Yuqi Yang
Shu hong Jiang1
Ying Wang
Bin Yu- 1Changzhou Maternity and Child Health Care Hospital, Nanjing Medical University, Changzhou, China
- 2Lianyungang Maternal and Child Health Hospital, Yangzhou University, Lianyungang, China
Beta-ketothiolase deficiency (BKTD) is an autosomal recessive disease caused by a defect of mitochondrial acetoacetyl-CoA thiolase. Beginning in 2014, we carried out newborn screening by tandem mass spectrometry (MS/MS) followed by next-generation sequencing (NGS) and identified two infants with BKTD among 203,750 newborns born in Jiangsu Province, China. Both infants showed the characteristic chemical abnormalities of BKTD. We used NGS to confirm variants in the ACAT1. Patient 1 had the compound heterozygous variants c.721dupA and c.928G > C. Patient 2 had compound heterozygosity for the c.238+1G > A and c.1163G > T variants. c.721dupA, c.928G > C and c.1163G > T were suspected to be likely pathogenic, whereas c.238+1G > A was determined to be pathogenic. None of the four variants have been reported in the literature. Patient 1 presented with onset of metabolic acidosis and neonatal hypoglycemia 8 days after birth, whereas patient 2 was detected through neonatal disease screening but had no clinical manifestations. These findings contribute to our understanding of the clinical characteristics and genetic basis of BKTD.
Introduction
Beta-ketothiolase deficiency (MIM 203750) occurs due to a mitochondrial acetoacetyl-CoA thiolase (T2; EC2.3.1.9) defect caused by mutation of ACAT1 (NG_009888, NM_000019.3), leading to the abnormal metabolism of isoleucine and ketone. The incidence of BKTD is very low. Since its first description in 1971, about 135 cases have been reported (Fukao et al., 2019). Most patients have no obvious clinical manifestations in the early postnatal period. The age of onset is usually 6 to 18 months (Abdelkreem et al., 2016; Nguyen et al., 2017), and patients grow well before the first attack. Timely intervention and treatment before the first episode can enable full recovery or prolong the period until symptoms develop. The clinical manifestations of BKTD are non-specific and variable, with the most common clinical feature being acute ketoacidosis (Sass, 2012). Because most patients with BKTD do not exhibit significant clinical symptoms, newborn screening by tandem mass spectrometry (MS/MS) may be the only approach for early detection.
Since 2014, we have performed newborn screening for BKTD by MS/MS followed by next-generation sequencing (NGS) for genetic diagnosis. The study design and protocol were reviewed and approved by the Ethics Committee of the Changzhou Maternity and Child Health Care Hospital, affiliated with Nanjing Medical University (No. 201502). Written informed consent was obtained from all of the infants’ parents before newborn screening. Over 5 years, we screened 203,750 infants and diagnosed two cases of BKTD, as described herein.
Case Presentation
Patient 1
A woman gave birth to a full-term infant of 3800 g by cesarean section at a gestational age of 38+6 weeks. The boy was 49 cm long, with a head and chest circumference of 33 and 32 cm, respectively. Apgar scores in the first and the fifth minutes were both 9. The mother and her spouse had no family history of BKTD. Their first child was a phenotypically normal girl. This boy was admitted to the hospital 8 days after birth with rapid breathing, poor reaction, and spitting for 2 days. A hospital physical examination found a lack of alertness, paleness, and shortness of breath but no cyanosis. Pulmonary auscultation revealed crackles in both lung fields. He also had reduced muscle tone and swelling of the right heel. In auxiliary examinations, the results of routine blood examination, urine tests (including urine ketone body test), and tests for hepatic and renal function were normal. Values of biochemical parameters in the cerebrospinal fluid were also normal. Cerebrospinal fluid bacterial culture was negative. A blood gas analysis indicated metabolic acidosis and neonatal hypoglycemia with an arterial pH of 6.783, PCO2 of 16.3 mmHg, PO2 of 315 mmHg, lactic acid of 2.5 mm/L, BE of –30.4 mmol/L, and glucose level of 2.1 mmol/L. A chest radiograph showed increased lung markings.
Written informed consent was obtained from the patient’s parents before screening for participation in and publication of this case report. The baby received newborn screening by MS/MS 3 days after birth. The concentrations of malonylcarnitine+3-hydroxybutyrylcarnitine (C3DC+C4OH), methylmalonylcarnitine+3-hydroxyisovalerylcarnitine (C4DC+ C5OH), and tiglylcarnitine (C5:1) exceeded the cut-off values (Table 1). Urinary organic acid analysis by gas chromatography-mass spectrometry (GC-MS) showed increased levels of 2-methyl-3-hydroxybutyric acid and methylcrotonylglycine at 44.14 (reference range, 0.0–0.3) and 9.8 (reference range, 0.0–0.1), respectively. The MS/MS results and urine organic acid levels were highly indicative of BKTD.
Table 1. Biochemical criteria and clinical manifestations.
We used NGS to identify pathogenic mutations. The baby had the complex heterozygous variants c.721dupA (p.Thr241Asn fs*14), located in exon 7, and c.928G > C (p.Ala310Pro), located in exon 9 in the ACAT1. We also found the heterozygous mutations c.804del in SLC25A20 and c.799C > T in HMGCL. We verified the mutations in ACAT1 in the baby and his family members by Sanger sequencing. The c.721dupA variant was inherited from his father, and the c.928G > C variant was inherited from his mother. His sister only inherited c.721dupA from the father and had no clinical manifestations as an asymptomatic carrier (Figure 1). We used the Genome Analysis Toolkit1 to identify the mutation sites in the target sequence and Annovar2 to annotate all mutation sites within the public database. The influence of the mutations on protein function was predicted according to the frequency of the mutations in the normal population, the conservation of the mutated sequence, and the amino acid changes caused by the mutations as well as their locations in the protein structure. Finally, combined with the sample’s own situation, we inferred the pathogenicity of each mutation based on the ACMG standards and guidelines. We determined that the variants in patient 1 may affect the function in the ACAT1 protein. c.721dupA and c.928G > C were identified as likely pathogenic (Table 2).
Figure 1. The variants of ACAT1 gene in patient and his family.
Table 2. Characteristics of disease-causing genetic variants.
At the time of diagnosis, we treated the initial clinical symptoms, such as neonatal pneumonia, neonatal hypoglycemia, and metabolic acidosis. Specific measures included oxygen inhalation therapy, correction of acidosis with sodium bicarbonate, relief of heart burden using furosemidum, infection control, and fluid replacement therapy. These treatments substantially relieved the child’s symptoms. After a definitive diagnosis of BKTD, the patient was administered enough glucose to reduce protein breakdown and carnitine to reduce excessive acid metabolites. After discharge, the patient was instructed to limit protein intake [1–2 g/(kg⋅d)] and avoid hunger and was administered oral l-carnitine [dosage of 50–100 mg/(kg⋅d)]. The patient was followed up every 3 months, and the dosage of l-carnitine was adjusted according to the levels of C3DC+C4OH, C4DC+C5OH, and C5:1. The boy is now 15 months old. No serious complications have occurred during the year of follow-up.
Patient 2
Patient 2 was 50 cm in length at birth, with a head circumference of 33 cm and chest circumference of 32 cm. His Apgar scores at 1 and 5 min were both 9. Written informed consent was obtained from the patient’s parents before screening for participation in and publication of this case report. Based on newborn screening by MS/MS, C3DC+C4OH and C4DC+C5OH levels and the C5:1 ratio in the blood were elevated, similar to the results for patient 1. High levels of 2-methyl-3-hydroxybutyric acid were also detected in his urine by GC-MS (Table 1). We found two variants in the ACAT1, with mutations c.238+1G > A and c.1163G > T (P.Gly388Val) (Table 2). The c.238+1G > A mutation of ACAT1 is a splice site mutation, altering the nucleotide at position 1 of the 5′ end of intron 2. According to ACMG guidelines, classical splice-site mutations disrupt gene functions, e.g., by an inability to transcribe or synthesize the corresponding products (Richards et al., 2015). c.1163G > T is a missense mutation predicted to be likely pathogenic. Unlike patient 1, patient 2 did not have any clinical manifestations. His parents refused further genetic analysis and follow-up visits, and thus additional clinical information on the child is lacking. We did not intervene medically, other than recommending close follow-up. The boy has not yet exhibited severe clinical manifestations.
Discussion
It is generally believed that BKTD lacks specific clinical manifestations. Most affected children suffer from diseases caused by fasting, fever, infection, and other issues, which result in sudden ketoacidosis (Thummler et al., 2010; Hori et al., 2015). The age of first onset of ketoacidosis in most cases is 6 to 18 months. Fukao (Fukao et al., 2014) claimed that mitochondrial medium-chain 3-ketoacyl-CoA thiolase (T1) can partially compensate for the T2 deficiency. Ketogenic triggers, such as prolonged fasting, infection, and protein-rich foods, may disrupt this compensation and precipitate acute ketoacidosis. Frequent feeding, protective maternally acquired immunoglobulins, and the relatively low protein contents of breast and ordinary milk formulas reduce the risk of ketogenic triggers (Nguyen et al., 2017). Therefore, the sooner affected children receive intervention after birth, the better the control of the disease.
Some BKTD patients present with neurological symptoms before the onset of ketoacidosis (Buhas et al., 2013), whereas others exhibit other metabolic abnormalities, such as hypoglycemia, hyperglycemia, or high blood ammonia. In this study, patient 1 developed severe metabolic acidosis and hypoglycemia at 8 days after birth due to a pulmonary infection. The age of onset was earlier than the average reported in the literature. Neonatal onset of T2 deficiency is very rare. Fukao et al. (2019) reported only two cases with neonatal onset out of 135 patients with T2 deficiency. Acidosis, hypoglycemia, and unconsciousness occurred in one case during the first episode, similar to that observed in patient 1 in this study. Ketonuria is usually evident in patients with BKTD during acute ketoacidosis; however, patient 1 had no detectable ketonuria. This may occur if urinary testing was performed after correcting the metabolic derangements. Another possible cause may be the coexistence of another inherited defect in ketogenesis or beta–oxidation. However, NGS did not reveal biallelic variants in relevant genes. Only one SLC25A20 variant (c.804del) was identified in patient 1; if an additional SLC25A20 variant was detected, we might attribute the absent ketonuria in this patient to a coexistent carnitine-acylcarnitine translocase deficiency. Secondary carnitine deficiency that may suppress beta-oxidation might be another explanation (Aghamaleki et al., 2019). However, the coexistence of secondary carnitine deficiency in patient 1 is unlikely because he did not have low carnitine levels.
According to current reports, most children with BKTD exhibit abnormalities in urinary organic acid and blood acyl carnitine. Meanwhile, some studies have reported only subtle abnormalities, even during acute episodes (Fukao et al., 2012). The detection of enzyme activity in fibroblasts using “coupled assay” test cannot be used to distinguish T2 deficiency from 2-methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency (Gibson et al., 1992). Some patients with residual enzyme activity may also be missed (Zhang et al., 2004). T2 and MHBD deficiencies may result in similar urinary organic acid abnormalities (Fukao et al., 2014). Therefore, BKTD cannot be diagnosed based only on urine test results or the detection of enzyme activity. Fortunately, there are other ways to identify T2 and MHBD deficiency. For example, 2-methylaceoacetate is only detected in T2 deficiency, and the potassium-dependent AA-CoA thiolase assay gives a normal result in cases of MHBD deficiency (Haapalainen et al., 2007). Unfortunately, the results of these tests were not available in our patients, and this represents a limitation of our study. Beyond that, genetic testing is another important way to distinguish T2 and MHBD deficiencies. This was exactly what our research uses.
Newborn screening is highly effective for the detection of diseases in children who lack clinical symptoms. In the 1990s, the categories of inherited metabolic diseases included in screening were expanded by the introduction of MS/MS (Frazier et al., 2006). Likewise, NGS enables the sequencing of hundreds of thousands to millions of DNA molecules simultaneously and can be used to detect variations in disease-causing genes simply and accurately. In China, the combination of MS/MS and NGS is considered to be a superior method for newborn screening. Beginning in 2014, we screened for diseases in this way and have successfully diagnosed and intervened in many metabolic diseases (Yang et al., 2019). In this study, MS/MS results suggested the possibility of BKTD, but abnormalities in blood acylcarnitine are not specific to BKTD. Therefore, we performed related auxiliary examinations based on clinical manifestations including urine gas chromatography, a blood biochemistry test, and blood glucose test. At the same time, we performed genetic testing and mutation site validation on the children and their families to confirm BKTD. Both patient 1 and patient 2 had compound heterozygous mutations of ACAT1 (c.721dupA and c.928G > C in patient 1; c.238+1G > A and c.1163G > T in patient 2), none of which have been reported in the literature. Of course, normal newborn screening does not absolutely exclude BKTD.
The ACAT1 is located on chromosome 11q22.3 to q23.1. It is 27 kb in length and is composed of 12 exons and 11 introns (Kano et al., 1991). Variations of ACAT1 in patients are diverse, and genotypes are not related to clinical manifestations (Nguyen et al., 2017). In Asia, it has been reported that the mutation frequency of c.1124A > G in the Chinese population is relatively high, whereas c.266G > C is the mutation with the highest frequency in Vietnam (Fukao et al., 2010) and c.578T > G is the most common mutation in India (Abdelkreem et al., 2017). Since the pathogenicity of the four new mutations detected in this study was predicted by software (e.g., SIFT, PolyPhen2, PROVEAN, and Mutation Taster), their pathogenicity should be further confirmed by in vitro protein functional expression assays. Meanwhile, we are submitting the four novel ACAT1 variants to the public database (ClinVar).
Previous reports have indicated that the incidence of BKTD is less than 1 per 1 million newborns. However, data from newborn screening from many countries has shown that the incidence is higher than previously estimated (Sarafoglou et al., 2011). Since 2014, our laboratory has screened more than 200,000 newborn babies and identified two cases, resulting in an incidence of BKTD of 1:101,875. China has not yet popularized MS/MS screening, and therefore reliable data on the incidence of BKTD among the Chinese population is lacking. However, an increasing number of newborn screening centers in China have begun performing this test (Han et al., 2007; Sun et al., 2011; Guo et al., 2018; Yang et al., 2018). We believe that future studies on the Chinese population will provide useful information and a clearer understanding of BKTD.
Ethics Statement
The study design and protocol were reviewed and approved by the Ethics Committee of the Changzhou Maternity and Child Health Care Hospital, Nanjing Medical University (No. 201502). We obtained written informed consent for genomic analysis from the parents of the baby and the mother of the patient provided written informed consent for the publication of this case report.
Author Contributions
BY and LW carried out the assays and participated in the study design. YY, SJ, SL, XH, and YW carried out clinical consultations, laboratory tests, and performed the statistical analysis. BY conceived the study, participated in its design and coordination and helped draft the manuscript.
Funding
This study was funded by the Key Research and Development Plan Project of Jiangsu Province (BE2017650 and BE2018677), Changzhou Science and Technology Support Project (Social Development CE20175021), and Jiangsu Maternal and Children Health Care Key Discipline (FXK201754).
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
We thank all of the project participants for their contribution to the study.
Footnotes
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Keywords: newborn screening, inborn errors of metabolism, tandem mass spectrometry, beta-ketothiolase deficiency, next-generation sequencing, ACAT1
Citation: Yang Y, Jiang S, Liu S, Han X, Wang Y, Wang L and Yu B (2019) Two Infants With Beta-Ketothiolase Deficiency Identified by Newborn Screening in China. Front. Genet. 10:451. doi: 10.3389/fgene.2019.00451
Received: 23 January 2019; Accepted: 30 April 2019;
Published: 15 May 2019.
Edited by:
Andrew Landstrom, Duke University, United StatesReviewed by:
Sarah H. Elsea, Baylor College of Medicine, United StatesElsayed Abdelkreem, Sohag University, Egypt
Copyright © 2019 Yang, Jiang, Liu, Han, Wang, Wang and Yu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Bin Yu, eWJjejA1MTlAMTYzLmNvbQ==