Literature DB >> 33818043

False-positive very long-chain fatty acids in a case of autoimmune adrenal insufficiency.

Jia Zhu1, David T Breault1.   

Abstract

BACKGROUND: X-linked adrenoleukodystrophy (ALD) affects up to 25% of boys diagnosed with adrenal insufficiency in childhood. Because early identification of these individuals can be lifesaving, all boys with new-onset primary adrenal insufficiency should be tested for ALD with a plasma very long-chain fatty acid (VLCFA) level. While plasma VLCFA is a diagnostic test with high sensitivity and specificity, false-positive results have been reported in individuals on a ketogenic diet. CASE
PRESENTATION: We present a case of an 11-year-old boy with new-onset primary adrenal insufficiency due to autoimmune adrenalitis who was initially found to have elevated VLCFA levels, suggestive of ALD, that normalized on repeat testing.
CONCLUSIONS: As advances in gene therapy and newborn screening for ALD expand, VLCFA testing may increase, and clinicians should be aware that testing during the initial presentation of primary adrenal insufficiency may lead to false-positive results and associated psychosocial distress.
© 2020 Walter de Gruyter GmbH, Berlin/Boston.

Entities:  

Keywords:  Addison’s disease; VLCFA; adrenoleukodystrophy

Mesh:

Substances:

Year:  2020        PMID: 33818043      PMCID: PMC9093155          DOI: 10.1515/jpem-2020-0652

Source DB:  PubMed          Journal:  J Pediatr Endocrinol Metab        ISSN: 0334-018X            Impact factor:   1.520


  14 in total

1.  Newborn screening for X-linked adrenoleukodystrophy in New York State: diagnostic protocol, surveillance protocol and treatment guidelines.

Authors:  B H Vogel; S E Bradley; D J Adams; K D'Aco; R W Erbe; C Fong; A Iglesias; D Kronn; P Levy; M Morrissey; J Orsini; P Parton; J Pellegrino; C A Saavedra-Matiz; N Shur; M Wasserstein; G V Raymond; M Caggana
Journal:  Mol Genet Metab       Date:  2015-02-12       Impact factor: 4.797

2.  Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls.

Authors:  A B Moser; N Kreiter; L Bezman; S Lu; G V Raymond; S Naidu; H W Moser
Journal:  Ann Neurol       Date:  1999-01       Impact factor: 10.422

Review 3.  The Changing Face of Adrenoleukodystrophy.

Authors:  Jia Zhu; Florian Eichler; Alessandra Biffi; Christine N Duncan; David A Williams; Joseph A Majzoub
Journal:  Endocr Rev       Date:  2020-08-01       Impact factor: 19.871

4.  Increased very long chain fatty acids in patients on a ketogenic diet: a cause of diagnostic confusion.

Authors:  C Theda; R C Woody; S Naidu; A B Moser; H W Moser
Journal:  J Pediatr       Date:  1993-05       Impact factor: 4.406

5.  Investigational methods for peroxisomal disorders.

Authors:  Steven Steinberg; Richard Jones; Carol Tiffany; Ann Moser
Journal:  Curr Protoc Hum Genet       Date:  2008-07

6.  Hematopoietic Stem-Cell Gene Therapy for Cerebral Adrenoleukodystrophy.

Authors:  Florian Eichler; Christine Duncan; Patricia L Musolino; Paul J Orchard; Satiro De Oliveira; Adrian J Thrasher; Myriam Armant; Colleen Dansereau; Troy C Lund; Weston P Miller; Gerald V Raymond; Raman Sankar; Ami J Shah; Caroline Sevin; H Bobby Gaspar; Paul Gissen; Hernan Amartino; Drago Bratkovic; Nicholas J C Smith; Asif M Paker; Esther Shamir; Tara O'Meara; David Davidson; Patrick Aubourg; David A Williams
Journal:  N Engl J Med       Date:  2017-10-04       Impact factor: 91.245

7.  X-linked adrenoleukodystrophy is a frequent cause of idiopathic Addison's disease in young adult male patients.

Authors:  S Laureti; G Casucci; F Santeusanio; G Angeletti; P Aubourg; P Brunetti
Journal:  J Clin Endocrinol Metab       Date:  1996-02       Impact factor: 5.958

Review 8.  Adrenoleukodystrophy - neuroendocrine pathogenesis and redefinition of natural history.

Authors:  Stephan Kemp; Irene C Huffnagel; Gabor E Linthorst; Ronald J Wanders; Marc Engelen
Journal:  Nat Rev Endocrinol       Date:  2016-06-17       Impact factor: 43.330

9.  A report on state-wide implementation of newborn screening for X-linked Adrenoleukodystrophy.

Authors:  Katie Wiens; Susan A Berry; Hyoung Choi; Amy Gaviglio; Ashish Gupta; Amy Hietala; Daniel Kenney-Jung; Troy Lund; Weston Miller; Elizabeth I Pierpont; Gerald Raymond; Holly Winslow; Heather A Zierhut; Paul J Orchard
Journal:  Am J Med Genet A       Date:  2019-05-10       Impact factor: 2.802

10.  Evaluation of X-Linked Adrenoleukodystrophy Newborn Screening in North Carolina.

Authors:  Stacey Lee; Kristin Clinard; Sarah P Young; Catherine W Rehder; Zheng Fan; Ali S Calikoglu; Deeksha S Bali; Donald B Bailey; Lisa M Gehtland; David S Millington; Hari S Patel; Sara E Beckloff; Scott J Zimmerman; Cynthia M Powell; Jennifer L Taylor
Journal:  JAMA Netw Open       Date:  2020-01-03
View more
  1 in total

Review 1.  ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy.

Authors:  Alyssa M Volmrich; Lauren M Cuénant; Irman Forghani; Sharon L Hsieh; Lauren T Shapiro
Journal:  Appl Clin Genet       Date:  2022-08-12
  1 in total

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