Interstitial Lung Disease Panel

SEQmethod-seq-icon Our Sequence Analysis is based on a proprietary targeted sequencing method OS-Seq™ and offers panels targeted for genes associated with certain phenotypes. A standard way to analyze NGS data for finding the genetic cause for Mendelian disorders. Results in 21 days. DEL/DUPmethod-dup-icon Targeted Del/Dup (CNV) analysis is used to detect bigger disease causing deletions or duplications from the disease-associated genes. Results in 21 days. PLUSmethod-plus-icon Plus Analysis combines Sequence + Del/Dup (CNV) Analysis providing increased diagnostic yield in certain clinical conditions, where the underlying genetic defect may be detectable by either of the analysis methods. Results in 21 days.

Test code: PU0301

The Blueprint Genetics Interstitial Lung Disease Panel is a 24 gene test for genetic diagnostics of patients with clinical suspicion of familial idiopathic pulmonary fibrosis, other interstitial pulmonary diseases or unspecified pulmonary fibrosis.

The most common interstitial lung disease (ILD) is idiopathic pulmonary fibrosis (IPF). Autosomal dominant mutations in five genes (TERT, TERC, SFTPC, SFTPA1and SFTPA2) are attributed in up to 45% of cases with familial pulmonary fibrosis. Moreover, the panel consist substantial set of other genes associating to dominant, recessive and X-linked syndromes such as dyskeratosis congenita, Hermansky-Pudlak syndrome, surfactant metabolism disorders and tuberous sclerosis that may also present with pulmonary fibrosis.

About Interstitial Lung Disease

ILDs are a heterogeneous group of disorders that affect the lung parenchyma. ILDs are often associated with systemic diseases like vasculitis or other rheumatic diseases and thus the number of different entities is over 100. With ILD, the tissue and space between the air sacs of the lungs (the interstitium) is affected by inflammation or scarring (fibrosis). It concerns alveolar epithelium, pulmonary capillary endothelium, basement membrane, perivascular and perilymphatic tissues. The most common ILD is idiopathic pulmonary fibrosis (IPF) that has been increasingly associated with mutations in genes encoding telomerases. These mutations cause low telomerase activity, accelerated telomere shortening and disturbance in lung stem cells. Disease can cluster in families and familial pulmonary fibrosis is defined as IPF in two or more first-degree relatives (parent, sib, or offspring). Besides telomerase-associated genes, surfactant protein-associated genes are found in cases with idiopathic pulmonary fibrosis. Proportion of familial pulmonary fibrosis attributed to mutation in four genes (TERT, TERC, SFTPC and SFTPA2) is up to 45 %. ILD is also associated with hyper IgE-syndrome (STAT3) as well as tuberous sclerosis (TSC1, TSC2) Estimated incidence of ILD is 5.4/100,000.

Availability

Results in 3-4 weeks. We do not offer a maternal cell contamination (MCC) test at the moment. We offer prenatal testing only for cases where the maternal cell contamination studies (MCC) are done by a local genetic laboratory. Read more.

Genes in the Interstitial Lung Disease Panel and their clinical significance
GeneAssociated phenotypesInheritanceClinVarHGMD
ABCA3Interstitial lung disease, Surfactant metabolism dysfunction, pulmonaryAD/AR11181
CSF2RA*Surfactant metabolism dysfunction, pulmonaryXL214
DKC1Hoyeraal-Hreidarsson syndrome, Dyskeratosis congenitaXL4569
ELMOD2Familial idiopathic pulmonary fibrosisAD/AR
HPS1*Hermansky-Pudlak syndromeAR2641
HPS4Hermansky-Pudlak syndromeAR1415
ITGA3Interstitial lung disease with nephrotic syndrome and epidermolysis bullosaAR611
NF1*Watson syndrome, Neurofibromatosis, Neurofibromatosis-Noonan syndromeAD2612607
NKX2-1Thyroid cancer, nonmedullary, Choreoathetosis, hypothyroidism, and neonatal respiratory distressAD13123
PARN*Pulmonary fibrosis and/or bone marrow failure, Dyskeratosis congenitaAD/AR1119
RTEL1Pulmonary fibrosis and/or bone marrow failure, Dyskeratosis congenitaAD/AR2726
SFTPA1Idiopathic pulmonary fibrosisAD5
SFTPA2Pulmonary fibrosis, idiopathicAD28
SFTPBSurfactant metabolism dysfunction, pulmonaryAR530
SFTPCSurfactant metabolism dysfunction, pulmonaryAD781
SLC7A7Lysinuric protein intoleranceAR5165
SLC34A2Pulmonary alveolar microlithiasisAR518
SMPD1Niemann-Pick diseaseAR52230
STAT3Hyper-IgE recurrent infection syndrome, Autoimmune disease, multisystem, infantile onsetAD27133
TERCAplastic anemia, Pulmonary fibrosis and/or bone marrow failure, telomere-related, Dyskeratosis congenitaAD3660
TERTAplastic anemia, Pulmonary fibrosis and/or bone marrow failure, telomere-related, Dyskeratosis congenitaAD/AR39133
TINF2Revesz syndrome, Dyskeratosis congenitaAD2033
TSC1Lymphangioleiomyomatosis, Tuberous sclerosisAD61306
TSC2Lymphangioleiomyomatosis, Tuberous sclerosisAD141977
  • * Some regions of the gene are duplicated in the genome leading to limited sensitivity within the regions. Thus, low-quality variants are filtered out from the duplicated regions and only high-quality variants confirmed by other methods are reported out. Read more.

Gene, refers to HGNC approved gene symbol; Inheritance to inheritance patterns such as autosomal dominant (AD), autosomal recessive (AR) and X-linked (XL); ClinVar, refers to a number of variants in the gene classified as pathogenic or likely pathogenic in ClinVar (http://www.ncbi.nlm.nih.gov/clinvar/); HGMD, refers to a number of variants with possible disease association in the gene listed in Human Gene Mutation Database (HGMD, http://www.hgmd.cf.ac.uk/ac/). The list of associated (gene specific) phenotypes are generated from CDG (http://research.nhgri.nih.gov/CGD/) or Orphanet (http://www.orpha.net/) databases.

GeneGenomic location HG19HGVSRefSeqRS-numberCommentReference
TSC2Chr16:2098067c.-30+1G>CNM_000548.3rs587778004
NF1Chr17:29657848c.5812+332A>GNM_001042492.2rs863224491
DKC1ChrX:153991099c.-142C>GNM_001363.3rs199422241
NF1Chr17:29577934c.4110+1802delANM_001042492.2rs863224944

Blueprint Genetics offers a comprehensive Interstitial Lung Disease Panel that covers classical genes associated with familial idiopathic pulmonary fibrosis, other interstitial pulmonary diseases, pulmonary eosinophilia (not elsewhere classified) and unspecified pulmonary fibrosis. The genes are carefully selected based on the existing scientific evidence, our experience and most current mutation databases. Candidate genes are excluded from this first-line diagnostic test. The test does not recognise balanced translocations or complex inversions, and it may not detect low-level mosaicism. The test should not be used for analysis of sequence repeats or for diagnosis of disorders caused by mutations in the mitochondrial DNA.

Analytical validation is a continuous process at Blueprint Genetics. Our mission is to improve the quality of the sequencing process and each modification is followed by our standardized validation process. Average sensitivity and specificity in Blueprint NGS Panels is 99.3% and 99.9% for detecting SNPs. Sensitivity to for indels vary depending on the size of the alteration: 1-10bps (96.0%), 11-20 bps (88.4%) and 21-30 bps (66.7%). The longest detected indel was 46 bps by sequence analysis. Detection limit for Del/Dup (CNV) analysis varies through the genome depending on exon size, sequencing coverage and sequence content. The sensitivity is 71.5% for single exon deletions and duplications and 99% for three exons’ deletions and duplications. We have validated the assays for different starting materials including EDTA-blood, isolated DNA (no FFPE) and saliva that all provide high-quality results. The diagnostic yield varies substantially depending on the used assay, referring healthcare professional, hospital and country. Blueprint Genetics’ Plus Analysis (Seq+Del/Dup) maximizes the chance to find molecular genetic diagnosis for your patient although Sequence Analysis or Del/Dup Analysis may be cost-effective first line test if your patient’s phenotype is suggestive for a specific mutation profile.

The sequencing data generated in our laboratory is analyzed with our proprietary data analysis and annotation pipeline, integrating state-of-the art algorithms and industry-standard software solutions. Incorporation of rigorous quality control steps throughout the workflow of the pipeline ensures the consistency, validity and accuracy of results. The highest relevance in the reported variants is achieved through elimination of false positive findings based on variability data for thousands of publicly available human reference sequences and validation against our in-house curated mutation database as well as the most current and relevant human mutation databases. Reference databases currently used are the 1000 Genomes Project (http://www.1000genomes.org), the NHLBI GO Exome Sequencing Project (ESP; http://evs.gs.washington.edu/EVS), the Exome Aggregation Consortium (ExAC; http://exac.broadinstitute.org), ClinVar database of genotype-phenotype associations (http://www.ncbi.nlm.nih.gov/clinvar) and the Human Gene Mutation Database (http://www.hgmd.cf.ac.uk). The consequence of variants in coding and splice regions are estimated using the following in silico variant prediction tools: SIFT (http://sift.jcvi.org), Polyphen (http://genetics.bwh.harvard.edu/pph2/), and Mutation Taster (http://www.mutationtaster.org).

Through our online ordering and statement reporting system, Nucleus, the customer can access specific details of the analysis of the patient. This includes coverage and quality specifications and other relevant information on the analysis. This represents our mission to build fully transparent diagnostics where the customer gains easy access to crucial details of the analysis process.

In addition to our cutting-edge patented sequencing technology and proprietary bioinformatics pipeline, we also provide the customers with the best-informed clinical report on the market. Clinical interpretation requires fundamental clinical and genetic understanding. At Blueprint Genetics our geneticists and clinicians, who together evaluate the results from the sequence analysis pipeline in the context of phenotype information provided in the requisition form, prepare the clinical statement. Our goal is to provide clinically meaningful statements that are understandable for all medical professionals, even without training in genetics.

Variants reported in the statement are always classified using the Blueprint Genetics Variant Classification Scheme modified from the ACMG guidelines (Richards et al. 2015), which has been developed by evaluating existing literature, databases and with thousands of clinical cases analyzed in our laboratory. Variant classification forms the corner stone of clinical interpretation and following patient management decisions. Our statement also includes allele frequencies in reference populations and in silico predictions. We also provide PubMed IDs to the articles or submission numbers to public databases that have been used in the interpretation of the detected variants. In our conclusion, we summarize all the existing information and provide our rationale for the classification of the variant.

A final component of the analysis is the Sanger confirmation of the variants classified as likely pathogenic or pathogenic. This does not only bring confidence to the results obtained by our NGS solution but establishes the mutation specific test for family members. Sanger sequencing is also used occasionally with other variants reported in the statement. In the case of variant of uncertain significance (VUS) we do not recommend risk stratification based on the genetic finding. Furthermore, in the case VUS we do not recommend use of genetic information in patient management or genetic counseling. For some cases Blueprint Genetics offers a special free of charge service to investigate the role of identified VUS.

We constantly follow genetic literature adapting new relevant information and findings to our diagnostics. Relevant novel discoveries can be rapidly translated and adopted into our diagnostics without delay. These processes ensure that our diagnostic panels and clinical statements remain the most up-to-date on the market.

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ICD & CPT codes

CPT codes

SEQ81479


ICD codes

Commonly used ICD-10 codes when ordering the Interstitial Lung Disease Panel

ICD-10Disease
J84.10Familial idiopathic pulmonary fibrosis
J84.10Unspecified pulmonary fibrosis
J84Other interstitial pulmonary diseases

Accepted sample types

  • EDTA blood, min. 1 ml
  • Purified DNA, min. 5μg
  • Saliva (Oragene DNA OG-500 kit)

Label the sample tube with your patient’s name, date of birth and the date of sample collection.

Note that we do not accept DNA samples isolated from formalin-fixed paraffin-embedded (FFPE) tissue.

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