2023

LIPID inCode®, tests patients to identify familial hypercholesterolemia and prevent cardiovascular disease

Oxford, UK - GENinCode Plc (AIM: GENI), the genetics company focused on the prevention of cardiovascular disease and ovarian cancer, announces its collaboration with The Family Heart Foundation®, UT  Southwestern,  and other partner members to use the LIPID inCode® monogenic and polygenic test in US Primary and Secondary Care settings for the diagnosis of familial hypercholesterolemia (“FH”) with further information available to physicians for polygenic hypercholesterolemia (high levels of cholesterol) and coronary heart disease risk.

Supported by a US Department of Defense grant, the DISCOVER FH¹ mission is to “Research to improve early diagnosis of familial hypercholesterolemia (FH) through family screening and the implementation of diagnostic tools, including in the pediatric population.” LIPID inCode® is the diagnostic tool used for identification of patients with FH and cascade screening. Cascade screening is the process of screening family members once a person is diagnosed with FH in order to identify others who may be affected. This approach can identify both adults and children early in life, allowing earlier treatment with cholesterol-lowering therapies and reductions in the risk of heart disease.

Individuals tested in the program will be identified from two US healthcare systems, UT Southwestern Medical Center and the Veteran Affairs (VA) North Texas Health Care system. After an individual is genetically confirmed to have FH, the Family Heart Foundation will directly contact at-risk family members to educate them about their risk for FH, the significance, and coordinate genetic testing.  

“Collaborating with GENinCode and partners to implement FH testing brings us one step closer to broader and more accessible cascade screening at a national level, helping to save future generations from cardiovascular disease,” said Katherine Wilemon, Founder and CEO of Family Heart Foundation. “Cascade screening is a powerful, proven method to improve early diagnosis of FH and reduce preventable heart attacks and strokes. Together, we are poised to make this life-saving screening more accessible, ultimately safeguarding the health of future generations and reducing the burden of cardiovascular disease.”

Professor Zahid Ahmed, Program Lead for DISCOVER FH commented: “We are delighted to work with GENinCode  and implement LIPID inCode® for the diagnosis and treatment familial hypercholesterolemia. The added benefit of easy sample collection, improved test turnaround times at a reduced cost will help us deliver the Lipid inCode test in our practice, and we welcome this approach to help us deliver this first phase of the plan to reduce the onset of cardiovascular disease.”  

FH is an inherited condition, affecting about 1 in every 250 individuals globally. If a person has FH, there is a 50% chance that their children, siblings, and parents also carry the familial variant. People with FH have extremely high low-density lipoprotein-cholesterol (LDL-C, aka “bad cholesterol”) from birth which dramatically increases their risk of atherosclerotic cardiovascular disease (ASCVD) at a young age. ASCVD is cardiovascular disease as a result of cholesterol deposits in the arteries and includes heart attack, angina, the need for stents and bypass surgery, stroke, peripheral artery disease, and even sudden cardiac death. Fortunately, treatment with cholesterol-lowering drugs can significantly reduce this risk.

Unfortunately, less than 30% of people with FH in the US have been identified, despite the efforts of the Centers for Disease Control and Prevention (CDC) to prioritize FH for early detection, cascade screening, and proactive treatment with cholesterol-lowering drugs. Furthermore, people with FH and their families have recognized the missed opportunities when families are not screened for FH. The standard of care for cascade screening in the US relies on healthcare providers educating FH patients on the importance of family screening with no ability to ensure this screening happens. The Family Heart Foundation is uniquely positioned to serve as a centralized coordinating office to assist and support families in need regardless of geographic location. 

Establishing an effective cascade screening strategy in the US is urgent. Without it, up to 1 million individuals with FH may remain undiagnosed and untreated, putting them at heightened risk for heart attacks, surgical interventions, and premature death. These outcomes not only devastate families, but also impose significant costs on the healthcare system and society, particularly as heart disease linked to FH often affects younger individuals.

In the UK around 7.6m people live with heart and circulatory disease, which causes 25% of all deaths annually. Cardiovascular disease (CVD) can be reduced by identifying and treating individuals at risk, and the UK National Health Service 10 Year Plan (2019) sets out to address CVD prevention, including identifying individuals with familial hypercholesterolemia. 

Matthew Walls, CEO of GENinCode PLC said: “The collaboration with the Family Heart Foundation continues to expand the use of LIPID inCode testing to identify patients at high risk of heart disease representing the largest cause of death globally. We are now extending implementation of LIPID inCode to other US institutions for the roll-out and adoption of our leading polygenic test. We look forward to supporting the Family Heart Foundation in reaching its long-term goal to diagnose patients with familial hypercholesterolemia and provide earlier risk assessment of CVD to improve health outcomes.”

1. DIrect SCreening Of RelatiVEs to Reveal FH (DISCOVER FH)

For more information visit www.genincode.com

Enquiries:

About GENinCode:

GENinCode Plc is a UK based company specialising in genetic risk assessment and prevention of cardiovascular disease. Cardiovascular disease is the leading cause of death and disability worldwide.

GENinCode operates business units in the UK, Europe through GENinCode S.L.U, and in the United States through GENinCode U.S. Inc.

GENinCode predictive technology provides patients and physicians with globally leading preventive care and treatment strategies. GENinCode CE marked invitro-diagnostic molecular tests combine clinical algorithms and bioinformatics to provide advanced patient risk assessment to predict and prevent cardiovascular disease.

About LIPID inCode®

The LIPID inCode® monogenic and polygenic test is now being clinically implemented in United States Primary and Secondary Care settings for the diagnosis of familial hypercholesterolemia (“FH”) with further information available to physicians for polygenic hypercholesterolemia (high levels of cholesterol) and coronary heart disease risk. GENinCode delivers LIPID inCode® internationally using its ‘cloud based’ SITAB system which includes detailed genetic variant classification enabling the rapid turnaround of test results (10-15 days) at reduced cost to healthcare systems.   

About Cardiovascular Disease (CVD):

Heart and circulatory disease also known as cardiovascular disease (CVD) is the leading cause of death globally, taking an estimated 17.9 million lives each year. CVD is a group of disorders of the heart and blood vessels that include coronary heart disease, cerebrovascular disease, rheumatic heart disease and other conditions. More than four out of five CVD deaths are due to heart attacks and strokes, and one third of these deaths occur prematurely in people under 70 years of age.

The most important behavioural risk factors of heart disease and stroke are unhealthy diet, physical inactivity, tobacco use and harmful use of alcohol. The effects of behavioural risk factors may show up in individuals as raised blood pressure, raised blood glucose, raised blood lipids, and overweight and obesity. These “intermediate risks factors” can be measured in primary care facilities and indicate an increased risk of heart attack, stroke, heart failure and other complications.

Identifying those at highest risk of CVDs and ensuring they receive appropriate treatment can prevent premature deaths. Access to noncommunicable disease medicines and basic health technologies in all primary health care facilities is essential to ensure that those in need receive treatment and counselling.

About Family Heart Foundation

The Family Heart Foundation^® is a nonprofit research and advocacy organization. The Foundation is a pioneer in the application of real-world evidence, patient-driven advocacy, and multi-stakeholder education to help prevent heart attacks and strokes caused by familial hypercholesterolemia (FH) and high lipoprotein(a), or Lp(a), two common genetic disorders that have an impact across generations. The Family Heart Foundation conducts innovative research to break down barriers to diagnosis and management of inherited lipid disorders; educates patients, providers, and policy makers; advocates for change; and provides hope and support for families impacted by heart disease and stroke caused by FH, HoFH, and high Lp(a). The organization was founded in 2011 as the FH Foundation. For more information, visit FamilyHeart.org and follow us on Twitter, Facebook, Instagram, LinkedIn, #KnowLpa.

2022

LIPID inCode®, tests patients to identify familial hypercholesterolemia and prevent cardiovascular disease

Oxford, UK - GENinCode Plc (AIM: GENI), the genetics company focused on the prevention of cardiovascular disease and ovarian cancer, announces its collaboration with The Family Heart Foundation®, UT  Southwestern,  and other partner members to use the LIPID inCode® monogenic and polygenic test in US Primary and Secondary Care settings for the diagnosis of familial hypercholesterolemia (“FH”) with further information available to physicians for polygenic hypercholesterolemia (high levels of cholesterol) and coronary heart disease risk.

Supported by a US Department of Defense grant, the DISCOVER FH¹ mission is to “Research to improve early diagnosis of familial hypercholesterolemia (FH) through family screening and the implementation of diagnostic tools, including in the pediatric population.” LIPID inCode® is the diagnostic tool used for identification of patients with FH and cascade screening. Cascade screening is the process of screening family members once a person is diagnosed with FH in order to identify others who may be affected. This approach can identify both adults and children early in life, allowing earlier treatment with cholesterol-lowering therapies and reductions in the risk of heart disease.

Individuals tested in the program will be identified from two US healthcare systems, UT Southwestern Medical Center and the Veteran Affairs (VA) North Texas Health Care system. After an individual is genetically confirmed to have FH, the Family Heart Foundation will directly contact at-risk family members to educate them about their risk for FH, the significance, and coordinate genetic testing.  

“Collaborating with GENinCode and partners to implement FH testing brings us one step closer to broader and more accessible cascade screening at a national level, helping to save future generations from cardiovascular disease,” said Katherine Wilemon, Founder and CEO of Family Heart Foundation. “Cascade screening is a powerful, proven method to improve early diagnosis of FH and reduce preventable heart attacks and strokes. Together, we are poised to make this life-saving screening more accessible, ultimately safeguarding the health of future generations and reducing the burden of cardiovascular disease.”

Professor Zahid Ahmed, Program Lead for DISCOVER FH commented: “We are delighted to work with GENinCode  and implement LIPID inCode® for the diagnosis and treatment familial hypercholesterolemia. The added benefit of easy sample collection, improved test turnaround times at a reduced cost will help us deliver the Lipid inCode test in our practice, and we welcome this approach to help us deliver this first phase of the plan to reduce the onset of cardiovascular disease.”  

FH is an inherited condition, affecting about 1 in every 250 individuals globally. If a person has FH, there is a 50% chance that their children, siblings, and parents also carry the familial variant. People with FH have extremely high low-density lipoprotein-cholesterol (LDL-C, aka “bad cholesterol”) from birth which dramatically increases their risk of atherosclerotic cardiovascular disease (ASCVD) at a young age. ASCVD is cardiovascular disease as a result of cholesterol deposits in the arteries and includes heart attack, angina, the need for stents and bypass surgery, stroke, peripheral artery disease, and even sudden cardiac death. Fortunately, treatment with cholesterol-lowering drugs can significantly reduce this risk.

Unfortunately, less than 30% of people with FH in the US have been identified, despite the efforts of the Centers for Disease Control and Prevention (CDC) to prioritize FH for early detection, cascade screening, and proactive treatment with cholesterol-lowering drugs. Furthermore, people with FH and their families have recognized the missed opportunities when families are not screened for FH. The standard of care for cascade screening in the US relies on healthcare providers educating FH patients on the importance of family screening with no ability to ensure this screening happens. The Family Heart Foundation is uniquely positioned to serve as a centralized coordinating office to assist and support families in need regardless of geographic location. 

Establishing an effective cascade screening strategy in the US is urgent. Without it, up to 1 million individuals with FH may remain undiagnosed and untreated, putting them at heightened risk for heart attacks, surgical interventions, and premature death. These outcomes not only devastate families, but also impose significant costs on the healthcare system and society, particularly as heart disease linked to FH often affects younger individuals.

In the UK around 7.6m people live with heart and circulatory disease, which causes 25% of all deaths annually. Cardiovascular disease (CVD) can be reduced by identifying and treating individuals at risk, and the UK National Health Service 10 Year Plan (2019) sets out to address CVD prevention, including identifying individuals with familial hypercholesterolemia. 

Matthew Walls, CEO of GENinCode PLC said: “The collaboration with the Family Heart Foundation continues to expand the use of LIPID inCode testing to identify patients at high risk of heart disease representing the largest cause of death globally. We are now extending implementation of LIPID inCode to other US institutions for the roll-out and adoption of our leading polygenic test. We look forward to supporting the Family Heart Foundation in reaching its long-term goal to diagnose patients with familial hypercholesterolemia and provide earlier risk assessment of CVD to improve health outcomes.”

1. DIrect SCreening Of RelatiVEs to Reveal FH (DISCOVER FH)

For more information visit www.genincode.com

Enquiries:

About GENinCode:

GENinCode Plc is a UK based company specialising in genetic risk assessment and prevention of cardiovascular disease. Cardiovascular disease is the leading cause of death and disability worldwide.

GENinCode operates business units in the UK, Europe through GENinCode S.L.U, and in the United States through GENinCode U.S. Inc.

GENinCode predictive technology provides patients and physicians with globally leading preventive care and treatment strategies. GENinCode CE marked invitro-diagnostic molecular tests combine clinical algorithms and bioinformatics to provide advanced patient risk assessment to predict and prevent cardiovascular disease.

About LIPID inCode®

The LIPID inCode® monogenic and polygenic test is now being clinically implemented in United States Primary and Secondary Care settings for the diagnosis of familial hypercholesterolemia (“FH”) with further information available to physicians for polygenic hypercholesterolemia (high levels of cholesterol) and coronary heart disease risk. GENinCode delivers LIPID inCode® internationally using its ‘cloud based’ SITAB system which includes detailed genetic variant classification enabling the rapid turnaround of test results (10-15 days) at reduced cost to healthcare systems.   

About Cardiovascular Disease (CVD):

Heart and circulatory disease also known as cardiovascular disease (CVD) is the leading cause of death globally, taking an estimated 17.9 million lives each year. CVD is a group of disorders of the heart and blood vessels that include coronary heart disease, cerebrovascular disease, rheumatic heart disease and other conditions. More than four out of five CVD deaths are due to heart attacks and strokes, and one third of these deaths occur prematurely in people under 70 years of age.

The most important behavioural risk factors of heart disease and stroke are unhealthy diet, physical inactivity, tobacco use and harmful use of alcohol. The effects of behavioural risk factors may show up in individuals as raised blood pressure, raised blood glucose, raised blood lipids, and overweight and obesity. These “intermediate risks factors” can be measured in primary care facilities and indicate an increased risk of heart attack, stroke, heart failure and other complications.

Identifying those at highest risk of CVDs and ensuring they receive appropriate treatment can prevent premature deaths. Access to noncommunicable disease medicines and basic health technologies in all primary health care facilities is essential to ensure that those in need receive treatment and counselling.

About Family Heart Foundation

The Family Heart Foundation^® is a nonprofit research and advocacy organization. The Foundation is a pioneer in the application of real-world evidence, patient-driven advocacy, and multi-stakeholder education to help prevent heart attacks and strokes caused by familial hypercholesterolemia (FH) and high lipoprotein(a), or Lp(a), two common genetic disorders that have an impact across generations. The Family Heart Foundation conducts innovative research to break down barriers to diagnosis and management of inherited lipid disorders; educates patients, providers, and policy makers; advocates for change; and provides hope and support for families impacted by heart disease and stroke caused by FH, HoFH, and high Lp(a). The organization was founded in 2011 as the FH Foundation. For more information, visit FamilyHeart.org and follow us on Twitter, Facebook, Instagram, LinkedIn, #KnowLpa.

2021

LIPID inCode®, tests patients to identify familial hypercholesterolemia and prevent cardiovascular disease

Oxford, UK - GENinCode Plc (AIM: GENI), the genetics company focused on the prevention of cardiovascular disease and ovarian cancer, announces its collaboration with The Family Heart Foundation®, UT  Southwestern,  and other partner members to use the LIPID inCode® monogenic and polygenic test in US Primary and Secondary Care settings for the diagnosis of familial hypercholesterolemia (“FH”) with further information available to physicians for polygenic hypercholesterolemia (high levels of cholesterol) and coronary heart disease risk.

Supported by a US Department of Defense grant, the DISCOVER FH¹ mission is to “Research to improve early diagnosis of familial hypercholesterolemia (FH) through family screening and the implementation of diagnostic tools, including in the pediatric population.” LIPID inCode® is the diagnostic tool used for identification of patients with FH and cascade screening. Cascade screening is the process of screening family members once a person is diagnosed with FH in order to identify others who may be affected. This approach can identify both adults and children early in life, allowing earlier treatment with cholesterol-lowering therapies and reductions in the risk of heart disease.

Individuals tested in the program will be identified from two US healthcare systems, UT Southwestern Medical Center and the Veteran Affairs (VA) North Texas Health Care system. After an individual is genetically confirmed to have FH, the Family Heart Foundation will directly contact at-risk family members to educate them about their risk for FH, the significance, and coordinate genetic testing.  

“Collaborating with GENinCode and partners to implement FH testing brings us one step closer to broader and more accessible cascade screening at a national level, helping to save future generations from cardiovascular disease,” said Katherine Wilemon, Founder and CEO of Family Heart Foundation. “Cascade screening is a powerful, proven method to improve early diagnosis of FH and reduce preventable heart attacks and strokes. Together, we are poised to make this life-saving screening more accessible, ultimately safeguarding the health of future generations and reducing the burden of cardiovascular disease.”

Professor Zahid Ahmed, Program Lead for DISCOVER FH commented: “We are delighted to work with GENinCode  and implement LIPID inCode® for the diagnosis and treatment familial hypercholesterolemia. The added benefit of easy sample collection, improved test turnaround times at a reduced cost will help us deliver the Lipid inCode test in our practice, and we welcome this approach to help us deliver this first phase of the plan to reduce the onset of cardiovascular disease.”  

FH is an inherited condition, affecting about 1 in every 250 individuals globally. If a person has FH, there is a 50% chance that their children, siblings, and parents also carry the familial variant. People with FH have extremely high low-density lipoprotein-cholesterol (LDL-C, aka “bad cholesterol”) from birth which dramatically increases their risk of atherosclerotic cardiovascular disease (ASCVD) at a young age. ASCVD is cardiovascular disease as a result of cholesterol deposits in the arteries and includes heart attack, angina, the need for stents and bypass surgery, stroke, peripheral artery disease, and even sudden cardiac death. Fortunately, treatment with cholesterol-lowering drugs can significantly reduce this risk.

Unfortunately, less than 30% of people with FH in the US have been identified, despite the efforts of the Centers for Disease Control and Prevention (CDC) to prioritize FH for early detection, cascade screening, and proactive treatment with cholesterol-lowering drugs. Furthermore, people with FH and their families have recognized the missed opportunities when families are not screened for FH. The standard of care for cascade screening in the US relies on healthcare providers educating FH patients on the importance of family screening with no ability to ensure this screening happens. The Family Heart Foundation is uniquely positioned to serve as a centralized coordinating office to assist and support families in need regardless of geographic location. 

Establishing an effective cascade screening strategy in the US is urgent. Without it, up to 1 million individuals with FH may remain undiagnosed and untreated, putting them at heightened risk for heart attacks, surgical interventions, and premature death. These outcomes not only devastate families, but also impose significant costs on the healthcare system and society, particularly as heart disease linked to FH often affects younger individuals.

In the UK around 7.6m people live with heart and circulatory disease, which causes 25% of all deaths annually. Cardiovascular disease (CVD) can be reduced by identifying and treating individuals at risk, and the UK National Health Service 10 Year Plan (2019) sets out to address CVD prevention, including identifying individuals with familial hypercholesterolemia. 

Matthew Walls, CEO of GENinCode PLC said: “The collaboration with the Family Heart Foundation continues to expand the use of LIPID inCode testing to identify patients at high risk of heart disease representing the largest cause of death globally. We are now extending implementation of LIPID inCode to other US institutions for the roll-out and adoption of our leading polygenic test. We look forward to supporting the Family Heart Foundation in reaching its long-term goal to diagnose patients with familial hypercholesterolemia and provide earlier risk assessment of CVD to improve health outcomes.”

1. DIrect SCreening Of RelatiVEs to Reveal FH (DISCOVER FH)

For more information visit www.genincode.com

Enquiries:

About GENinCode:

GENinCode Plc is a UK based company specialising in genetic risk assessment and prevention of cardiovascular disease. Cardiovascular disease is the leading cause of death and disability worldwide.

GENinCode operates business units in the UK, Europe through GENinCode S.L.U, and in the United States through GENinCode U.S. Inc.

GENinCode predictive technology provides patients and physicians with globally leading preventive care and treatment strategies. GENinCode CE marked invitro-diagnostic molecular tests combine clinical algorithms and bioinformatics to provide advanced patient risk assessment to predict and prevent cardiovascular disease.

About LIPID inCode®

The LIPID inCode® monogenic and polygenic test is now being clinically implemented in United States Primary and Secondary Care settings for the diagnosis of familial hypercholesterolemia (“FH”) with further information available to physicians for polygenic hypercholesterolemia (high levels of cholesterol) and coronary heart disease risk. GENinCode delivers LIPID inCode® internationally using its ‘cloud based’ SITAB system which includes detailed genetic variant classification enabling the rapid turnaround of test results (10-15 days) at reduced cost to healthcare systems.   

About Cardiovascular Disease (CVD):

Heart and circulatory disease also known as cardiovascular disease (CVD) is the leading cause of death globally, taking an estimated 17.9 million lives each year. CVD is a group of disorders of the heart and blood vessels that include coronary heart disease, cerebrovascular disease, rheumatic heart disease and other conditions. More than four out of five CVD deaths are due to heart attacks and strokes, and one third of these deaths occur prematurely in people under 70 years of age.

The most important behavioural risk factors of heart disease and stroke are unhealthy diet, physical inactivity, tobacco use and harmful use of alcohol. The effects of behavioural risk factors may show up in individuals as raised blood pressure, raised blood glucose, raised blood lipids, and overweight and obesity. These “intermediate risks factors” can be measured in primary care facilities and indicate an increased risk of heart attack, stroke, heart failure and other complications.

Identifying those at highest risk of CVDs and ensuring they receive appropriate treatment can prevent premature deaths. Access to noncommunicable disease medicines and basic health technologies in all primary health care facilities is essential to ensure that those in need receive treatment and counselling.

About Family Heart Foundation

The Family Heart Foundation^® is a nonprofit research and advocacy organization. The Foundation is a pioneer in the application of real-world evidence, patient-driven advocacy, and multi-stakeholder education to help prevent heart attacks and strokes caused by familial hypercholesterolemia (FH) and high lipoprotein(a), or Lp(a), two common genetic disorders that have an impact across generations. The Family Heart Foundation conducts innovative research to break down barriers to diagnosis and management of inherited lipid disorders; educates patients, providers, and policy makers; advocates for change; and provides hope and support for families impacted by heart disease and stroke caused by FH, HoFH, and high Lp(a). The organization was founded in 2011 as the FH Foundation. For more information, visit FamilyHeart.org and follow us on Twitter, Facebook, Instagram, LinkedIn, #KnowLpa.