Good performance of the criteria of American College of Medical Genetics and Genomics/Association for Molecular Pathology in prediction of pathogenicity of genetic variants causing thoracic aortic aneurysms and dissections

Background The identification of pathogenic variant in patients with thoracic aortic aneurysms and dissections (TAAD) was previously found to be a significant indicator pointing to earlier need for surgical intervention. In order to evaluate available methods for classifying identified genetic variants we have compared the event-free survival in a cohort of TAAD patients classified as genotype-positive versus genotype-negative by the American College of Medical Genetics and Genomics and the Association for Molecular Pathology (ACMG-AMP) criteria or by ClinVar database. Methods We analyzed previously unreported cohort of 132 patients tested in the routine clinical setting for genetic variants in a custom panel of 30 genes associated with TAAD or the TruSight Cardio commercial panel of 174 genes associated with cardiac disease. The identified variants were classified using VarSome platform. Kaplan–Meier survival curves were constructed to compare the event-free survival between probands defined as ‘genotype-positive’ and ‘genotype-negative’ using different classifications in order to compare their performance. Results Out of 107 rare variants found, 12 were classified as pathogenic/likely pathogenic by ClinVar, 38 were predicted to be pathogenic/likely pathogenic by ACMG. Variant pathogenicity as assessed by ACMG criteria was a strong predictor of event free survival (event free survival at 50 years 83% vs. 50%, for genotype positive patients vs. reference, respectively, p  = 0.00096). The performance of ACMG criteria was similar to that of ClinVar (event free survival at 50 years 87% vs. 50%, for genotype positive patients vs. reference, respectively p  = 0.023) but independent from it as shown by analysing variants with no ClinVar record (event free survival at 50 years 80% vs. 50%, p  = 0.0039). Variants classified as VUS by ACMG criteria or ClinVar did not affect event-free survival. TAAD specific custom gene panel performed similar to the larger universal cardiac panel. Conclusions In our cohort of unrelated TAAD patients ACMG classification tool available at VarSome was useful in assessing pathogenicity of novel genetic variants. Gene panel containing the established genes associated with the highest risk of hereditary TAAD (ACTA1, COL3A1, FBN1, MYH11, SMAD3, TGFB2, TGFBR1, TGFBR2, MYLK) was sufficient to identify prevailing majority of variants most likely to be causative of the disease. Supplementary Information The online version contains supplementary material available at 10.1186/s12967-022-03251-8.


Background
There is a growing interest in better recognition of genetic factors leading to thoracic aortic aneurysms and dissections (TAAD) [1,2]. Diagnosis of TAAD leads to important clinical decisions. Although aortic size remains the main criterion for prophylactic surgical intervention, recent evidence indicates that aortic dissection may occur in nondilated or mildly dilated aorta, so aortic size loses its predictive ability [3][4][5]. Early diagnosis and subsequent prophylactic management prior to dissection significantly improves survival [6].
Previously, we described 51 TAAD patients studied with the use of whole exome sequencing (WES) or panel analysis (TruSight One, Illumina). We have reported a significant difference in event-free survival between 'genotype-positive' group consisting of patients with variants considered as pathogenic/likely pathogenic (P/LP) on account of either literature reports, protein disruption, de novo occurrence, segregation analysis or strong pathogenicity predictions as compared to 'genotype-negative' patients [7].
In the present work we analyzed an independent cohort of 132 patients tested in the routine clinical setting for variants in 30 genes associated with TAAD or 174 genes included in TruSight Cardio panel (Illumina). Considering the recent progress in development of free online databases collecting knowledge on human genetic variation we aimed to evaluate the performance of variant classification based on recommendations of American College of Medical Genetics and Genomics and the Association for Molecular Pathology (ACMG-AMP) [8]. The evaluation was based on a comparison of the event-free survival in patients classified as genotype-positive vs. genotype-negative by the ACMG-AMP criteria or by the expert curated information from the Clin-Var database.

Patients and consent
The study cohort was chosen from all index patients referred with the diagnosis of TAAD for clinical genetic testing from 2012 to 2019 to the Unit for Screening Studies in Inherited Cardiovascular Diseases, Institute of Cardiology and comprised 132 unrelated patients (all Caucasian). Patients with family history of aortic dissection aortic aneurysm, unexplained sudden death in firstdegree relatives, early onset of aortic disease, suspected connective tissue disorders were included primarily. In all patients a three-to-four generation pedigree was drawn and the data on the presence of TAAD, and other diseases in the family were collected. Every effort was made to review medical data on deceased subjects to confirm familial form of TAAD. For patients suspected of Marfan syndrome (MFS) and their relatives revised Ghent criteria were used [9] and a detailed questionnaire was applied to define the involvement of other systems and organs. Systemic score for each patient was calculated with web calculator http:// www. marfan. org/ resou rces/ profe ssion als/ marfa ndx. In addition, web questionnaires were used to assess systemic features of Loeys-Dietz syndrome http:// www. loeys dietz. org/. With regard to cardiovascular system, all patients had Doppler echocardiographic study and CT scan of the entire aorta. In particular, we collected the following data: age at diagnosis of thoracic aortic aneurysm (TAA), the history of acute aortic dissection (AAD) or prophylactic thoracic aorta surgery. Indications for elective surgery relied on available guidelines and evolved with time. Recognition of aortic root dilatation was based on echocardiography with calculation of Z-score for aortic root using Web calculator http:// www. marfan. org/ resou rces/ profe ssion als/ marfa ndx. Ascending aorta dimensions were normalized to body surface area. According to guidelines, patients were followed-up with serial examinations by two-dimensional echocardiography and/or CT scan of the aorta.
Aortic events were defined as either acute aortic dissection (AAD) or first elective aortic surgery. The result of genetic testing did not affect the timing of first surgery in any patients from the study cohort. Data concerning mitral valve included presence of mitral valve prolapse (MVP) and mitral regurgitation (MR) on echocardiography. Diagnosis for MVP was based upon published criteria [10]. Left ventricular noncompaction was diagnosed based on CMR study with the ratio of noncompacted to classified as VUS by ACMG criteria or ClinVar did not affect event-free survival. TAAD specific custom gene panel performed similar to the larger universal cardiac panel.

Conclusions:
In our cohort of unrelated TAAD patients ACMG classification tool available at VarSome was useful in assessing pathogenicity of novel genetic variants. Gene panel containing the established genes associated with the highest risk of hereditary TAAD (ACTA1, COL3A1, FBN1, MYH11, SMAD3, TGFB2, TGFBR1, TGFBR2, MYLK) was sufficient to identify prevailing majority of variants most likely to be causative of the disease. compacted myocardium greater than 2.3 during diastole on long-axis cine images [11]. Hypertrophic cardiomyopathy was defined as left ventricular hypertrophy in the absence of loading conditions, sufficient to account for the observed degree of hypertrophy, with a maximal left ventricular wall thickness ≥ 15 mm in one or more myocardial segments [12].
Familial disease was defined as the presence of > 1 patient with TAAD in the family. This study was approved by the Bioethics Committee in the Institute of Cardiology (Ref. No. 1407). All participants of the study gave an informed written consent including specific consent to genetic testing and permission to publish the results.

Genetic testing
Custom-designed (SeqCap, Roche) panel consisting of 30 genes related to aorthopathies and connective tissue disorders (

Variants assessment
We analysed variants located in the coding or splicing regions within genes of interest, of frequency no greater than 0.001 for autosomal dominant and X-linked inheritance pattern or 0.01 for autosomal recessive in both gnomAD genomes and gnomAD exomes databases. Pathogenicity, including VUS status, was assessed using ClinVar database classification and according to guidelines of ACMG-AMP using ACMG Classification tool (version 9.1.2) provided by Varsome platform and described in detail: https:// varso me. com/ about/ resou rces/ acmg-imple menta tion. Among other criteria, VarSome uses consensus of the following in silico pathogenicity predicting programmes with default settings: BayesDel_addAF, DANN, DEOGEN2, EIGEN, FATHMM-MKL, LIST-S2, M-CAP, MVP, MutationAssessor, Mutation-Taster, SIFT, PrimateAI while PhyloP100Way (conservation assessment) is used with cut offs -3.387, 3.858, 6.8, 7.2. The details of Varsome implementation of ACMG criteria are given at: https:// varso me. com/ about/ resou rces/ acmg-imple menta tion/.
Variation was considered novel when absent from ClinVar and HGMD database (release 2020.3), and had no other literature reference according to VarSome database. Thus identified P/LP variants and variants of unknown significance (VUS) were confirmed by Sanger sequencing.

Statistical analysis
Kaplan-Meier survival curves were constructed to compare the event-free survival between probands defined as 'genotype-positive' and 'genotype-negative' using different classification tools in order to compare their performance. Online tool available at https:// astat sa. com/ LogRa nkTest/ was used. Aortic events were defined as acute aortic dissection or first planned aortic surgery. For the purpose of constructing genotype positive and genotype negative groups variants with "conflicting interpretation of pathogenicity" status in ClinVar were classified according to prevailing interpretation and in absence of such the less categorical interpretation was chosen (e.g., likely benign over benign or VUS over likely pathogenic). Finally, 'genotype-negative' reference group was created consisting of patients with no rare variant found or with no other variant(s) then benign or likely benign (B/LB) by ClinVar classification. One patient who had a likely   3 required another surgical treatment. AAD following any planned procedure occurred in 3 patients. The remaining 50 (38.6%) patients were diagnosed with TAA at mean age of 45.5 years, however they did not meet criteria for surgical correction. Of the 50 patients with TAA, the majority (n = 43) had aortic root dilatation with mean z score of 3.9 and dilation of both root and ascending aorta was found in 20/50 patients.

Clinical findings
In 24 patients the diagnosis of MFS was made and in 15 patients with TAAD genetic examination was performed to confirm/exclude the diagnosis of MFS. In the whole group co-existing abnormalities included: bicuspid aortic valve-28 patients, coarctation of the aorta (CoA) and patent ductus arteriosus (PDA)-1 patient, MVP with MR (n = 9), left ventricular noncompaction in one female patient with bradycardia and hypertrophic cardiomyopathy in two patients. Peripheral artery aneurysms were present in 6 (4.5%), history of stroke in 8 (6.1%), and coronary artery disease in 6 (11.7%) of patients. More than half of the whole study group 73 (55.3%) had hypertension. Familial disease was found in more than one third of TAAD patients (n = 45, 34%). Of these, AAD in first degree relative was found in 19 patients (14.4%). In addition, a family history of unexplained sudden death was present in 10 (7.6%) subjects.

Variant classification by ACMG and ClinVar criteria
Overall, 107 variants in 73 (55%) patients were identified. According to both ClinVar and ACMG, no compound heterozygotes or homozygotes for any pathogenic (P), likely pathogenic (LP), or VUS variant in any of the genes associated with recessive inheritance of TAAD were found. According to ClinVar, among genes associated with autosomal dominant or X-linked inheritance pattern 12 P/LP, 25 VUS, 23 B/LB and 47 variants with no record were found. According to the ClinVar classification, 12 patients (9.1%) had at least one P/LP variant, 10 patients (7.6%) had only B/LB variant(s) and 51 (38.6%) patients had only variant(s) of unknown status (either VUS or no record). Full list of identified variants is available in Additional file 1: Table S1.
Eleven out of 12 variants classified as P/LP by ClinVar were also predicted to be P/LP by ACMG criteria and one was classified as VUS, however another variant in the same patient was classified as P/LP by ACMG alone, so a total of 12 patients had variants classified by both Clin-Var and ACMG as P/LP (in one patient classifications apply to 2 different variants). Most variants (60%) classified as VUS by ClinVar were predicted to be B/LB by ACMG; 32% were predicted as VUS and 8%-P/LP. Out of variants classified as B/LB by ClinVar alone one variant (4.3%) had conflicting (LP) prediction by ACMG. Among variants with no ClinVar record as much as 51.1% were predicted to be P/LP; 29.8% were predicted VUS and 19.1%-B/LB. Based on the ACMG classification 36 patients (27.3%) had at least one P/LP variant, 14 (10.6%)-at least one VUS with no P/LP variants and 23 (17.4%)-only B/ LB variant(s). The distribution of ACMG predictions depending on the ClinVar classification is shown in Fig. 1.

Variant pathogenicity as assessed by ACMG criteria is a strong predictor of event free survival
There was a highly significant difference in event-free survival when genotype positive group consisting of all patients with variants classified by ACMG as P/LP (including those listed in ClinVar) was compared to reference group of patients with no variant found or with variants classified as B/LB by both ClinVar and ACMG, p = 0.00096. As can be seen, at 50 years of age 50% of patients from the reference group underwent surgery compared to 83% in genotype-positive group (Fig. 2).
We noted that the observed effect was found both among patients who suffered from AAD (p = 0.02) and those who underwent prophylactic thoracic aorta surgery (p = 0.006) with no apparent difference between the two groups (p = 0.18, Additional file 1: Figure S1).

The performance of ACMG criteria in predicating event free survival is independent from ClinVar information
Since ClinVar status is included in ACMG criteria (PP5, BP6), the important question is to what extent prediction by ACMG criteria is independent from ClinVar data. In order to test this we analysed the data after dividing the ACMG positive group into those positive also according to Clinvar data (n = 12) and those positive only by ACMG but not ClinVar (n = 24). We found that the variants classified as P/LP by ACMG alone were associated with significantly shorter event-free survival compared to genotype-negative group, p = 0.0039 (Fig. 3a). At 50 years of age 80% of patients from genotype-positive group underwent surgery compared to 50% on the reference group. Furthermore, there was no significant difference in event-free survival between 12 patients with P/LP variants according to both ClinVar and ACMG compared to 24 patients carrying variants predicted to be P/LP by ACMG criteria alone, p = 0.90 (Fig. 3b).
As expected, the 12 variants classified by ClinVar as P/LP were associated with significantly shorter eventfree survival compared to the reference group (patients with no rare variant or variant(s) classified by ClinVar as benign/likely benign (B/LB), p = 0.023 (Fig. 3c). At 50 years of age 87% of patients from genotype-positive group underwent surgery. There was also no significant difference in event-free survival between variants classified as B/LB by ACMG alone and the reference group, p = 0.87 (Fig. 3d).

Variants classified as VUS by either ACMG criteria or ClinVar do not affect event-free survival
In a similar way we analysed event-free survival in patients with variants classified as VUS but we found no significant difference either between those with variants classified as VUS by ACMG alone versus reference group (p = 0.35, Fig. 4a), those with VUS by ACMG criteria alone compared to VUS by ClinVar (p = 0.18, Fig. 4b) or those with VUS by ClinVar and reference group (p = 0.65, Fig. 4c).

Discussion
ClinVar being an expert knowledge-based database enables only the classification of variants with the existing evidence regarding observed health status. Novel variants and those lacking sufficient evidence add to the growing burden of VUS. In silico algorithms [13] add valuable supporting evidence regarding pathogenicity of given variant. The development of ACMG-AMP criteria which combine both lines of evidence with many levels of supporting information into an integrated prediction was a cornerstone in unifying interpretation of clinical significance of genetic variants. Since their initial development the criteria were evaluated by multiple laboratories, several areas for improvement were identified and there is an agreement on the need of further validation [14,15]. In the present study we have tested and found good performance of an online tool available at varsome. com which allows classification based on ACMG-AMP criteria. Although the tool doesn't cover all the criteria and is the subject to constant change in the algorithms implementing the ACMG-AMP criteria, it is free and convenient to use (https:// varso me. com/ about/ resou rces/ acmg-imple menta tion/). The constantly improving functionalities of the AMG-AMP tool result in the growing number of more definitive predictions (B, LB, LP and P) and decreasing VUS classifications. Indeed, after application of ACMG-AMP criteria out of 72 variants having no ClinVar record or classified as VUS only 22 variants kept their VUS status (26 were classified as P/LP and 24 as B/LB). The goal of our study was to test the accuracy of these predictions using clinical data and ClinVar database as a reference. Similar to our previous findings [7], patients carrying known pathogenic variants (P/LP by ClinVar), had AAD or were referred for elective aortic surgery significantly earlier than patients in whom no rare variants in genes of interest or only variants classified as B/LB by ClinVar were identified. Importantly, the genotype-positive group according to the ACMG verdict alone had similar (significant) difference in the event-free survival vs. the reference group as the group defined by ClinVar alone. Furthermore, there was no significant difference in event-free survival when we compared genotype-positive group according to Clin-Var to patients carrying variants predicted to be P/LP by ACMG criteria alone. In the similar way, there was no significant difference between patients carrying only B/ LB variants according to ACMG alone vs. the reference group. These findings indicate that ACMG predictions in regard to TAAD-susceptibility genes are of similar high clinical significance to information provided by ClinVar. We also observed that among variants classified as pathogenic, those predicted to cause LOF were associated with higher severity then the remaining variants. Thus, variant type (LOF vs. non LOF) could provide additional clinically useful information. It is likely that in the future even better predictions will be possible based on knowledge collected for individual variants in sufficiently powered studies. Interestingly, in our cohort of TAAD patients there was no significant difference in disease progression between patients carrying VUS by either ACMG or ClinVar vs. the reference group suggesting that variants lacking any sort of evidence for being P/LP are more likely to be B/LB, at least regarding being the cause of monogenic disease. However, it should be noted that this does not preclude their role as risk factors in multifactorial form of disorder. Interestingly, our data are consistent with the findings from the study of 1005 patients diagnosed with nonischemic dilated cardiomyopathy which analysed prognostic impact of diseasecausing variants classified based on the ACMG-AMP criteria. The rate of major adverse cardiovascular events, end stage heart failure and malignant ventricular arrhythmia in 10-year follow-up was significantly higher in the genotype-positive group compared to the genotype-negative but showed no trend towards higher rate of these conditions among patients carrying VUS [16].
Our results also indicate that the TAAD specific panel performs similar to the larger universal cardiac panel. Out of 22 variants identified using TAAD-specific panel and predicted to be P/LP by ACMG and/or VarSome only one variant (in the HCN4 gene) wouldn't have been found if universal cardiac panel was used. This observation supports previous reports suggesting that use of smaller gene panels consisting of the most frequently mutated genes may be a cost-effective strategy as a first step of the genetic diagnosis for TAAD patients [17].
Furthermore, based on our analysis of TAAD patients, the P/LP variants we found by either ClinVar or ACMG resided mainly within the relatively few genes (FBN1, SMAD3, TGFB2, TGFBR1, COL3A1, MYH11, MYLK) generally agreed to be "definitively" associated with hereditary TAAD [2] and the highest risk of early fatal complications [18]. Patients with genetic defects in TGFBR1, TGFBR2, SMAD3, TGFB2 (affecting TGF-β signalling pathway), COL3A1 (extracellular matrix component), FBN1 (TGF-β signalling affecting extracellular matrix component), MYH11, ACTA2, MYLK and PRKG1 (structural components and modifiers of smooth muscle layer of the aorta) are at risk of dissection or rupture at aortic diameters less than 5.0 cm recommended for surgical intervention, and therefore sequencing is of key importance for decision-making regarding the time of prophylactic surgery [1].