Cardiological Disease Genetic Panels

Genetic factors play a role in some heart and vascular diseases. The CardioNext® and CardioScreen® tests investigate genetic changes associated with cardiovascular predisposition or inherited heart diseases. When evaluated together with the person's clinical findings and family history, the results can contribute to diagnosis, follow-up and risk assessment of family members.

 

Who is it suitable for?

  1. With the evaluation of a cardiology and/or medical genetics specialist, genetic testing may be considered in the following people:
  2. People diagnosed with, or suspected of having, an inherited heart muscle disease (cardiomyopathy).
  3. People suspected of having inherited rhythm disorders such as long QT or Brugada syndrome.
  4. People with a family history of unexplained sudden death at a young age, heart muscle disease or an inherited rhythm disorder.
  5. People in whose family a genetic change causing heart disease has been identified.
  6. Patients in whom an inherited cause is suspected after an unexplained cardiac arrest.

The appropriate test is selected according to the person's symptoms and family history. The detection of a genetic predisposition does not necessarily mean that the disease will develop; a negative result does not completely rule out the risk of heart disease.

 

Our genetic tests

CardioNext® — Cardiovascular Genetic Predisposition Panel
Examines selected genetic variants involved in processes related to heart and vascular health, such as lipid metabolism, blood pressure and coagulation. The findings are evaluated together with cholesterol, blood pressure, lifestyle and family history. These polymorphisms alone do not predict cardiovascular risk; risk is assessed with cholesterol, blood pressure, smoking and diabetes.

CardioScreen® — Cardiomyopathy Panel
Investigates genes associated with inherited diseases that affect the structure and function of the heart muscle. It can help identify the genetic cause of heart muscle disease and evaluate family members.

CardioScreen® — Inherited Heart Diseases Associated with Sudden Cardiac Arrest Panel
Examines genes associated with inherited rhythm disorders and heart muscle diseases that can lead to sudden cardiac arrest. In suitable patients, it can support the planning of personalized follow-up and preventive measures.

 

During working hours, you can quickly apply with a simple blood test by visiting our Nicosia or Kyrenia laboratory branches.

Cardiology Genetic Test Panels

CardioNext® 50 SNPs(Single nucleotide polymorphisms) NGS screening for cardiovascular diseases (54 genes)

  • ACT (-51 G-T), APOA1 (-75 G>A ), APOB (R3500Q), APOC3 (T3175G), APOC3 (T3206G), APOE (E2, E3, E4), CETP (G279A), CETP (G1533A), GJA4 (CX37) (Pro319Ser), HMGCR (-911 C-A), LPL (C1595G), MMP3 (1171 5A/6A), NOS3 (-786 T>C), NOS3 (Glu298Asp), NOS3 (VNTR intron 4), PON1 (Gln192Arg), SREBF2 (Gly595Ala), F2/prothrombin (G20210A), F5 (Leiden), F5 (Y1702C), F5 (H1299R), F5 (R306T/Cambridge), F13A1 (V34L), FGB/Beta Fibrinogen (-455G-A), ITGB3/HPA (Leu33Pro), PAI-1 (1 bp Del/Ins 4G/5G), ACE (I/D), AGT (M235T), ADRA2B (Ins>Del Codon 299), ADRB1 (Gly389Arg), ADRB2 (Gly16Arg), ADRB2 (Gln27Glu), ADRB3 (Trp64Arg), NPY (Leu7Pro), CBS (C699T), CBS (T1080C), MTHFR (C677T), MTHFR (A1298C), MTR (A2756G), MTRR (A66G), IL-1B (-511 C-T), IL-6 (G634C), IL-6 (G-174C), IL-10 (-1082 G-A), IFN- (+874 T-A), TNF (-308 G-A), VEGF (-2578 C-A), MnSOD (C -28 T), MnSOD (T175C), SOD3 (C760G)

    CardioScreen® CardiomyopathyNGS screening (46 genes)

    • ABCC9, ACTC1, ACTN2, ANKRD1, CASQ2, CAV3, CRYAB, CSRP3, CTF1, DES, DSC2, DSG2, DSP, DTNA, EMD, FHL2, GLA, JUP, LAMA4, LAMP2, LDB3, LMNA, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYLK2, MYOZ2, NEXN, PKP2, PLN, PRKAG2, RBM20, RYR2, SGCD, TAZ, TCAP, TMEM43, TNNC1, TNNI3, TNNT2, TPM1, TTN, TTR, VCL

      CardioScreen® Prevention of Sudden Cardiac ArrestNGS screening (166 genes)

      • ABCC9, ABCG5, ABCG8, ACTA1, ACTA2, ACTC1, ACTN2, AKAP9, ALMS1, ANK2, ANKRD1, APOA5, APOB, APOC2, APOE, BAG3, BRAF, CACNA1C, CACNB2, CALM1, CALR3, CASQ2, CAV3, CBL, CBS, CETP, COL3A1, COL5A1, COL5A2, COX15, CRELD1, CRYAB, CSRP3, CTF1, DES, DMD, DNAJC19, DOLK, DPP6, DSC2, DSG2, DSP, DTNA, EFEMP2, ELN, EMD, EYA4, FBN1, FBN2, FHL1, FHL2, FKRP, FKTN, FXN, GAA, GATAD1, GCKR, GJA5, GLA, GNAS, GPD1L, GPIHBP1, HADHA, HCN4, HFE, HRAS, HSPB8, JAG1, JPH2, JUP, KCNA5, KCND3, KCNE1, KCNE2, KCNE3, KCNH2, KCNJ2, KCNJ5, KCNQ1, KRAS, LAMA2, LAMA4, LAMP2, LDB3, LDLR, LDLRAP1, LMF1, LMNA, LPL, LTBP2, MAP2K1, MAP2K2, MYBPC3, MYH11, MYH6, MYH7, MYL2, MYL3, MYLK, MYLK2, MYO6, MYOZ2, MYPN, NEXN, NKX2-5, NODAL, NOTCH1, NPPA, NRAS, PCSK9, PKP2, PLN, PRKAG2, PRKAR1A, PTPN11, RAF1, RBM20, RYR1, RYR2, SALL4, SCN1B, SCN2B, SCN3B, SCN4B, SCN5A, SCO2, SDHA, SEPN1, SGCB, SGCD, SGCG, SHOC2, SLC25A4, SLC2A10, SMAD3, SMAD4, SNTA1, SOS1, TAZ, TBX20, TBX3, TBX5, TCAP, TGFB2, TGFB3, TGFBR1, TGFBR2, TMEM43, TMPO, TNNC1, TNNI3, TNNT2, TPM1, TRDN, TRPM4, TTN, TTR, VCL, ZIC3