Hereditary recurrent fevers (HRFs) are a group of monogenic autoinflammatory diseases characterised by recurrent bouts of fever and serosal inflammation that are caused by pathogenic variants in genes important for the regulation of innate immunity. Discovery of the molecular defects responsible for these diseases has initiated genetic diagnostics in many countries around the world, including the Middle East, Europe, USA, Japan and Australia. However, diverse testing methods and reporting practices are employed and there is a clear need for consensus guidelines for HRF genetic testing.
Draft guidelines were prepared based on current practice deduced from previous HRF external quality assurance schemes and data from the literature. The draft document was disseminated through the European Molecular Genetics Quality Network for broader consultation and amendment. A workshop was held in Bruges (Belgium) on 18 and 19 September 2011 to ratify the draft and obtain a final consensus document. An agreed set of best practice guidelines was proposed for genetic diagnostic testing of HRFs, for reporting the genetic results and for defining their clinical significance.
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Patients with hereditary recurrent fevers (HRFs) present with recurrent bouts of fever and inflammatory symptoms involving, in particular, the abdomen, joints and skin.1 ,2 The causative genes for HRFs encode proteins involved in the regulation of innate immunity, mainly by affecting proinflammatory cytokines and apoptosis pathways. While familial Mediterranean fever (FMF) is relatively common in several Mediterranean and Middle Eastern populations,3 most HRFs are rare diseases. The best-characterised HRFs are two recessively inherited diseases: (FMF, gene MEFV, MIM 608107) and mevalonate kinase deficiency (MKD, gene MVK, MIM 251170) and two dominantly inherited diseases: tumour necrosis factor (TNF) receptor-associated periodic syndrome (TRAPS, gene TNFRSF1A, MIM 191190) and cryopyrin-associated periodic syndrome (CAPS, gene NLRP3, MIM 606416). Patients with HRF often display similar inflammatory symptoms with variable intensity and localisation of symptoms, making their clinical diagnosis difficult.
Since the discovery of these four HRF genes, almost 700 nucleotide variants have been identified and recorded in Infevers, a database dedicated to autoinflammatory sequence variants (http://fmf.igh.cnrs.fr/ISSAID/infevers/).4,–,6 Some of these variants are clearly pathogenic, but most are unconfirmed or seemingly non-pathogenic variants. A significant number of patients clinically diagnosed with recessive HRFs have been found to carry only one disease-associated mutation in the respective genes7 despite extensive searching for a second pathogenic mutation in the coding region,8 ,9 and continuing search for mutations affecting regulatory sequences or transcript splicing that would affect gene expression.10 ,11
Genetic testing for HRF is a logical and feasible way to corroborate clinical diagnosis.12 ,13 Five-year experience of external quality assessment and proficiency testing (PT) (external quality assurance/PT) conducted between 2006 and 2010 showed that although there has been an impressive improvement in the quality of HRF testing and reporting, many issues still remain to be addressed and standardised.14 Guidelines using the standard definition by Field and Lohr15 are now proposed to provide a framework for best laboratory practice and reporting on the genetic diagnosis of HRFs as agreed by an international consortium of experts in the field. They are intended to be used primarily by molecular geneticists and by other health professionals involved in the care of these patients.
A draft report was written by the organisers and assessors of the European Molecular Genetics Quality Network for HRFs with reference to relevant literature, reviews of reports issued during the five previous international HRF meetings, web-based resources relating to the subject and examples of guidelines for other hereditary diseases (eg, haemochromatosis,16 cystic fibrosis17 and von Willebrand18 diseases). The draft was disseminated to molecular geneticists and clinicians working in the field of HRFs and discussed with them during a best practice workshop held in Bruges (Belgium) on 18 and 19 September 2011. In the light of feedback of the participants, amendments were made and a second draft was disseminated by email, after which, the final document was ratified.
Indications for HRF testing
Minimal requirements for the genetic test
We suggest that the following minimum set of requirements should be obtained: patient name, date of birth, gender, ethnicity/origin, written informed consent (depending on country-specific law), referring doctor's name and contact details of the person who will receive the results.
The main indication for genetic testing of HRFs is in the case of a patient with a clinical symptom pattern consistent with one or more of the syndromes. Thus, clinical data that justify the choice of one or more HRFs genetic tests are required. It is not unusual that when overlapping, partial or atypical clinical symptoms impede an accurate clinical diagnosis, screening of several HRF-responsible genes gives the correct diagnosis.
The clinical HRF referral usually includes the frequency of attacks, duration, sites affected, acute phase reactants levels, biomarkers for mevalonic aciduria or amyloidosis and a letter by an expert clinician. An example of a clinical chart is provided in online supplementary figure S1. It has been established in France by GenMAI, the national network for genetic diagnosis of autoinflammatory diseases, in conjunction with the clinical reference centres. Decision trees for genetic diagnosis in atypical patients and patients with sporadic disease have been proposed.13 ,19 In addition, a diagnostic score for children with periodic fever has been elaborated in Italy.20
Presymptomatic diagnosis and carrier status
In general, presymptomatic diagnosis is not advisable, as its interpretation is inconclusive, may be complicated for mutations with incomplete penetrance and it usually does not call for medical intervention. Presymptomatic testing may be recommended after genetic counselling for asymptomatic family members when a severe genotype has been found in relatives with an overt disease, or if there is a family history of amyloidosis. Follow-up of people at risk may avoid occurrence of this life-threatening complication. However, whether such cases should be given prophylactic treatment remains controversial. Evaluation of carrier status could be recommended in healthy relatives to phase two known disease-associated or new mutations, when identified in an affected patient.
Prenatal diagnosis and preimplantation genetic diagnosis
Generally prenatal diagnosis (PND) and preimplantation genetic diagnosis (PGD) are not considered appropriate for HRF as most of these conditions are treatable and symptoms usually decrease over time. However, it may be appropriate to discuss PND or PGD in families affected by a particularly severe form of MKD or chronic infantile neurological, cutaneous and articular syndrome (CINCA) as these disorders can be associated with debilitating complications: blindness, deafness, mental retardation, ataxia and bone deformation. However, most severe CINCA-associated mutations occur de novo and this should be considered before offering PND and PGD. If PND is planned, it should be performed after genetic counselling.
Diagnostic laboratories and expert structures
Genetic diagnosis for HRFs is now widely available. There are 99 laboratories providing FMF testing in Europe (source Orphanet at www.orpha.net).21 A registry of sequence variants was developed online at http://fmf.igh.cnrs.fr/ISSAID/infevers to assist the molecular geneticist. It provides a comprehensive and updated list of gene variants and a reference database for the mutation nomenclature, but an accurate phenotype–genotype correlation is not available. In addition, clinical reference centres were formally nominated or are recognised in several countries (France, Italy, Spain, UK, Germany, Turkey, Israel, USA…). As HRFs are rare diseases mostly caused by single-nucleotide substitutions, genetic testing should be referred to specialised laboratories to ensure that pertinent tests are performed and proper information is reported to clinicians, particularly those inexperienced with HRFs. These laboratories should work within a comprehensive quality management system (accreditation), use validated methods, participate annually in interlaboratory comparisons such as external quality assessment and proficiency testing for HRF and/or the relevant techniques (eg, DNA sequencing) and define a typical turn-around time.
Most laboratories focus the molecular analysis on mutational hot-spot regions in various genes. Recommendations on the reference sequence to be used for analysis and for the extent of the initial mutation screening are provided in table 1. The minimum diagnostic screen should include variants that are clearly shown to be pathogenic and that are frequently identified in patients. Although this screening recommendation is valid worldwide, the ethnic background of the patient needs to be considered. For instance, the four clearly pathogenic MEFV variants are almost exclusively found in Mediterranean populations, while the frequency of the debated p.Glu148Gln (NM_000243.2:c.442G→C) variant is as high as 20% in Asiatic countries.22 The p.Phe479Leu (NM_000243.2:c. 1437C→G) is especially relevant in Greek and Iranian patients.22 The p.Pro75Leu (NM_001065.3:c.224C→T) (usual name P46L) of TNFRSF1A is commonly found in Arabic and African populations.23 Accordingly, many laboratories have adopted a two-step strategy—that is, an initial search for the most common pathogenic variants followed, if necessary, by an extended search spanning the complete coding sequence of the various genes. For the MEFV gene, there is limited utility in searching for rare variants for patients with clinically established FMF and no mutations in exons 2, 3, 5 and 10.
A variety of techniques are used to identify HRFs gene sequence variations but direct mutation analysis by DNA sequencing is the method employed by most laboratories. Other methods include PCR with restriction enzyme digest, allele-specific PCR, PCR-single-strand conformation polymorphism and primer extension and reverse hybridisation-based kits. Commercially available kits should specify whether they are CE-IVD (in vitro diagnostics) marked or Food and Drug Administration approved. General guidelines18 should be followed. No standard primer set is recommended for amplification of the essential regions in HRF genes, but:
Primer sequences should be regularly checked for underlying single-nucleotide polymorphisms (SNPs) particularly for highly polymorphic exons of the HRF genes (eg, MEFV exons 2 or 5).
PCR primer design should avoid possible amplification of sequences from homologous genes (eg, NLRP genes).
Classification and validation of HRF sequence variants
The Human Genome Variation Society (HGVS) has recommended avoiding the use of ‘mutation’ and polymorphism' as terms with opposite meanings (pathogenic vs non-pathogenic), since functional studies are scarce or unavailable for most of the sequence variants to evaluate their pathogenicity. HRF sequence variants are associated with a broad range of phenotypes, but only a small proportion of them have been clearly shown to be the direct cause of the disease. The most common variants seen in the HRF genes are non-synonymous nucleotide changes and with the exception of MKD, no large structural mutations (deletions, duplications, rearrangement) have been reported.24 ,25 This is probably because such deleterious pathogenic variants would not be tolerated in genes that regulate host defence pathways.
We have established a classification of gene variants based on the expertise of HRF diagnostic laboratories and on the review of current publications (table 1). Interpretation should differentiate the following:
Clearly pathogenic variants. Genetic confirmation of HRFs is more straightforward in cases of sequence variants that associate with a well-recognised HRF phenotype (eg, p.Met694Val, NM_000243.2:c.2080A→G in MEFV), or those clearly altering the protein structure (eg, cysteine mutations in TNFRSF1A; deletions, insertions in MVK).When evidence is sufficient, laboratories should clearly indicate when a detected variant (or combination of variants) is predicted to cause HRFs. If the variant has been associated with severe or moderate symptoms, references could be provided but with the note that this does not necessarily predict the individual's disease phenotype.
Variants of uncertain significance. These include debated frequent variants and rare or private variants.
Variants that have been initially published as pathogenic but later reassigned. It is not unusual that some variants that have been initially described as disease-associated are now found to be common in the general population, or do not segregate with the phenotype in multiplex families, or do not have much effect on the normal function of the protein. Well-known examples are p.Glu148Gln (NM_000243.2:c.442G→C) of MEFV, p.Arg121Gln (NM_001065.3:c.362G→A) or p.Pro75Leu (NM_001065.3:c.224C→T) (usual names R92Q and P46L, respectively) of TNFRSF1A and p.Val198Met (NM_001243133.1:c.592G→A), of NLRP3 (also known as V200M).
Variants with no reliable information or new variants. Testing unaffected parental samples for the presence of a new variant is fairly straightforward and a very informative way to assess their contribution to HRF. The frequency of rare variants in ethnically matched populations could be evaluated in silico by searching various databases such as dbSNP (http://www.ncbi.nlm.nih.gov/projects/SNP/), 1000 Genomes Pilot project and PubMed. There are also other web-based tools for evaluating the degree of evolutionary conservation (eg, Genomics Evolutionary Rate Profiling: GERP, http://mendel.stanford.edu/sidowlab/downloads/gerp/index.html) and the functional impact on the protein (eg, PolyPhen-2 http://genetics.bwh.harvard.edu/pph2/). For variants that are suspected to affect transcript splicing the patient's cDNA should be analysed if available.
Variants that are clearly not the genetic cause should not be reported. Coding region SNPs frequent in the general population are often encountered. Examples are p.Arg202Gln (NM_000243.2: c.605G→A, minor allele frequency (MAF)=0.18) of MEFV which is in linkage disequilibrium with p.Met694Val, NM_000243.2:c.2080A→G,26 p.Ser52Asn (NM_000431.1:c.155G→A, MAF=0.09) of MVK and p.Gln703Lys (NM_001243133.1:c.2107C>→A, MAF=0.02) of NLRP3.27 We believe that reporting these SNPs in the context of genetic diagnosis of HRF might mislead the report recipient.
Genetic confirmation of the clinical diagnosis
As for any Mendelian conditions, the definitive genetic diagnosis of HRFs is based on the finding of unambiguous mutations in the causative genes. Theoretically, identification of one single pathogenic variant in dominant diseases, homozygosity or compound heterozygosity (confirmed by studying the parental alleles) in recessive disorders, should be enough to confirm the diagnosis. Of note, finding a single MEFV pathogenic variant in patients of Mediterranean origin does not exclude the possibility of disease-causing mutations in other HRF genes.28 However, interpretation of a result should always take into account the sensitivity of the molecular screening strategy. Failure to identify a causal mutation in a given gene can almost never exclude the diagnosis. Indeed, the entire gene is not sequenced in most routine settings and even complete gene sequencing based on PCR technology could miss a pathogenic variant (primer variants, inversion of exons, duplication of exons…) Likewise mosaicism will be most likely missed by standard sequencing.
We recommend that genetic test results should be sent to the doctor(s) designated by the patient and not directly to the patient. The referring doctor should be invited to contact the laboratory if they have not fully understood the clinical significance of the test result. In the case of family studies, genetic results should not be communicated to other relatives without their consent. We recommend that a patient's information on genetic testing results should be given by a doctor skilled in the field of HRFs or by an expert geneticist, if available.
We strongly suggest that the reports include all items recommended by the OECD quality assurance in genetic testing (http://www.oecd.org/dataoecd/43/6/38839788.pdf) and match the international standard ISO-15189. The laboratory report should be limited to a single page, with the genetic results and interpretation highlighted and the rest in smaller characters or presented in footnotes. A model report is proposed (figure 1).
Variants should be described at both the protein and nucleotide level and should comply with the latest version of HGVS nomenclature (http://www.hgvs.org/mutnomen/). It is preferable to use the three-letter amino acid code.
Wherever the sequence variant name has changed owing to renumbering of the start codon, both the standard and HGVS nomenclature should be reported, to allow the referring clinician access to the relevant literature. Examples are p.Arg121Gln (NM_001065.3:c.362G→A) (common name R92Q) of TNFRSF1A and p.Val198Met (NM_001243133.1:c.592G→A) (also known as V200M) of NLRP3.
The number for the reference sequence used should be provided.
A brief description of the testing technique and its clinical and analytical sensitivities for the specific population being screened (ie, extent of mutation screening and coverage of disease-associated mutations, region and limits of detection) should be provided.
Typical cases together with suggested clinical interpretation are listed in table 2. Reports should state, at a minimum, if the genotype is consistent or not with a diagnosis of HRF. Where the diagnosis is not confirmed genetically, the report should not state that a diagnosis of HRF is excluded. In this situation diagnosis relies on clinical judgement or criteria.
Additional comments in the report may refer to the presumed effect of the sequence variant on protein function and suggest further genetic testing or clinical management. Comments related to genotype–phenotype correlations are appropriate if there is enough evidence in the literature to support them. They are critical when discussing the risk of amyloidosis in patients with FMF with mutations affecting codons 680 or 694 of the MEFV gene, in patients with TRAPS with cysteine pathogenic variants and in familial cases of HRF with a history of amyloidosis. A comment on mild disease outcome can be considered for genotypes with mild or low penetrance sequence variants.
It is preferable to recommend referral to genetic counselling and/or to a clinical reference centre rather than to comment directly on treatment options or the predicted risk for the offspring or other family members. The clinical reference centres are better placed to fully discuss these pertinent issues. Testing should be offered to other symptomatic family members and to the parents where this can help with interpretation of the proband's results.
The other important items suggested by the OECD are summarised below:
• More than one identifier that unequivocally links the report to the patient (name, date of birth, internal reference laboratory number).
• The name of the referring healthcare professional and contact information.
• The indication for testing and specific medical information where it is relevant.
• The date of receipt of the sample and of report issuing.
• The laboratory contact information and the identity of the individual approving the report.
A consensus set of best practice guidelines has been developed for molecular genetic testing of HRFs based on feedback received from experts in this field. The guidelines described here are aimed at improving the quality of HRF molecular diagnostics and promoting harmonisation and standardisation of laboratory test reports. Understanding the molecular pathology of these diseases, their heterogeneity and genotype–phenotype correlations is steadily evolving as more data become available from large population cohorts of patients and healthy controls. A particular challenge for the genetic diagnosis of HRF will be in the interpretation of clinical relevance of variants that are found at low, but >1%, frequency in various populations. These may function as susceptibility alleles to inflammation rather than disease-associated mutations and as such may give rise to an inflammatory phenotype when inherited through digenic inheritance (in the form of double heterozygous). In that context we feel that these guidelines may need to be regularly updated.
Infevers: Registry of autoinflammatory mutations: http://fmf.igh.cnrs.fr/ISSAID/infevers/
ISSAID: Website of the International Society of Systemic Autoinflammatory Diseases: http://fmf.igh.cnrs.fr/ISSAID/
Eurofever: Registry of autoinflammatory patients: http://www.printo.it/eurofever/
Orphanet: Reference portal for information on rare diseases and orphan drugs: http://www.orpha.net/
HGVS: Reference for the nomenclature for the description of sequence variants: http://www.hgvs.org/mutnomen/
EMQN: European Molecular Genetics Quality Network: http://www.emqn.org/emqn/
This study was supported and performed within the framework of the EU projects EuroGentest (FP6-512148), Eurotraps (coordination theme 1 (health) of the European Community's FP7, grant agreement number HEALTH-F2-2008-200923 and la Région Languedoc-Roussillon) and Eurofever (EAHC, Project No2007332). It was also supported by the French Ministry of Health. The authors are indebted to Drs Catherine Dodé, Laurence Cuisset and Isabelle Jéru from the GenMAI network for the elaboration of the clinical questionnaire for the genetic diagnosis of HRFs. The authors thank Dr Robert Elles for reviewing the paper and Outi Kamarainen and Simon Patton for overseeing the HRF EQA scheme of EMQN and for the logistic support of the meeting.
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Collaborators Hatem El Shanti, Marianne Jakobsen, Kostas Kostantopoulos, Davide Martorana, Maria Grazia Pomponi, Alison Bybee, Catherine Rydlewski
Note added in proof While this manuscript was in press, a new article by Verma et al demonstrated a possible functional role of pQ703K (Q705K) in the regulation of inflammation.This variant should therefore be considered a VUS (should be in normal letters in table 1). The Q705K Polymorphism in NLRP3 Is a Gain-of-Function Alteration Leading to Excessive Interleukin-1β and IL-18 Production. Verma D, Särndahl E, Andersson H, et al.PLoS One. 2012;7:e34977. Epub 2012 Apr 17.
Provenance and peer review Not commissioned; externally peer reviewed.
Correction notice This article has been corrected since it was published Online First.
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