SCP2 gene is located on chromosome 1p32 and encodes two distinct proteins, sterol carrier protein X (SCPx) and sterol carrier protein 2 (SCP2), via separate promoters (1). SCPx functions as a peroxisomal enzyme with thiolase activity involved in peroxisomal beta-oxidation. Its primary role is in the degradation of very long-chain fatty acids (VLCFA) and branched-chain fatty acids such as phytanic and pristanic acid. In the current study, we reported the case of a patient who presented with episodic psychosis, which was determined to be caused by a novel SCP2 splicing mutation.

Ethics approval was obtained from the Second Xiangya Hospital, Central South University (Changsha, China). Written informed consent was obtained from the patient and his family members for their enrollment. A 48-year-old male was admitted to our hospital thrice between 2012 and 2017 due to episodic psychosis. During each attack, he experienced delusions, irritability, aggressive behavior, bursts of uncontrollable laughter, crying, and talking to himself. Each episode was triggered by an acute upper respiratory tract infection. He was the third child of healthy, non-consanguineous parents with no family history of relevant conditions. The patient had experienced stuttering and tremors in his lips and hands for as long as his son could remember. Physical signs were the same during each episode. Examination revealed confusion, restlessness, and disorientation to time, person, and place, with normal limb muscle strength, brisk deep tendon reflexes, positive bilateral palmomental reflex, sucking reflex, and Babinski's reflex. On each occasion, cranial magnetic resonance imaging (MRI) revealed symmetrical T2 hyperintense signals in the thalamus, mesocephalon, and pons without gadolinium enhancement (see Figure 1). The cerebrospinal fluid (CSF) showed no abnormalities. No antibodies were detected for autoimmune encephalitis, paraneoplastic neurological syndromes, and rheumatologic disorders. Ceruloplasmin, lactic acid, free carnitine, acylcarnitines, amino acids in the blood, and organic acids in the urine were all within normal ranges. Nerve conduction studies and needle electromyography showed no abnormalities. The patient was previously diagnosed with viral encephalitis, cerebral infarction, or mitochondrial encephalopathy. He received appropriate treatments, such as antiviral and antiplatelet therapy, during each hospitalization. Psychiatric symptoms gradually improved after 3–6 months of treatment with antipsychotic drugs such as olanzapine or quetiapine. Between episodes, the patient was able to care for himself and engage in communication with others independently.

In January 2018, the patient was readmitted to the hospital for continuous generalized tonic-clonic seizures (GTCS) that lasted 18 h without recovery between seizures. The GTCS occurred every 10 min, with each seizure lasting 1–2 min. Upon admission, he presented with confusion. The physical examination was limited due to poor cooperation. Pristanic acid concentration was slightly elevated at 0.62 μmol/L, just above the control range (<0.60 μmol/L), while VLCFA and phytanic acid were within the standard limit. Cranial MRI revealed abnormalities consistent with prior findings.

Whole-exome sequencing of the proband revealed a homozygous splicing mutation, c.674 + 1G > C, in SCP2 (NM_002979.5) in chr1:53442442 (hg19). Sanger sequencing confirmed the candidate mutation in the proband and his family members. The proband's father and sisters were heterozygotes at this position (see Figures 2A, B). RNA sequencing identified two outlier junctions in the SCP2 cluster, providing support for the skipping of the eighth exon (p = 4.81E-12, FDR = 0, and p = 1.31E-4, FDR = 0.008) (see Figures 2C, D). At the mRNA level, cDNA analysis validated the aberrant splicing pattern between the sixth and ninth exons in the patient's sample through the agarose gel electrophoresis of reverse transcription polymerase chain reaction amplicons (RT-PCR) product (see Figure 2E). Sanger sequencing of the RT-PCR product confirmed the exon 8 skipping event in the patient (see Figure 2F). The eighth exon has a length of 87 base pairs. This mutation results in the loss of 29 amino acid residues in the patients' SCPx protein. The allele frequency is approximately 0.00001992 in the gnomAD database. In the case of SCP2, loss of function is a recognized disease mechanism. The variant c.674 + 1G > C in SCP2 was classified as “pathogenic” based on the ACMG guidelines.

The patient's seizures were effectively halted with diazepam, and the psychiatric symptoms gradually improved. Subsequently, the patient was discharged while being placed on a phytanic acid-restricted diet.

SCPx deficiency, a rare autosomal recessive monogenic metabolic encephalopathy, has been reported in only two patients. One patient presented with leukoencephalopathy with clinical features such as slowly progressive dystonia, stutter, and motor neuropathy (2). The other patient developed hand clumsiness in his 30s, followed by gait disturbance and deafness (3). The index patient displayed episodic psychobehavioral disturbances, stutter, tremors, and epilepsy. MRI findings were consistent among all three patients, revealing symmetrical thalamus and brainstem lesions without gadolinium enhancement. As summarized in Table 1, these shared clinical features in SCPx deficiency include stutter, tremors, and symmetrical lesions in the thalamus and brainstem without gadolinium enhancement (see Table 1). Importantly, our patient first presented with episodic psychosis and epilepsy in SCPx deficiency patients highlighting the necessity for clinicians to consider the SCP2 variant during the etiological examination of individuals presenting with episodic psychosis and epilepsy.

Patients in the literature exhibited elevated pristanic acid levels, whereas the index patient showed a mild increase. Mutations in HSD17B4, which resulted in less structural damage to the D-bifunctional protein, were associated with a milder clinical and biochemical presentation (4). The D-bifunctional protein is situated upstream of SCPx in peroxisomal beta-oxidation. In our patient, the deletion of amino acid residues due to exon skipping occurs within a relatively conserved region of the protein, and this deletion region intersects with the thiolase_N domain (see Figures 2G, H). The function of the thiolase may be impaired but remains partially functional.

Intriguingly, episodic psychosis in the index patient typically follows infections, indicating that “crises” in SCPx deficiency may be provoked by factors such as infections or extended fasting, similar to certain metabolic encephalopathies, such as isolated methylmalonic acidemia (5).

The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author.

The studies involving humans were approved by the Second Xiangya Hospital, Central South University (Changsha, China). The studies were conducted in accordance with the local legislation and institutional requirements. The participants provided their written informed consent to participate in this study. Written informed consent was obtained from the individual(s) for the publication of any potentially identifiable images or data included in this article.

HT: Formal analysis, Writing—original draft. YL: Software, Writing—review and editing. ZT: Data curation, Writing—review and editing. JT: Investigation, Writing—review and editing. JF: Investigation, Supervision, Writing—original draft.