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Personalisation may improve prostate cancer screening accuracy

Scientists have moved a step closer to genetically personalised prostate cancer screening.
The most common assessment test for the cancer, which mainly affects men over the age of 50, is prostate-specific antigen (PSA) screening which often erroneously indicates signs of the disease.
But a joint team at UC San Francisco and Stanford University, both in the US, have come up with a method they believe will make screening more accurate by calibrating PSA levels to each man’s genetics.
They say applying this type of personalisation could significantly reduce overdiagnosis and better predict aggressive disease. In addition to the regular blood-based PSA test, such customised screening would need a germline genetic test, usually conducted on blood, saliva, or cheek swab samples, to look for inherited genetic variants that affect PSA levels.
Whilst raised PSA levels can be a sign of a cancerous prostate tumour, they can also be caused by other circumstances, like infection, an enlarged prostate, inflammation or simply old age.
In a study published in Nature Medicine, UCSF researchers and their collaborators conducted a large genome-wide association study of PSA in more than 95,000 men without diagnosed prostate cancer. This identified more than 80 novel PSA- associated variants.
They set out to discover whether accounting for genetic factors that cause variations in the levels of PSA that are not attributable to cancer could help improve PSA screening.
Senior author of the study, John Witte, a professor of epidemiology and population health and of biomedical data sciences at Stanford, said: “Some men have higher PSA levels due to their genetics. They don’t have cancer, but the higher PSA level leads to a cascade of unnecessary medical interventions like biopsy.”
Linda Kachuri, a former postdoctoral scholar in the Department of Epidemiology and Biostatistics at UCSF and lead author of the study, added: “PSA levels represent the main diagnostic biomarker for prostate cancer. This test is widely used but not currently implemented as part of a formal screening programme.
“Because of its poor sensitivity and specificity, PSA testing can often lead to detecting latent disease or, in some cases, missing aggressive tumours.”
The researchers identified 128 sites in the genome that can affect a person’s inherent PSA level. They developed a way to calculate PSA that accounts for an individual’s normal genetic variations at these sites – known as a PSA polygenic score, which is a quantitative way of measuring someone’s genetic predisposition for a trait in a single value. In this case, the trait is a higher baseline PSA level.
The researchers leveraged the new data to build a genome-wide polygenic score for PSA.
The polygenic score captured each individual’s genetic predisposition to high PSA levels. The team found the polygenic score was strongly associated with PSA levels in validation cohorts and was not associated with prostate cancer. This confirmed that it reflects benign PSA variation.
To examine whether the polygenic score could improve the detection of clinically significant disease and reduce overdiagnosis, each person’s PSA values were adjusted based on their unique genetic profile.
Dr Kachuri said: “PSA values personalised in this way are more likely to reveal changes in PSA due to prostate cancer because they are corrected for the influence of inherited genetics.”
Applying a correction to PSA levels improved the accuracy of biopsy referral decisions. Roughly 30% of men could have avoided biopsy, though adjusted PSA levels would have missed approximately 9% of positive cell samples.
Most of the latter cancers were low-grade disease that did not require treatment, but the researchers admit the misclassifications point to room for improving the polygenic score.
Dr Kachuri said: “We showed that genetic correction of PSA levels has the potential to both reduce unnecessary biopsies and improve our ability to detect tumours with a more aggressive profile. We hope that our findings represent a step forward in developing informative screening guidelines and reducing the diagnostic grey area in PSA screening.”
While the study was very large, almost 90% of the participants were of predominantly European ancestry.
According to Dr Kachuri, this represents a key limitation because the composition of the study doesn’t fully reflect the patient population impacted by prostate cancer.
The team is now working on a larger study in association with the Million Veteran Program, a US-based national research project launched in 2011 looking at how genes, lifestyle, military experience, and exposures affect health and wellness in former members of the armed forces. More than 950,000 veterans have now joined the MVP.
Nearly 1.5 million new prostate cancer cases are diagnosed each year globally and it is the fifth leading cause of cancer death among men. In the US, one in nine men will be diagnosed with prostate cancer, and one in 40 will die from it.
With a disease as prevalent as prostate cancer the researchers believe even a small improvement in screening could save lives.
Dr Kachuri concluded: “We hope to be able to share findings soon from our efforts to conduct larger and more diverse studies of PSA genetics.”
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Gut-friendly foods may damage heart, charity warns
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Diabetes patients face increased risk of undiagnosed heart failure

People with diabetes may have undiagnosed heart failure that could be detected by a simple screening blood test, research suggests.
The TARTAN-HF trial found that one in four patients with diabetes who had at least one other risk factor for heart failure had undiagnosed heart failure detected through screening with a blood test and ultrasound scanning of the heart.
Experts said the findings show the extent of unrecognised heart failure in people with diabetes, and how the condition can be detected using a widely available blood test called NT-proBNP, which measures how much strain the heart is under.
They suggest a heart failure screening programme for diabetics could improve diagnosis rates, lead to earlier treatment and potentially reduce the risk of hospitalisation and death.
The study, involving 700 patients, was led by the University of Glasgow in collaboration with AstraZeneca, Roche Diagnostics, Us2.ai, NHS Greater Glasgow and Clyde and NHS Lanarkshire.
Dr Kieran Docherty, clinical senior lecturer at the University of Glasgow’s School of Cardiovascular and Metabolic Health, said: “Our results from the landmark TARTAN-HF trial identified heart failure in a large proportion of people living with diabetes, emphasising the need for a heart failure screening strategy in this group of patients.
“We know that many of the symptoms and signs of heart failure are non-specific, and may go unrecognised as potentially being due to heart failure for a long time.
“The strategy used in our trial is simple and easy to implement in clinical practice, and will aid in the early identification of heart failure in people with diabetes, and facilitate the initiation of medications that we know improve outcomes in patients with heart failure.”
The study, which began more than three years ago, involved more than 700 people with diabetes from the two health board areas who had at least one other risk factor for heart failure.
They were randomly assigned either to receive heart failure screening or to continue with their usual care.
Researchers found screening uncovered a large number of previously unrecognised cases of heart failure. Around one in four, or 24.9 per cent, of those screened were found to have the condition within six months, compared with 1 per cent in the group continuing their usual care.
The study, involving patients with type 1 and type 2 diabetes, found almost all of the participants found to have heart failure had preserved ejection fraction, which can be difficult to detect without dedicated testing.
The findings of the TARTAN-HF trial were presented at the American College of Cardiology conference taking place from 28 to 30 March in New Orleans in the US.
Dr Edward Piper, medical director at AstraZeneca UK, said: “Delayed diagnosis and treatment of heart failure in people with type 2 diabetes contributes to poor long-term outcomes. TARTAN-HF demonstrates that targeted, risk-based screening can identify previously undiagnosed heart failure in approximately one in four high-risk patients with diabetes, enabling earlier intervention with guideline-directed therapy.”
Dr Christian Simon, head of global medical affairs at Roche Diagnostics, said: “We are proud to have supported the landmark TARTAN-HF trial. These findings demonstrate the transformative power of early, accessible diagnostics like the NT-proBNP blood test.
“By identifying unrecognised heart failure in people with diabetes, we enable clinicians to initiate appropriate treatments sooner, ultimately improving patient outcomes and lives.”
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UK government announces £6.3m fund to boost men’s health

The UK has launched a £6.3m men’s health fund to back local projects aimed at helping men and boys live longer, healthier lives.
The Men’s Health Community Fund is a partnership between the Department of Health and Social Care, Movember and People’s Health Trust.
The government is contributing £3m, while the two charities are more than doubling that to take the total to £6.3m.
Grants will support community projects reaching underserved men and boys aged 16 and over, particularly in the most disadvantaged areas and at key points in their lives such as becoming a father, losing a job or retiring.
Projects could include support for new fathers, activities for men facing loneliness and social isolation, services to help young men engage with the health system, and support for men in work, out of work and moving into retirement.
The programme will bring together voluntary, community and social enterprise organisations to test new ways of reaching men who are least likely to use traditional health services.
An evaluation funded through the National Institute for Health and Care Research will assess what works and help inform future policy and delivery.
Health and social care secretary Wes Streeting said: “Too many men across the country are living shorter, less healthy lives, particularly those in our most disadvantaged communities.
“This new partnership will help men get the support they need in the places they feel most comfortable, their communities, among people they trust.
“By working with expert charities and local organisations, we can reach the men who are too often missed by traditional services and help them take better care of their mental and physical health.”
“It is a key step in delivering our first ever Men’s Health Strategy and driving forward our ambition to halve the gap in healthy life expectancy between the richest and poorest areas.”
The Men’s Health Strategy sets out plans to tackle the physical and mental health challenges men and boys face.
Men can be less likely to seek help and more likely to suffer in silence, while higher rates of smoking, drinking, gambling and drug use are damaging men’s health and affecting families, workplaces and communities.
The government is also investing £3.6m over the next three years in suicide prevention projects for middle-aged men in local communities across areas of England where men are most at risk, many of which are also among the most deprived. Suicide is one of the biggest killers of men under 50, and three-quarters of all suicides are men.
The projects will aim to break down barriers middle-aged men face in seeking support, including stigma around asking for help and a lack of awareness of what is available and how to access it.
They will be co-designed with experts and men with lived experience of mental health crises and suicidal thoughts.












