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CASE REPORT article

Front. Cardiovasc. Med., 08 November 2022
Sec. Cardiovascular Genetics and Systems Medicine
This article is part of the Research Topic Case Reports in Cardiovascular Genetics and Systems Medicine: 2022 View all 15 articles

Case report: Genomic screening for inherited cardiac conditions in Ecuadorian mestizo relatives: Improving familial diagnose

\nSantiago Cadena-Ullauri&#x;Santiago Cadena-Ullauri1Patricia Guevara-RamirezPatricia Guevara-Ramirez1Viviana Ruiz-PozoViviana Ruiz-Pozo1Rafael Tamayo-TrujilloRafael Tamayo-Trujillo1Elius Paz-CruzElius Paz-Cruz1Tatiana Snchez InsuastyTatiana Sánchez Insuasty2Nieves DomnechNieves Doménech3Adriana Alexandra Ibarra-RodríguezAdriana Alexandra Ibarra-Rodríguez4Ana Karina Zambrano
&#x;Ana Karina Zambrano1*
  • 1Centro de Investigación Genética y Genómica, Facultad de Ciencias de la Salud Eugenio Espejo, Universidad UTE, Quito, Ecuador
  • 2Cardióloga ecocardiografísta, Centros Médicos Especializados Cruz Roja Ecuatoriana, Quito, Ecuador
  • 3Instituto de Investigación Biomédica de A Coruña (INIBIC)-CIBERCV, Complexo Hospitalario Universitario A Coruña (CHUAC), Sergas, Universidad da Coruña (UDC), La Coruña, Spain
  • 4Grupo de Investigación Identificación Genética-IdentiGEN, FCEN, Universidad de Antioquia, Medellín, Colombia

Introduction: Genomic screening is an informative and helpful tool for the clinical management of inherited conditions such as cardiac diseases. Cardiac-inherited diseases are a group of disorders affecting the heart, its system, function, and vasculature. Among the cardiac inherited abnormalities, one of the most common is Wolff-Parkinson-White syndrome. Similarly, hypertrophic cardiomyopathy is another common autosomal dominant inherited cardiac disease. Hypertrophic cardiomyopathy is associated with an increased incidence of Wolff-Parkinson-White syndrome; reports have suggested that it could be caused by a mutation in the protein-coding gene PRKAG2, which encodes a subunit of the AMP-activated protein kinase.

Case presentation: A 37-year-old Ecuadorian male (Subject A) with familiar history of bradycardia, cardiac pacemaker implantation, and undiagnosed cardiac conditions began with episodes of tachycardia, dizziness, shortness of breath, and a feeling of fainting. He was diagnosed with hypertrophic myocardiopathy and Wolff Parkinson White preexcitation syndrome. Furthermore, his cousin's son, an 18-year-old Ecuadorian male (Subject B), started suffering from migraine and tachycardia at any time of the day. He was diagnosed with hypertrophic myocardiopathy; his electrocardiogram showed a systolic overload. Next-generation sequencing and ancestry analyses were performed. A c.905G>A p.(Arg302Gln) mutation in the gene PRKAG2 and a mainly European composition were identified in both subjects.

Conclusion: Genetic testing is a valuable tool as it can provide important information regarding a disease, including its cause and consequences, not only for single individuals but to identify at-risk relatives. Furthermore, NGS results could guide the physician into targeted therapy. In the present case report, a missense pathogenic Arg302Gln mutation in the PRKAG2 gene has been identified in two related Ecuadorian Subjects diagnosed with hypertrophic myocardiopathy and Wolff-Parkinson-White. The variant has not been reported in Latin America; hence, this is the first report of the Arg302Gln mutation in the PRKAG2 gene in mestizo Ecuadorian subjects with mainly European ancestry components.

Introduction

Genomic screening is an informative and helpful tool for the clinical management of inherited conditions such as cardiac diseases. Thus, the results could be essential for identifying the disease causative, starting the patient early and targeting treatment, and increasing the chances of survival since there is evidence of an increased risk of sudden death in some cardiac conditions (1).

Cardiac-inherited diseases are a group of disorders affecting the heart, its system, function, and vasculature (2). In 2015, the % of deaths caused by heart disease was 20.3% for the Hispanic ethnic group in the United States (3). In Ecuador, in 2016, the first cause of death was acute myocardial infarction which constituted 9.05% of deaths (4).

Among the cardiac inherited abnormalities, one of the most common is Wolff-Parkinson-White syndrome (WPW), an autosomal dominant disease; its prevalence fluctuates between 0.68 and 1.7/1000 (5). WPW involves an abnormal atrioventricular electrical conductive with an electrocardiogram (ECG) pattern of short PR interval and prolonged QRS (6, 7). Its associated symptoms include tachycardia, such as palpitations, syncope, dizziness, and sudden death (7).

Furthermore, hypertrophic cardiomyopathy (HCM) is one of the most common autosomal dominant inherited cardiac diseases, with an estimated prevalence of 1 per 200 to 500 people in the general population (8). Recent studies suggest that approximately 20 million people worldwide are affected by HCM (just 10% of cases are identified) (810). HCM diagnosis is based on the presence of a non-dilated left ventricular hypertrophy, identified by an echocardiogram or magnetic resonance (8). At a cellular level, cardiac myocytes are hypertrophied, disorganized, and separated by fibrosis areas (11).

The HCM is associated with an increased incidence of WPW syndrome; reports have suggested that it could be caused by a mutation in the protein-coding gene PRKAG2, which encodes a subunit of the AMP-activated protein kinase (AMPK). AMPK is essential in regulating cellular ATP energy metabolism since it activates energy production and inhibits energy consumption (5, 12).

Here we report a complete genomic screening for cardiac inherited conditions of two relatives to improve early diagnosis of familial cases.

Case description

Clinical phenotype

A 37-year-old Ecuadorian male (Subject A) with familiar history of bradycardia; his father, two paternal aunts, and paternal grandmother underwent cardiac pacemaker implantation because of the bradycardia. Additionally, a cousin (father of subject B) was diagnosed with hypertrophic cardiomyopathy, and a half-brother from his father's side suffers an unknown cardiac condition (Figure 1). The patient went to the physician at the first time when he was 23 years old because of symptoms such as tachycardia, dizziness, shortness of breath, and a feeling of fainting at any time of the day. He was referred to the cardiologist, and electro and echocardiogram were performed. The diagnoses of WPW and HCM were based on the electrocardiogram, which showed a sinus rhythm with a short P-R interval accompanied by a prolonged QRS complex with a delta wave. A complete right bundle branch block with a significant increase in R wave voltages in the anterior, septal, low lateral, and high lateral (DI and aVL) regions was observed. A deep T wave inversion was identified in this same plane, and a low level in the segment ST-T V3-V6 (Supplementary Figure S1). The echocardiogram confirmed a structurally normal heart. Carvedilol was initially prescribed at a dose of 6.25 mg per day. However, four months prior to the publication of this case report, the dose increased to 12.5 mg daily.

FIGURE 1
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Figure 1. Subject A and B pedigree. Subject A and Subject B are indicated with an arrow. The family history of cardiac problems is depicted in the pedigree.

Fourteen years later after the initial diagnosis, a genomic test was performed.

Moreover, 3 years ago, his cousin's son, an 18-year-old Ecuadorian male (Subject B) with the same familiar history of cardiac conditions (Figure 1), was referred to the cardiologist after suffering from migraines and tachycardia at any time of the day, especially after a sudden movement. Subject B underwent an electrocardiogram, and the results showed a systolic overload compatible with hypertrophic myocardiopathy, no association with WPW was found. Bisoprolol was prescribed at a dose of 1.25 mg daily, and the subject reported a significant reduction in the frequency of migraines. Similar to Subject A, a genomic screening was done. The timeline regarding subject A and B is presented in Figure 2.

FIGURE 2
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Figure 2. Subject A and B timeline. The relevant data is displayed in the timeline.

Sampling and DNA extraction

Patients A and B self-identified as “mestizo” and signed the informed consent to participate in the study.

A peripheral blood sample was collected in an EDTA tube. The DNA was extracted with PureLink Genomic DNA Mini Kit (Life Technologies) according to the manufacturer's protocol (13).

The DNA quantity and purity were measured by spectrophotometry and fluorometric methods; the quality was analyzed with an agarose gel. The sample was then diluted to 5ng/μL according to the sequencing protocol.

Next-generation sequencing (NGS)

The genomic procedure was performed at Centro de Investigación Genética y Genómica, using the commercially available kit TruSight Cardio kit (Illumina), covering 174 genes (575 kb of cumulative target region size) with known association with 17 Inherited Cardiac Conditions (47 genes for Hypertrophic Cardiomyopathy). The samples were processed according to the manufacturer's protocol (14) and run for 315 cycles in MiSeq System (Illumina).

Ancestral proportion analysis

For ancestral proportion analyses, PCR amplification was done with 46 ancestral informative INDEL markers in one multiplex reaction, according to Pereira et al. (15). Fragment separation and detection were executed on the 3,500 Genetic Analyzer (Thermo Fisher Scientific). The results were collected on Data Collection v 3.3 and analyzed in Gene Mapper v. 5 (Thermo Fisher Scientific).

Genomic and statistical data analysis

Genomic data analysis was done following the pipeline: 1) the alignment to the reference genome (hg38) and variant caller with DRAGEN Enrichment v. 3.9.5; 2) the annotation with Annotation Engine v.3.15; 3) the consequence prediction by PolyPhen and Sift; 4) the variants were filtered in the software Variant Interpreter v.2.16.1.300

The ancestral inference analysis was done with STRUCTURE v.2.3.4 using the option for an admixture model.

Diagnostic assessment

Genomic results

After applying variant filters (pass quality and association including pathogenic, likely pathogenic, and of uncertain significance), nine variants were displayed to be involved in the diagnosis of subject A; however, two intronic and two PolyPhen-predicted benign variants were discarded. The disease-relevant variants are presented in Table 1.

TABLE 1
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Table 1. Genomic variants found in Subject A.

After applying variant filters (pass quality and association including pathogenic, likely pathogenic, and of uncertain significance) in subject B, six variants were found; however, one intronic and three predicted as benign by PolyPhen were discarded. The two diagnosis-associated variants are presented in Table 2.

TABLE 2
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Table 2. Genomic variants found in Subject B.

Both individuals presented the same mutation c.905G>A p.(Arg302Gln) in the gene PRKAG2, which has been associated with PRKAG2 cardiac syndrome.

Ancestral characterization

Subject A has a major European (51%) composition, followed by Native American (43.9%) and African (5.1%).

Moreover, subject B also has a major European (51.1%), followed by Native American (41.6%) and African (7.3%) composition.

Data corroborates that both individuals are a population mixture, in agreement with their initial self-identification.

Discussion

Nowadays, genetic testing is increasingly recommended, as it provides helpful information for clinical management, including early diagnosis, family screening, and targeted therapy for cardiovascular diseases. Although, NGS has limitations, such as the need for bioinformatic knowledge for sample processing, interpretation of variants of unknown significance, or management of incidental findings (16). The American Heart Association has encouraged research in cardiovascular genetics to further understand the molecular aspects of these diseases (17). In the present case report, the TruSight Cardio (Illumina) kit was used; the panel of this kit consists of 174 genes that have been associated with 17 different cardiovascular diseases. By analyzing this amount of information, the chances of identifying pathogenic or likely pathogenic variants associated with the clinical diagnosis increase.

Heart diseases are the most common cause of death with no correlation with demographic or ethnic factors (5, 11). Among cardiomyopathies, HCM is the most common condition (18). Sarcomeric protein mutations have been primarily associated with familial or sporadic cases of HCM; however, non-sarcomere proteins involved in biological processes such as cellular metabolism have also been correlated to HCM (19). Moreover, regarding WPW, about 2 to 5% of patients diagnosed with HCM exhibit WPW (11, 20, 21).

The serine/threonine protein kinase AMPK regulates cellular energetic homeostasis. The enzyme is stimulated by AMP concentration and the activity of the AMPK-kinase; its principal function is to counterbalance ATP depletion. Moreover, AMPK comprises three subunits (α, β, γ). The Gamma 2 regulatory subunit of AMP-Activated Protein Kinase (PRKAG2) activity enhances the Alpha subunit activation by binding to AMP (21, 22). Mutations in the gene that encodes PRKAG2 have been associated with glycogen storage cardiomyopathies by disrupting AMPK's ability to bind to AMP, dysregulating the metabolic and glucidic uptake, and causing the deposition of amylopectin and glycogen (5). The symptoms of the PRKAG2 cardiac syndrome vary, ranging from asymptomatic to a phenotype that includes cardiac hypertrophy, primarily involving the left ventricle, supraventricular tachycardia (WPW), increased risk of heart failure, and sudden cardiac death (5, 22). The results of NGS identified a pathogenic missense mutation G>A at position 905, causing a change from arginine to glutamine at codon 302, exon 7 of the PRKAG2 gene, in both subjects; however, only subject A presents WPW.

Similarly, different mutations in the gene TTN were found. In subject A, a missense mutation Arg14996Cys, and in subject B, a missense mutation Ile2686Val; however, both variants are categorized as variants of uncertain significance (VUS), and mutations in the TTN gene have been primarily associated with dilated cardiomyopathy, not hypertrophic (23, 24). Moreover, three more variants were found in subject A, two VUS in the genes APOB and PKP2, and one likely pathogenic variant in the gene GCKR; this variant has been associated with a higher risk of type 2 diabetes (25).

Ancestry analyses were performed to determine the genetic background of both subjects. Subjects A and B had mainly European ancestry components. Databases such as Allele Frequency Aggregator (26), The Exome Aggregation Consortium (ExAC) (27), and The genome Aggregation Database-Exomes (gnomAD-Exomes) (28) were used for information regarding the frequency, in Latin America, of the identified variant. The mutation has not been reported in Latin American populations; hence, this is the first report of an Arg302Gln mutation in the PRKAG2 gene in Latin America.

Conclusion

Genetic testing is a useful tool as it can provide important information regarding a disease, including its cause and consequences, not only for single individuals but also to identify at-risk relatives. Furthermore, NGS results could guide the physician into targeted therapy. In the present case report, a missense pathogenic Arg302Gln mutation in the PRKAG2 gene has been identified in two related Ecuadorian Subjects diagnosed with hypertrophic myocardiopathy and Wolff-Parkinson-White. The variant has not been reported in Latin America; hence, this is the first report of the Arg302Gln mutation in the PRKAG2 gene in mestizo Ecuadorian subjects with mainly European ancestry components.

Unfortunately, in the presented family case, the access to other family members' samples were limited due to their refusal and unavailability to participate in the study.

Data availability statement

The results are presented in the paper. Genomic Data are available in NCBI Sequence Read Archive (SRA) with the BioProject accession number PRJNA891265 (http://www.ncbi.nlm.nih.gov/bioproject/891265). For more information, please contact the corresponding author AZ (anazambrano17@hotmail.com).

Ethics statement

The studies involving human participants were reviewed and approved by Comité de Ética de Investigación en Seres Humanos—Universidad UTE. The patients/participants provided their written informed consent to participate in this study.

Author contributions

Conceptualization and formal analysis: SC-U and AZ. Resources: TS. Methodology: AZ, SC-U, PG-R, VR-P, EP-C, and RT-T. Writing—review and editing: AZ, SC-U, PG-R, VR-P, EP-C, ND, AI-R, and RT-T. Supervision, project administration, and funding acquisition: AZ. All authors contributed to the article and approved the submitted version.

Funding

The project was funded by Universidad UTE.

Acknowledgments

The authors are grateful to the patients for participating in the study and to the Cruz Roja Ecuatoriana for their collaboration.

Conflict of interest

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.

Publisher's note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fcvm.2022.1037370/full#supplementary-material

Supplementary Figure S1. Subject A electrocardiogram.

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Keywords: genomic, cardiovascular disease, case report, genetics, ancestral

Citation: Cadena-Ullauri S, Guevara-Ramirez P, Ruiz-Pozo V, Tamayo-Trujillo R, Paz-Cruz E, Sánchez Insuasty T, Doménech N, Ibarra-Rodríguez AA and Zambrano AK (2022) Case report: Genomic screening for inherited cardiac conditions in Ecuadorian mestizo relatives: Improving familial diagnose. Front. Cardiovasc. Med. 9:1037370. doi: 10.3389/fcvm.2022.1037370

Received: 05 September 2022; Accepted: 19 October 2022;
Published: 08 November 2022.

Edited by:

Neil Morgan, University of Birmingham, United Kingdom

Reviewed by:

Silvia Favilli, Meyer Children's Hospital, Italy
Emanuele Micaglio, IRCCS San Donato Polyclinic, Italy

Copyright © 2022 Cadena-Ullauri, Guevara-Ramirez, Ruiz-Pozo, Tamayo-Trujillo, Paz-Cruz, Sánchez Insuasty, Doménech, Ibarra-Rodríguez and Zambrano. 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: Ana Karina Zambrano, anazambrano17@hotmail.com

These authors have contributed equally to this work and share first authorship

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.