Evidence map›Paper›PMID 42766381›Full record

ArticleEndocrinology, diabetes & metabolism case reports2026

Monoclonal insulin autoimmune syndrome in pregnancy and postpartum.

Anne Cathrine Parelius Wammer, Hanna Dis Margeirsdottir, Geir Erland Tjønnfjord, Ivar Følling

Abstract read
In one paragraph

Article in Endocrinology, diabetes & metabolism case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Anne Cathrine Parelius WammerAkershus University Hospital, Department of Endocrinology , Lørenskog, Norway.ORCID 0000-0001-7482-860X
Hanna Dis MargeirsdottirOslo University Hospital, Division of Pediatric and Adolescent Medicine , Oslo, Norway.
Geir Erland TjønnfjordOslo University Hospital, Department of Haematology , Oslo, Norway.
Ivar FøllingAkershus University Hospital, Department of Endocrinology , Lørenskog, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

summaryIn insulin autoimmune syndrome (IAS), high levels of anti-insulin antibodies cause hypoglycemic episodes. Pregnancy in patients with IAS raises several concerns. The mother may experience glucose imbalances affecting the mother and fetus, transfer of antibodies may induce glucose disturbances in the fetus, and the antibodies may cause IAS in the newborn child. We present the first case of pregnancy and the postpartum period in monoclonal IAS, discuss pathogenetic mechanisms, and recommend how to handle future cases. A patient with monoclonal IAS was treated successfully with daratumumab to decrease anti-insulin antibodies from 1,840 U/mL (<0.4) to 180 U/mL. Treatment was paused to facilitate pregnancy, and after four months she conceived. Her antibody levels remained stable, and she was euglycemic during her pregnancy. The fetus grew at a normal rate. At delivery, the anti-insulin antibody level in the mother was 74 U/mL. The newborn had a level of 38 U/mL, which disappeared within 21 weeks. The child experienced no abnormal glucose fluctuations. The mother's IAS relapsed a few days postpartum, with hypoglycemia and anti-insulin antibody levels rising to 946 U/mL. Treatment with daratumumab was resumed efficaciously. The pregnancy went well for the mother, fetus, and child, probably mainly because of the relatively low levels of anti-insulin antibodies. We discuss possible explanations for the recurrence of IAS in the mother postpartum. LEARNING POINTS:

Indexed as

autoimmunityHirata’s diseasehypoglycemiainsulin autoimmune syndromemonoclonalitypregnancy

Identifiers

PMID42766381
PMCPMC13617637

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.