Abstract | AIMS: To evaluate the number and nature of reported congenital malformations (CMs) after intrauterine exposure to non-tumour necrosis factor inhibitor biologics (non-TNFi biologics) compared to certolizumab pegol (CZP). METHODS: RESULTS:
ORs were not statistically significant except for belimumab and vedolizumab (similar in magnitude). Except for vedolizumab, no specific CM patterns were observed for the included non-TNFi biologics. Three cases of corpus callosum agenesis (CCA) were identified for vedolizumab (versus none in CZP and other investigated non-TNFi biologics). Two of the CCA cases were associated with other neurological CMs (one cerebral ventriculomegaly with microcephaly and one polymicrogyria). This may indicate that these CCAs are related to undiagnosed genetic alterations or are associated with the underlying maternal disease, although a definite relationship with vedolizumab exposure cannot be ruled out. CONCLUSION:
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Authors | Nafise Ghalandari, Hubertina J M J Crijns, Jorieke E H Bergman, Radboud J E M Dolhain, Eugène P van Puijenbroek, Johanna M W Hazes |
Journal | British journal of clinical pharmacology
(Br J Clin Pharmacol)
Vol. 88
Issue 12
Pg. 5378-5388
(12 2022)
ISSN: 1365-2125 [Electronic] England |
PMID | 35894810
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2022 The Authors. British Journal of Clinical Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society. |
Chemical References |
- Abatacept
- Antirheumatic Agents
- Biological Products
- Certolizumab Pegol
- Interleukin 1 Receptor Antagonist Protein
- Rituximab
- Tumor Necrosis Factor-alpha
- Ustekinumab
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Topics |
- Humans
- Abatacept
- Antirheumatic Agents
(adverse effects)
- Arthritis, Rheumatoid
(drug therapy)
- Biological Products
(adverse effects)
- Certolizumab Pegol
(adverse effects)
- Interleukin 1 Receptor Antagonist Protein
(therapeutic use)
- Necrosis
- Retrospective Studies
- Rituximab
(therapeutic use)
- Tumor Necrosis Factor-alpha
- Ustekinumab
(therapeutic use)
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