-Mullerian hormone (AMH) levels and antral follicle count (AFC) in group A were lower than group B, P < 0.05, while estradiol (E2) and follicle-stimulating hormone (FSH) levels were no different between 2 groups. Crohn Disease Endoscopic Index of Severity (CDEIS) and thalidomide were the independent risk factors in diminished ovarian reserve (DOR), and when dose reached 75 mg/day, 5 g total, or when treatment time reached 10 months respectively. These influence may increasing (P < 0.05), but they may recover after stopping (P < 0.05).Thalidomide was an independent risk factor leading to DOR in female IBD patients, the influence may increasing when daily dose and accumulated dose reached 75 mg/day and 5 g total dose, but may be reversed by stopping.

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Conflict of interest statement

The authors have no conflicts of interest to disclose.

Figures

Figure 1
Figure 1
AMH changes before and after using thalidomide or AZA = azathioprine.
Figure 2
Figure 2
The relationship between thalidomide dose, accumulative dose, prescription time with AMH.

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References

    1. McBride WG. Thalidomide and congenital abnormalities. Lancet 1961;7216:1358.
    1. Sheskin J. Thalidomide in the treatment of lepra reactions. Clin Pharmacol Ther 1965;6:303–6. - PubMed
    1. Highleyman L. FDA approves fomivirsen, famciclovir, and Thalidomide. Food and Drug Administration. BETA 1998;10:5. - PubMed
    1. Franks ME, Macpherson GR, Figg WD. Thalidomide. Lancet 2004;9423:1802–11. - PubMed
    1. Plamondon S, Ng SC, Kamm MA. Thalidomide in luminal and fistulizing Crohn's disease resistant to standard therapies. Aliment Pharmacol Ther 2007;5:557–67. - PubMed

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