Thompson, M and Hogg, P and De Paoli, A and Burgess, J, Parental multiple endocrine Neoplasia Type 1 (MEN 1) is associated with increased offspring childhood mortality, Journal of Clinical Endocrinology and Metabolism, 105, (4) pp. e1106-e1114. ISSN 0021-972X (2020) [Refereed Article]
Copyright 2019 Endocrine Society
Context: Information regarding the impact of parental multiple endocrine neoplasia type 1 (MEN 1) on neonatal outcomes is limited to case reports.
Objective: To determine the impact of parental MEN 1 on neonatal outcomes.
Methods: Retrospective cohort analysis of the Tasman 1 MEN 1 kindred stratified by whether birth occurred before ("historical cohort") or after ("contemporary cohort") prospective screening commenced. The historical cohort included kindred members born between 1825 and 1984 (n = 341 children with a MEN 1 positive (MEN 1+ ) parent and n = 314 children with MEN 1 negative (MEN 1– ) parents). The contemporary cohort included neonates (n = 52) of MEN 1+ women (n = 21) managed at a tertiary referral hospital between 1985 and 2018.
Results: Historical cohort: compared with MEN 1– parents, children of MEN 1+ parents were more likely to die postpartum (HR 4.6, P = .046 at 6 months of age). Excess mortality at 15 years of age was observed for children of MEN 1+ mothers (HR 8.50, P = .002) and fathers (HR 3.82, P = .03). Contemporary cohort: neonates of MEN 1+ mothers were more likely to have low birth weight (28.9% vs 6.7%, P = .01), be admitted to a higher care nursery (40.4% vs 17%, P = .02), and require a longer median postnatal stay (5 vs 4 days, P = .009) than the Australian average. Isolated antenatal hypercalcemia did not significantly alter neonatal outcomes.
Conclusion: Children with a MEN 1+ parent are disproportionately vulnerable postpartum. Neonates of MEN 1+ mothers remain vulnerable despite contemporary care. The excess risk was not fully explained by maternal MEN 1 or antenatal hypercalcemia.
|Item Type:||Refereed Article|
|Keywords:||parental, MEN 1, childhood, mortality|
|Research Division:||Biomedical and Clinical Sciences|
|Research Group:||Clinical sciences|
|Objective Group:||Clinical health|
|Objective Field:||Clinical health not elsewhere classified|
|UTAS Author:||De Paoli, A (Dr Tony De Paoli)|
|UTAS Author:||Burgess, J (Professor John Burgess)|
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