The Invitae Cerebral Creatine Deficiency Panel analyzes the three genes that are associated with defects in the biosynthesis or transport of creatine. This test is useful for the diagnosis of patients in whom L-arginine:glycine amidinotransferase (AGAT) deficiency, guanidinoacetate methyltransferase (GAMT) deficiency, or creatine transporter deficiency is suspected due to clinical symptoms or abnormal laboratory findings. Genetic testing of these genes may confirm a diagnosis and help guide treatment and management decisions.
GAMT GATM SLC6A8
GAMT GATM SLC6A8
The cerebral creatine deficiency syndromes are a group of three inherited disorders that affect the biosynthesis or transport of creatine, which leads to a deficiency of creatine in the brain that can be detected by MR spectroscopy (1H-MRS). Most patients develop intellectual disability and seizures.
Patients with L:arginine:glycine amidinotransferase (AGAT) deficiency have been diagnosed from 3 weeks to 25 years; however, symptoms may be present much earlier. Most patients with this disorder have varying degrees of intellectual disability and speech delay. More than half of patients have been reported with muscle myopathy, and approximately one-third have autistic features and behavioral disturbances. Seizures are a rare finding in this disorder. Patients with AGAT deficiency will have low urine and plasma guanidinoacetate, with low to low-normal plasma creatine. The urine creatine/creatinine ratio will be low normal. Creatine supplementation is used to treat individuals with AGAT deficiency. Onset of treatment and whether the patient is already symptomatic at the time of treatment can impact the effectiveness of creatine supplementation.
Patients with guanidinoacetate methyltransferase (GAMT) deficiency typically present from three months to three years of age. All patients have intellectual disability and seizures; these symptoms can range from mild to severe, with most patients having severe disease (~60%). Most patients will also have a movement disorder and behavior disorder. Symptoms can include dystonia, chorea, athetosis, ataxia, hyperactivity, autism, and self-injurious behavior. Patients with GAMT deficiency will have elevated guanidinoacetate in urine and plasma, with low plasma creatine, low to low-normal urine creatine, and a low to low-normal urine creatine/creatinine ratio. Creatine supplementation with ornithine supplementation and arginine restriction have been used to treat GAMT deficiency. Sodium benzoate may also be given to reduce glycine levels (elevated levels are a precursor of guanidinoacetate). Improvement of clinical symptoms have been reported in patients, but the degree of improvement may depend on the onset of therapy.
Patients with X-linked creatine transporter deficiency typically present within the first three years of life. Phenotypic features can range from mild to severe. All males have been reported with intellectual disability and speech delay. Behavior disorder is present in most males and can include attention deficit, autistic features, social anxiety, aggressiveness, stereotypic behaviors, impulsive behavior, and self-injurious behavior. Seizures have been reported in more than half of males with creatine transporter deficiency. Other symptoms observed include hypotonia, movement disorder, dysmorphic features, gastrointestinal disease, and (rarely) cardiac findings. Heterozygous females have been reported with features that range from asymptomatic to mild intellectual disability. Both males and females with creatine transporter deficiency will have normal plasma guanidinoacetate and creatine. Urine guanidinoacetate will be normal, with normal to elevated urine creatine. Males will have elevated creatine/creatinine ratios in urine while females may be normal to mildly elevated. Creatine supplementation along with arginine and glycine supplementation has been used to treat creatine transporter deficiency in both males and females, with mixed results. Earlier initiation of treatment may improve long-term outcome, but this has not been proven.
The clinical sensitivity of this test is dependent on the patient’s underlying genetic condition. This test covers all of the primary genetic causes of cerebral creatine deficiency. For each condition, the chart below shows the percentage of attributable clinical cases and the percentage of clinical cases in which either biallelic pathogenic variants (for AGAT and GAMT deficiencies) or a single pathogenic variant (for creatine transporter deficiency) is expected to be identified through analysis of the genes on this panel.
|Gene||Disorder||% of cerebral creatine deficiency cases attributed||Clinical sensitivity by underlying condition|
|SLC6A8||Creatine transporter deficiency||56%||~100%|
AGAT and GAMT deficiencies are inherited in an autosomal recessive manner. Creatine transporter deficiency is inherited in an X-linked manner.
The prevalence of cerebral creatine deficiency is dependent on the underlying condition. The prevalence of GAMT deficiency has been estimated at 1 in 550,000–2,640,000. The overall prevalence of creatine transporter deficiency is not known, but it has an estimated prevalence of 1%–2% in families with X-linked intellectual disability. AGAT deficiency is a rare disorder with an unknown prevalence.
Invitae is a College of American Pathologists (CAP)-accredited and Clinical Laboratory Improvement Amendments (CLIA)-certified clinical diagnostic laboratory performing full-gene sequencing and deletion/duplication analysis using next-generation sequencing technology (NGS).
Our sequence analysis covers clinically important regions of each gene, including coding exons, +/- 10 base pairs of adjacent intronic sequence, and select noncoding variants. Our assay provides a Q30 quality-adjusted mean coverage depth of 350x (50x minimum, or supplemented with additional analysis). Variants classified as pathogenic or likely pathogenic are confirmed with orthogonal methods, except individual variants that have high quality scores and previously validated in at least ten unrelated samples.
Our analysis detects most intragenic deletions and duplications at single exon resolution. However, in rare situations, single-exon copy number events may not be analyzed due to inherent sequence properties or isolated reduction in data quality. If you are requesting the detection of a specific single-exon copy number variation, please contact Client Services before placing your order.
|Gene||Transcript reference||Sequencing analysis||Deletion/Duplication analysis|