Absence of the G1528C (E474Q) mutation in the α-subunit of the mitochondrial trifunctional protein in women with acute fatty liver of pregnancy

Anirban Maitra, Rana Domiati-Saad, Nicole Yost, Gary Cunningham, Beverly Barton Rogers, Michael J. Bennett

Research output: Contribution to journalArticle

Abstract

Acute fatty liver of pregnancy (AFLP) is a rare and dreaded complication of pregnancy, almost exclusively seen in the third trimester. The histopathologic features of AFLP closely resemble those seen in metabolic disorders characterized by deficiency of fatty acid oxidative enzymes. Several reports have established a strong association between AFLP in the mother and fetal deficiency of the enzyme long-chain L-3-hydroxyacyl-CoA dehydrogenase (LCHAD). However, these studies have an inevitable selection bias resulting from ascertainment through an affected infant, rather than an unselected population of patients with AFLP. We retrospectively examined a series of 10 women with pregnancies complicated by AFLP to determine the prevalence of the common LCHAD mutation (G1528C) in this population. The existing LCHAD primers, which produce a 640-bp amplicon (IJlst L, Ruiter JP, Hoovers JM, Jakobs ME, Wanders RJ: J Clin Invest 98:1028-1033, 1996), were modified to make them amenable to analysis of fragmented DNA obtained from microdissected formalin-fixed material. None of the patients were found to harbor the common G1528C mutation. It is likely that AFLP arising in the context of fetal LCHAD deficiency represents only one of the possible etiologies for this uncommon disorder, and the metabolic basis of AFLP is more heterogeneous than previously believed.

Original languageEnglish (US)
Pages (from-to)658-661
Number of pages4
JournalPediatric Research
Volume51
Issue number5
Publication statusPublished - 2002
Externally publishedYes

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Maitra, A., Domiati-Saad, R., Yost, N., Cunningham, G., Barton Rogers, B., & Bennett, M. J. (2002). Absence of the G1528C (E474Q) mutation in the α-subunit of the mitochondrial trifunctional protein in women with acute fatty liver of pregnancy. Pediatric Research, 51(5), 658-661.