Discussion
CPT1A deficiency is a rare metabolic disease that affects fatty acid oxidation (FAO), and in the majority of cases, patients are diagnosed only after the appearance of clinic symptoms. Most patients present these symptoms by the age of 2 years with hypoketotic hypoglycemia induced by fasting or illness [
5]. This is usually accompanied by liver dysfunction; transient lipemia and renal tubular acidosis may also be present [
1]. As our patient underwent the newborn screening at the age of 3 days, indicators of CPT1A deficiency, namely, increased free carnitine and a significantly increased C0/(C16 + C18) ratio, were detected early. The diagnosis of CPT1A deficiency was confirmed by gene sequence analysis. Dietetic management and avoidance of prolonged fasting were recommended to improve the patient’s clinical outcome [
5]. Therefore, our patient developed normally, without severe metabolic crisis, till date. Indicate that early recognition of this disease is crucial for prognosis.
CPT1A deficiency is caused by mutation in the gene encoding
CPT1A. Analysis of
CPT1A is necessary for accurate diagnosis. So far, more than 30 mutations in
CPT1A, responsible for the CPT1A deficiency, have been identified [
6]. Our patient carried two missense mutations c.2201 T > C (p.F734S), previously reported in one Chinese patient [
4], and c.1318G > A (p.A440T), a novel mutation. The amino acid residue at 734 and 440 in CPT1A is highly conserved in bovine, chicken, chimpanzee, goat, horse, pig, rat, and macaque (Fig.
1I), suggesting that these loci play key roles in CPT1A normal function. According to prediction software analysis these mutations do not appear to be polymorphisms, but are more likely to be disease-causing mutations.
As we have listed the CPT1A mutations reported so far, based on the geographic region in Table
1. Most mutations seem to be unique or restricted to only a few pedigrees, except c.2129G > A and c.1436C>T [
2]. While c.2129G > A (p.G710E), a homozygous mutation associated with disease severity, is mainly found in Alaskan and Hutterite populations in the USA [
19]. c.1436C > T mutation (p.P479L) was more common in northern Canada, Greenland, Colombia, as well as the native Alaskan population [
20]. Most affected individuals in these populations are homozygous for this variant [
20]. p.P479L pathogenic variant is generally regarded as non-pathogenic with relatively high residual enzymatic activity but still associated with infant mortality [
18,
21]. Exon and multi exon deletions are rarely reported [
17]. The incidence of this disorder appears to be quite low in other regions. The true meaning of this variation in regions remains unknown. To date, only two cases of CPT1A deficiency have been reported in China [
4,
8], and both were diagnosed after the patients (> 1 year old) exhibited symptoms of hypoglycemia followed by diarrhea and fever. Moreover, there is almost complete genetic heterogeneity of disease-causing
CPT1A variations with each affected family demonstrating novel variation(s) of
CPT1A [
1]. Therefore, analysis of the entire
CPT1A is required to confirm an abnormal newborn screen and the disease-causing nature of the abnormal genotypes needs to be carefully interpreted [
7,
9]. As p.F734S mutation has been reported once in a Chinese patient with heterozygous gene mutation, it may be a unique to Chinese lineage.
Table 1
Reported CPT1A Pathogenic Variants
Alaska | c.1436C > T; | a | |
China | c.281 + 1G > A/IVS2_IVS5del; c.1787 T > C/c.2201 T > C | 2 | |
Korean | c.837_838ins(T)/c.947G > A | 1 | |
Denmark | c.167C > T | 1 | |
Finland | c.1364A > C; c.1364A > C/c.1493A > C; c.1463C > T | 6 | |
Japan | c.1339C > T/c.2156G > A; c.96 T > G/c.1079A > G; 2027–2028 + 2del; c.1425G > A/c.1494 T > G | 4 | |
Netherlands | c.1737C > A; c.478C > T; c.1600delC; c.1361A > G | 4 | |
American | c.1393G > T; c.1027 T > C; c.478C > T; c.946C > G/?; c.986C > T; c.1163 + 1G > A; c.823G > A/c.912C > G; c.367C > T; c.2129G > A# | 8 + b | |
France | c.298C > T; C.1241C > T/1493A > G; IVS14 + 3 kb; c.1876-1G > A | 4 | |
Indian | c.1069C > T/c.1451 T > C | 1 | |
Different mutations lead to different structural and functional changes. Missense mutations p.A275T, p.A414V, and p.Y498C of
CPT1A were located away from the active site and mostly affected the stability of the protein itself and/or of the enzyme–substrate complex which exhibited decreased catalytic efficiency. In contrast, mutants p.G709E and p.G710E affect glycine residues, which are critical to the structure of the hydrophobic core of the catalytic site and the chain length specificity of the CPT isoform, which greatly impair the catalytic function of CPT1A, without affecting enzyme localization and stability [
22]. Mutations like p.R357W, p.L484P, and p.C304W are associated with decreased protein stability. p.C304W, p.P479L, and p.delR395 were found to inactivate CPT1A [
18]. The p.P479L variant affects the malonoyl-CoA binding site of the enzyme, resulting in a 25% ~ 50% decrease in CPT1A activity. Another study found that mutant p.E360G caused a decrease in CPT1A protein levels [
11]. Mutations in conserved arginines and tryptophans of CPT1A have been reported to reduce enzyme activity, such as Arg388, Arg451 Trp391 and Trp452. Overall, all CPT1A mutations that lead to loss of function or stability are present in the C-terminal catalytic domain (123–773 aa) [
23]. Our patient were missense mutations causing p.F734S and p.A440T replacement. Using 3-dimensional modeling it was demonstrated that the mutation p.F734S and p.A440T may change the spatial structure which may affect protein function.
Newborn screening programs, which allow early detection of metabolic markers in dried whole blood spots when the newborn is catabolic, are therefore very important [
3]. Newborn screening for CPT1A deficiency is now mandatory in 32 states of the USA and available in 16 more states and 5 Canadian Provinces [
24]. In Italy, since 2016, extended neonatal screening has been mandatory throughout the country for about 40 inherited metabolic diseases [
25]. However, screening for CPT1A deficiency is not included in the newborn screening program in every province in China. The routine neonatal metabolic screening programs include phenylketonuria, congenital hypothyroidism, hereditary glucose-6-phosphate dehydrogenase deficiency, congenital adrenal hyperplasia, thalassemia, and neonatal hearing screening. Since 2016, Central China (Hubei Province) newborn screening program has included screening for disorders of fatty acid oxidation using MS/MS, and more than 120,000 newborn children have been tested so far. The MS/MS scanning(API3200MD,AB, America) method we used was mutiple reaction monitoring(MRM). However, only five large neonatal screening centers have been set up so far in Hubei Province, and the feedback mechanism are not perfect in some regions, Which may lead to prolonged screening time and delay in diagnosis. If abnormal results occur, the child will be referred to a pediatric endocrinologist for further examination.
CPT1A deficiency is characterized by significant decrease in the synthesis of all acyl carnitine species, as well as increased levels of free CO and C0/(C16 + C18) on newborn screen blood spots. The MS/MS is used to detect elevated free carnitine to C16 + C18 ratio, which is characteristic of CPT1A patient [
3]. Urine organic acids show elevated levels of dodecanodi acid in acute crisis and subsequent days [
13]. In this case, the results of urine organic acid were normal, possibly the patient was not in the acute stage. In this case, plantar blood was collected 3 days after birth, and abnormalities came out at 30 days old, which is a long and dangerous time. The time of newborn screening test in our province should be improved.
According to the data from newborn screening programs in Australia, Germany, and the USA the incidence of CPT1A deficiency may be as low as 1:750,000 to 1:2,000,000 [
26]. Alaska infants have a high prevalence of CPT1A c.1436C > T mutation in newborn screening program [
27]. There is evidence suggests that homozygous infants with this variant have impaired fasting tolerance [
28] and increased risk of infant mortality [
7]. Five of 152 homozygous infants died for c. 1436 c > T mutation, two of 219 heterozygous infants died, and zero of 245 non-carriers died. In a study of Arctic populations with whole-genome high-coverage sequence, the CPT1A variant was identified as deleterious and associated with increased infant mortality in surrounding Arctic populations [
21]. There are only two cases without death in China so far. The present case is the first presymptomatic CPT1A deficiency case detected through newborn screening in China. As neonatal MS/MS screening becomes more comprehensive across the country, it is possible that the detection rate will be higher.
CPT1A deficiency is a long-chain fatty acid oxidation disorder. Most individuals have a residual enzyme activity of 1–5% [
23]. When energy demand increases, clinical manifestations usually occur in individuals with concurrent fever or gastrointestinal disease; Symptoms usually appear quickly. Prolonged fasting should be avoided or a sufficient level of glucose should be supplied, especially during periods of fever or gastrointestinal illness. Potentially hepatotoxic drugs such as valproate and salicylate should not be given, even though adverse pharmacological reactions have not been reported in individuals with CPT1A deficiency [
2]. Previous reports has indicated that following a strict dietary regimen allows the CPT1A-deficient infant to lead a healthy life with normal growth and development [
3]. Consistent with this reports, our patient was diagnosed at an early age, received timely intervention, and showed a normal growth trend. However, There may not be clinical trials for this disorder. The newborn metabolic screen is important for early diagnosis and treatment. Considering the simplicity of this method, it can be implemented across the country. Moreover, in the present cases, genetic counseling was recommended for the parents, should they wish to have another baby.
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