The association of falling insulin requirements with maternal biomarkers and placental dysfunction: A prospective study of women with preexisting diabetes in pregnancy

dc.contributor.authorPadmanabhan, Suja
dc.contributor.authorLee, Vincent W. S
dc.contributor.authorMclean, Marc
dc.contributor.authorAthayde, Neil
dc.contributor.authorLanzarone, V
dc.contributor.authorKhoshnow, Qemer
dc.contributor.authorPeek, Michael
dc.contributor.authorCheung, N Wah
dc.date.accessioned2021-09-23T04:57:55Z
dc.date.issued2017
dc.date.updated2020-11-23T11:14:33Z
dc.description.abstractOBJECTIVE To investigate the association of falling insulin requirements (FIR) among women with preexisting diabetes with adverse obstetric outcomes and maternal biomarkers longitudinally in pregnancy. RESEARCH DESIGN AND METHODS A multicenter prospective cohort study of 158 women (41 with type 1 diabetes and 117 with type 2 diabetes) was conducted. Women with FIR of ≥15% from the peak total daily dose after 20 weeks' gestation were considered case subjects (n = 32). The primary outcome was a composite of clinical markers of placental dysfunction (preeclampsia, small for gestational age [≤5th centile], stillbirth, premature delivery [<30 weeks], and placental abruption). Maternal circulating angiogenic markers (placental growth factor [PlGF] and soluble fms-like tyrosine kinase 1 [sFlt-1]), placental hormones (human placental lactogen, progesterone, and tumor necrosis factor-α), HbA1c, and creatinine were studied serially during pregnancy. RESULTS FIR ≥15% were associated with an increased risk of the composite primary outcome (odds ratio [OR] 4.38 [95% CI 1.9–10.3]; P < 0.001), preeclampsia (OR 6.76 [95% CI 2.7–16.7]; P < 0.001), and was more common among women with type 1 diabetes (36.6 vs. 14.5%; P = 0.002). Creatinine was modestly elevated among women with FIR ≥15%; however, there was no difference in HbA1c. The ratio of sFlt-1 to PlGF was significantly higher among women with FIR at 25, 30, and 36 weeks, with differences maintained in the subgroup that developed preeclampsia. There was no difference in placental hormones between the groups. CONCLUSIONS This is the first prospective study to associate FIR with altered expression of placental antiangiogenic factors and preeclampsia. FIR are an important clinical sign, among women with preexisting diabetes, that should alert the clinician to investigate underlying placental dysfunction.en_AU
dc.description.sponsorshipThe authors thank Westmead Medical Research Foundation for funding the study.en_AU
dc.format.mimetypeapplication/pdfen_AU
dc.identifier.issn0149-5992en_AU
dc.identifier.urihttp://hdl.handle.net/1885/248715
dc.language.isoen_AUen_AU
dc.publisherAmerican Diabetes Associationen_AU
dc.rights© 2017 by the American Diabetes Associationen_AU
dc.sourceDiabetes Careen_AU
dc.titleThe association of falling insulin requirements with maternal biomarkers and placental dysfunction: A prospective study of women with preexisting diabetes in pregnancyen_AU
dc.typeJournal articleen_AU
local.bibliographicCitation.issue10en_AU
local.bibliographicCitation.lastpage1330en_AU
local.bibliographicCitation.startpage1323en_AU
local.contributor.affiliationPadmanabhan, Suja, Westmead Hospital, Sydneyen_AU
local.contributor.affiliationLee, Vincent W. S, University of Sydneyen_AU
local.contributor.affiliationMclean, Marc, Westmead Hospital, Sydneyen_AU
local.contributor.affiliationAthayde, Neil, Westmead Hospital, Sydneyen_AU
local.contributor.affiliationLanzarone, V, Nepean Hospitalen_AU
local.contributor.affiliationKhoshnow, Qemer, Nepean Hospital, Sydneyen_AU
local.contributor.affiliationPeek, Michael, College of Health and Medicine, ANUen_AU
local.contributor.affiliationCheung, N Wah, University of Sydneyen_AU
local.contributor.authoruidPeek, Michael, u1005089en_AU
local.description.embargo2099-12-31
local.description.notesImported from ARIESen_AU
local.identifier.absfor111402 - Obstetrics and Gynaecologyen_AU
local.identifier.absseo920114 - Reproductive System and Disordersen_AU
local.identifier.absseo920104 - Diabetesen_AU
local.identifier.ariespublicationa383154xPUB8877en_AU
local.identifier.citationvolume40en_AU
local.identifier.doi10.2337/dc17-0391en_AU
local.identifier.scopusID2-s2.0-85032615029
local.publisher.urlhttp://www.diabetes.org/en_AU
local.type.statusPublished Versionen_AU

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