Molecular diagnosis of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Congenital adrenal hyperplasia is an autosomal recessive group of diseases. 21-Hydroxylase deficiency (21OHD) is the most frequent cause of CAH accounting for 95–99% of cases [1‐3], and is the result of mutations in the CYP21A2 gene [4]. The CYP21A2 gene is located in the highly polymorphic region of the major histocompatibility complex (HLA), on the short arm of chromosome 6, locus p21.3, accompanied by a CYP21P pseudogene, with which it has a 98% homology. Moreover, they are located in tandem after the 3 ‘terminal portion of the 2 genes that code for the fourth complement component (C4A and C4B) [2, 4].

Like all recessive diseases, patients with CAH have both alleles (maternal and paternal) affected, and only 1% is the result of a spontaneous mutation. Gene abnormalities are variable and include anything from point mutations to large deletions. The clinical phenotype is the result of the combination of these abnormalities in the two CYP21A2 alleles with the least affected allele usually determining the phenotype [3‚ 4].

Molecular analysis of the CYP21A2 gene in patients with 21OHD, in North American and European populations, has shown that about 25% of these patients present macrodeletions of approximately 30 Kb, which include not only much of the 5′ region of the CYP21A2 gene, but also all of the C4B gene and 3′ region of the CYP21P gene, or CYP21A2 gene macroconversions in a similar way to CYP21P. The remaining 75% have gene microconversions or point mutations (PM) [5, 6]. The most frequent PM described in the classical forms are: I172N, R356W and G318X, a change from C to G in intron 2 which produces a splicing acceptor site 12 bases upstream of the normal splicing acceptor site, called ln2, a deletion of 8 bp in exon 3 that generates a shift in the reading frame and the appearance of a premature stop codon, called Ex3, and three T substitutions for A in codons 234–238, that determine a change in the sequence of Lle-Val-Glu-Met amino acids by Asn-Glu-Glu-Lys, called Cluster Ex6 [6, 7]. In the non-classic (NC) form, the most frequent PM described are P30L and V281L, respectively [8, 9].

On the other hand, deletions of the CYP21P gene associated with deletions of the C4A or B gene have been described in the normal population [8] and duplications of the CYP21P and C4B gene are frequently associated with NC 21OHD. Given the high homology between the CYP21 genes and the complexity of the gene locus, the study at the molecular level is difficult. Thus, it is necessary to implement appropriate methodologies and strategies.

CYP21A2 gene mutations have been studied in different ethnic groups, and it has been shown that a small number of mutations is responsible for the majority of 21OHD cases [8‐11]. Thus, identifying only these few mutations can be used in a simplified and cheaper CYP21A2 mutation analysis which may be more accessible in places with economical restrictions.

In 2005, the neonatal screening program was established in Cuba [12, 13], using 17-hydroxyprogesterone (17OHP) detection in dry blood on filter paper through the neonatal UMELISA Kit [14]. Its main objectives are early diagnosis of the classic form in both genders, to prevent life-treating salt-wasting crisis and to avoid incorrect sex assignment in the newborn.

The CYP21A2 gene analysis is a useful complement to predict phenotype as well as confirming the diagnosis [15]. It is also important in situations where the 17OHP concentrations are unclear and in prenatal diagnosis when a child in a family is affected. Genotype may also predict long-term outcomes [16‐18].

Thus, the aim of the current study was to characterize the genotype in patients diagnosed clinically with 21OHD and identifying the most frequent mutations in the Cuban population.

A cross-sectional descriptive study was performed of all patients diagnosed clinically with 21OHD from January 2000 to December 2018 at the National Institute of Endocrinology, Havana, Cuba. The local ethical committee approved the study and informed consents were obtained.

For the molecular analysis of the CYP21A2 gene, a protocol designed and approved by the National Center for Medical Genetics was used. The first stage used a 2-phase Polymerase Chain Reaction (PCR) and in the second stage, 5 different point mutations were detected (Intron 2, 8 bp Deletion, G318X, I172N and P30L). Characteristics of the mutational analysis in the CYP21A2 gene are shown in Table 1.

A total of 55 patients underwent CYP21A2 gene mutation analysis to determine the presence of five common point mutations and these were identified in 31 patients (56%), of which 28/38 (74%) with classic forms and 3/16 (19%) NC form. Table 2 present the clinical characteristics of the phenotype groups.

In relation to the familial reproduction history, 23 (42%) identified some pathological elements, 10 (19%) infertility, 9 (16%) had been referred for spontaneous abortions, 7 (13%) hirsutism, 5 (9%) had a history of known CAH diagnosis in first-degree relatives, 2 (4%) neonatal death of unknown cause, 2 (4%) polycystic ovary syndrome and 1 (2%) atypical genitalia of unknown cause. No consanguinity was present. When the studied patients were analyzed in detail, 22 (71%) detected 1 mutation, 5 (16%) 2 mutations, 3 (10%) 3 mutations and 1 (3%) 4 of the investigated mutations. The details of the five point mutations studied are specified in Table 3.

The most frequent PM in the SW forms was Intron 2 (9/15, 60%), 4 of them in homozygosis, 2 in heterozygosity and 3 in compound heterozygosity with other mutations (Homo I172N Hetero Intron 2, P30L and 8pb (1) and Hetero Intron 2 P30L and 8 bp (2)). Also in the SV form Intron 2 mutation was the most frequent (9/11, 82%), present in 3 of those in homozygous, 3 in heterozygosis and the rest in compound heterozygosity (Hetero Intron 2 and I172N (1), Hetero Intron 2 and G318X (1) and Hetero Intron 2 and 8 bp (1)). Finally, in the NC form (all diagnosed with the ACTH stimulation test with measurements of 17OHP levels) the causal mutation was identified in 3/16 patients (19%), 2 heterozygous for G318X and 1 heterozygous for Intron 2. Figure 1 shows the distribution of the identified mutations according to the number of alleles affected, in each of the clinical presentation forms. The most frequent mutation was Intron 2, followed by G318X, deletion of 8 base pairs, and I172N and P30L (Fig. 2).

The presence of single chromosome abnormalities in a group of patients suggest that family members should be studied. Due to laboratory limitations, only in 10 families both parents were studied and in 4 more families only one parent (Table 3). When analyzing the 10 heterozygous patients, girls predominated (8/10) and 4 of the patients presented with classic forms (Table 4). According to the genotype, they were distributed into three groups, of which G318X was present in 7 of 10 patients (70%). The segregation of the mutation was 50/50 maternal/paternal.

CAH is the most important cause of 46,XX disorder of sexual development (DSD), constituting 87.5% of all 46,XX DSD in Cuba [19, 20]. Newborns screening for CAH in Cuba [13] was an important milestone for the early hormonal diagnosis but genetical diagnosis was still an unsolved problem. Molecular genetic studies in CAH started many years ago [9]. In general, genetic studies are very expensive, which is a limitation for developing countries, such as Cuba. Based on studies on ancestry in the Cuban population [20‐24], it has been estimated that our population received a contribution of genes of European origin (72–83%), African origin (13.8–26%) and Native American origin (0.8–3.2%). These results served as a basis for reviewing the frequency of PMs identified in the Spanish population [25] and those recognized with the highest prevalence were chosen to be explore in the present investigation.

Currently, direct analysis of the gene encoding the enzyme 21-hydroxylase is possible, and the detection of gene alterations causing the disease. However, as some studies have shown [26], direct analysis can sometimes provide limited information due to the presence of complicated rearrangements between CYP21A2 and CYP21P, which make it difficult to determine whether the individual is affected or not.

More than 200 mutations have been described, PMs, small deletions, insertions and complex rearrangements of the gene. The most common mutation appears as a result of one or two types of meiotic recombination events between CYP21A2 and CYP21P: 1) misalignment and uneven crossing, resulting in large DNA deletion, and 2) gene conversion events. Apparently, they give rise to the transfer to CYP21A2 of small mutations present in the pseudogene [27, 28].

Throughout the years, the different methodologies used to study the CYP21A2 gene have increased our genetic knowledge of 21OHD [4, 9, 29]. It has been possible to find characteristic mutations in some populations [29], including unaffected individuals [30]. Therefore, molecular analysis of the CYP21A2 gene is the key to understand the etiology of 21OHD, both in basic science and in clinical diagnosis.

The economic cost of such genetic studies is a limitation for our country; hence, it was only possible to study the presence of five frequent PMs. The strategy used in this study offered encouraging results; with causal mutation being detected in more than half of the affected patients. In particular, in the group of SW patients, mutations causing severe deficit were identified in the majority. It was striking that not all of them had severe mutations in both the paternal and maternal chromosomes. In addition, in some of them, several mutations were observed on the same chromosome, so the total number of mutations detected was higher than that of the unrelated chromosomes studied. For this reason, it is important to carry out, in all cases, both the detection of large rearrangements using the Southern blot technique, and the widest possible analysis of mutations by PCR, to be able to establish an exact genotype.

The most frequent point mutation in the SW form of the Cuban population studied was the intron 2 mutation, which coincides with other studies [27, 31]. The severe G318X mutation was the second most common mutation, similar to that observed in other populations [32‐34]. In addition, the 8 base pair deletion in exon 3 was present in 3 of the SW patients, in all, in compound heterozygosity, and more frequent than others have described [30]. In all, 76% of the SW cases were characterized genetically.

Moreover, this limited methodology allowed the characterization of 12 of 18 patients (67%) with the SV form. The frequency of mutations in this phenotype was somewhat peculiar, the frequency of the Intron 2 mutation was present in 64%, much higher than that found in other populations [26, 33, 35]. In all homozygous Intron 2 patients in our study, 4 of them had the SW form and the other 3 the SV form. In some patients it may exist in a certain degree, correct processing of the messenger ribonucleic acid (RNA) [36]. The rest of the patients with SV phenotype presented a similar mutation in compound heterozygosity.

Unlike other studies [31, 37] where the P30L mutation was found with high frequency in patients with the NC form, in our population P30L was only found in 3 patients with classic form, all in compound heterozygosity, which is rare.

Regarding patients with the NC form, molecular genetic analysis allowed only the characterization in about 20% of patients. It is possible that the remaining patients had other mutations not measured in this study or new mutations that do not exist in the pseudogene. The most common mutation in the NC phenotype is V281L [38], and unfortunately, we were not able to analyze this PM. Hence, new studies to further characterize this group in our population is needed.

Of the 3 patients with NC forms, 2 presented the G318X mutation in a heterozygous state and 1 was heterozygous for Intron 2. On the other hand, the P30L mutation, which is described as frequent in NC phenotype, was not found [27, 36]. It should be noted that the 3 patients characterized presented severe mutations in heterozygosity, causing classical forms, which would not have been possible to detect without using these molecular techniques and, moreover, they pose important implications for genetic counseling in these families [39]. Considering that it is an autosomal recessive hereditary disease, it is expected that patients with enzyme deficiency, regardless of their clinical form, presented abnormalities in the 21-hydroxylase gene on both chromosomes.