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Carnitine Uptake Defect

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Guidance for primary care clinicians receiving a positive newborn screen result

Other Names

Carnitine transporter deficiency
CUD
Primary carnitine deficiency
Systemic carnitine deficiency (SCD)

ICD-10 Coding

E71.41, Primary carnitine deficiency

Disorder Category

Fatty acid oxidation disorder

Screening

Abnormal Finding

Decreased C0 (free carnitine)

Tested By

Tandem mass spectrometry (MS/MS); sensitivity=100% (80% with the first screen only; specificity=99.97% [Schulze: 2003]

Description

Carnitine uptake defect is caused by a defect in the carnitine transporter in the cell membrane resulting in urinary carnitine wasting, leading to severe systemic and intracellular carnitine deficiency. The latter results in an intramitochondrial defect in the beta-oxidation of fatty acids that impairs energy production and causes the accumulation of free fatty acids. The increased reliance on fat metabolism for energy production during prolonged fasting and/or periods of increased energy demands (fever, stress) may cause metabolic crises in patients with carnitine deficiency. Carnitine uptake defect is caused by having 2 compromising SLC22A5 gene mutations inherited from carrier parents. This gene encodes the protein organic cation transporter 2 (OCTN2), which is responsible for transporting carnitine into cells.

Clinical Characteristics

With treatment for carnitine uptake defect prior to metabolic crises, outcomes are typically excellent with no clinically significant symptoms or medical concerns. Additionally, later treatment may reverse pre-existing cardiomyopathy and muscle weakness, but not developmental delay. Treatment consists of life-long high-dose oral L-carnitine supplementation, with relatively few side effects. [Schimmenti: 2007]
Without treatment, symptoms may vary widely in regard to age of onset, organ involvement, and severity of symptoms depending on the subtype. This would include the metabolic type presenting with metabolic crises and liver disease, myopathic form presenting with cardiomyopathy and skeletal muscle disease, late-onset adulthood type presenting with generalized fatigability, and some who may remain asymptomatic well into adulthood. Patients are at risk of sudden death from arrhythmia at any age.
Initial signs and symptoms of carnitine uptake defect may include:
  • Poor appetite
  • Vomiting
  • Irritability
  • Lethargy
  • Hypoketotic hypoglycemia
  • Sudden death
  • Lab findings:
    • Anemia
    • Metabolic acidosis
    • Hypoglycemia
Subsequent findings include:
  • Muscle weakness
  • Cardiomyopathy
  • Cardiac arrhythmia
  • Hepatomegaly
  • Seizures
  • Brain injury from hypoglycemia

Incidence

The incidence of carnitine uptake deficiency is approximately 1:20,000-70,000 in the US, with about 1% of the normal US population being heterozygous (carriers) for this condition. [Magoulas: 2012] [Amat: 2008]

Inheritance

Autosomal recessive

Primary Care Management

Next Steps After a Positive Screen

Confirming the Diagnosis

  • To confirm the diagnosis of carnitine uptake defect, work with Newborn Screening Services (see RI providers [2]).
  • Follow-up testing will include total and free carnitine analysis in plasma and urine. Rapid screening for severity may include glucose, electrolytes, blood gas, ammonia, liver function tests (LFTs), and creatine phosphokinase (CPK). Molecular genetic testing is confirmatory.
    Plasma carnitines may be measured in the mothers of newborns who screen positive to determine if the screen was a false positive due to severe maternal carnitine deficiency (which may be the result of the mother having a primary carnitine uptake disorder or a maternal diet insufficient in natural carnitine). Carnitine may also be deficient secondary to prematurity, other fatty acid oxidation disorders, or organic acidurias.

If the Diagnosis is Confirmed

Resources

Information & Support

Related Portal Content
After a Diagnosis or Problem is Identified
Families can face a big change when their baby tests positive for a newborn condition. Find information about A New Diagnosis - You Are Not Alone; Caring for Children with Special Health Care Needs; Assistance in Choosing Providers; Partnering with Healthcare Providers, and Top Ten Things to Do After a Diagnosis.

For Professionals

Carnitine Transporter Deficiency - Information for Professionals (STAR-G)Primary Carnitine Deficiency (GARD)Carnitine Deficiency (OMIM)Utah Newborn Screening Program (UDHHS)

For Parents and Patients

Carnitine Transporter Deficiency - Information for Parents (STAR-G)Primary Carnitine Deficiency (MedlinePlus)Fatty Oxidation Disorders (FOD) Family Support Group

Tools

RI ACT Sheet for Carnitine Uptake Defect (ACMG) (PDF Document 141 KB)
Provides recommendations for clinical and laboratory follow-up of the newborn with out-of-range screening results, along with national and local resources for clinicians and families; American College of Medical Genetics.

Confirmatory Algorithms for CO (Free Carnitine) Low / Carnitine Uptake Defect (ACMG)
An algorithm of the basic steps involved in determining the final diagnosis of an infant with a positive newborn screen; American College of Medical Genetics.

Services for Patients & Families in Rhode Island (RI)

For services not listed above, browse our Services categories or search our database.

* number of provider listings may vary by how states categorize services, whether providers are listed by organization or individual, how services are organized in the state, and other factors; Nationwide (NW) providers are generally limited to web-based services, provider locator services, and organizations that serve children from across the nation.

Helpful Articles

PubMed search for articles about carnitine uptake deficiency and neonatal screening

Authors & Reviewers

Initial publication: March 2007; last update/revision: July 2022
Current Authors and Reviewers:
Author: Brian J. Shayota, MD, MPH
Reviewer: Nancy C. Rose, MD
Authoring history
2022: update: Brian J. Shayota, MD, MPHA
2012: revision: Kimberly Hart, MS, LCGCR
2011: first version: Nicola Longo, MD, Ph.D.A
AAuthor; CAContributing Author; SASenior Author; RReviewer

Page Bibliography

Amat di San Filippo C, Taylor MR, Mestroni L, Botto LD, Longo N.
Cardiomyopathy and carnitine deficiency.
Mol Genet Metab.. 2008;94(2):162-166.
Carnitine is essential for the transfer of long-chain fatty acids across the mitochondrial membrane for subsequent beta-oxidation. Study results indicate heterozygosity for primary carnitine deficiency is not more frequent in patients with unselected types of cardiomyopathy and is unlikely to be an important cause of cardiomyopathy in humans.

Magoulas PL, El-Hattab AW, Roy A, Bali DS, Finegold MJ, Craigen WJ.
Diffuse reticuloendothelial system involvement in type IV glycogen storage disease with a novel GBE1 mutation: a case report and review.
Hum Pathol. 2012. PubMed abstract

Schimmenti LA, Crombez EA, Schwahn BC, Heese BA, Wood TC, Schroer RJ, Bentler K, Cederbaum S, Sarafoglou K, McCann M, Rinaldo P, Matern D, di San Filippo CA, Pasquali M, Berry SA, Longo N.
Expanded newborn screening identifies maternal primary carnitine deficiency.
Mol Genet Metab. 2007;90(4):441-5. PubMed abstract
Primary carnitine deficiency impairs fatty acid oxidation and can result in hypoglycemia, hepatic encephalopathy, cardiomyopathy and sudden death. Given the lifetime risk of morbidity or sudden death, identification of adult patients with primary carnitine deficiency is an added benefit of expanded newborn screening programs.

Schulze A, Lindner M, Kohlmuller D, Olgemoller K, Mayatepek E, Hoffmann GF.
Expanded newborn screening for inborn errors of metabolism by electrospray ionization-tandem mass spectrometry: results, outcome, and implications.
Pediatrics. 2003;111(6 Pt 1):1399-406. PubMed abstract