Perspectum

Perspectum Innovating medical imaging in Oxford - where tradition meets technology. AI-driven, patient-focused, advancing healthcare.

Perspectum is a medical diagnostics company, and developer of LiverMultiScan, a non-invasive MRI based test for liver disease. Follow the link to our website to discover more about advanced liver visualisation

We hope to use this page to keep in touch with people interested in us, as well as the wider liver community.

Three questions about one liver. How much fat is present. How much structural damage has accumulated. How much disease a...
28/08/2026

Three questions about one liver. How much fat is present. How much structural damage has accumulated. How much disease activity is present, and whether it is changing.

Over the past few weeks we have made the case that no single measurement answers all three, and that activity is the dimension most often missing.

LiverMultiScan answers two of those questions directly, in one non-contrast MRI scan with an acquisition time of ~5 minutes. cT1, developed and evaluated against liver biopsy, provides a quantitative measure of liver disease activity. PDFF quantifies liver fat. The same scan also reports LIC, liver iron concentration.

Disease activity, quantified.

Fibrosis describes what has accumulated. cT1 describes what is happening now. Clinical decisions are stronger when you know both.

Learn more about LiverMultiScan: https://perspectum.com/products/livermultiscan/

Chronic conditions rarely develop in one organ at a time. Yet most health assessments still look at organs one by one.To...
18/08/2026

Chronic conditions rarely develop in one organ at a time. Yet most health assessments still look at organs one by one.

Today we are announcing a partnership with Singapore Institute of Advanced Medicine Holdings Ltd (SAM), delivered through its Advanced Medicine Imaging (AMI) subsidiary, to bring CoverScan to patients in Singapore.

CoverScan quantifies the health of the liver, heart, kidneys, and pancreas in a single, non-contrast MRI scan, generating one unified, quantitative report of systemic health and metabolic risk. AMI's physicians will review CoverScan reports alongside their clinical assessments to support patient care and health screening pathways.

Read the full announcement: https://perspectum.com/singapore-institute-of-advanced-medicine

F4 is one fibrosis category. It is not one biological state.Cirrhosis describes advanced architectural and structural ch...
14/08/2026

F4 is one fibrosis category. It is not one biological state.

Cirrhosis describes advanced architectural and structural change, and that remains central to prognosis and clinical management. But fibrosis stage alone does not fully characterize what is happening in the liver now.

Two people with the same fibrosis stage may have different levels of ongoing tissue injury and inflammatory activity, different patterns of extracellular-matrix remodeling, and different trajectories of progression, stability, or regression.

Fibrosis stage helps describe what the liver has become. Complementary assessment may be needed to characterize the disease-related tissue changes that remain active or continue to evolve.

This distinction can matter as we are making clinical decisions.

How should we assess both accumulated structural burden and ongoing tissue change?

If the right measurement depends on the clinical question, here is one that fibrosis assessment alone may not fully answ...
12/08/2026

If the right measurement depends on the clinical question, here is one that fibrosis assessment alone may not fully answer: is disease activity elevated despite low liver stiffness?

In a real-world cohort of patients evaluated for chronic liver disease, those with low fibrosis risk by MRE (800 ms) had a higher risk of biochemical worsening over approximately 12 months than the other MRE/cT1 groups (HR 3.1).

Low liver stiffness and elevated disease activity can therefore coexist. Elastography assesses liver stiffness associated with fibrosis risk, while cT1 provides a quantitative measure of liver disease activity.

This is where cT1 may add complementary information, helping identify risk that fibrosis assessment alone may not reveal.

Learn more about LiverMultiScan: https://perspectum.com/products/livermultiscan/

Read the full paper, "Real-World Assessment of Liver Corrected T1 and Magnetic Resonance Elastography in Predicting Liver Disease Outcomes": https://pubmed.ncbi.nlm.nih.gov/40810289/

Coexisting liver disease complicates the treatment of psoriatic disease. The BALANCE study has been designed to examine ...
10/08/2026

Coexisting liver disease complicates the treatment of psoriatic disease. The BALANCE study has been designed to examine this problem, and the first UK patient has now been recruited.

People with psoriasis and psoriatic arthritis are at increased risk of liver disease, in part because of the medicines used to manage their condition. When there is concurrent liver disease, treatment options narrow, and conventional assessment provides limited scope for monitoring change over time.

BALANCE is led by the Oxford Clinical Trials Research Unit's Experimental Medicine and Rheumatology group. The study will use CoverScan, our multi-organ MRI analysis solution, to quantify liver disease activity (with imaging biomarker cT1) after treatment with Bimekizumab, a drug that blocks inflammatory proteins used in routine care for psoriatic disease. CoverScan will also quantify the fat, structure and function in other organs (fat for the heart, pancreas, and across the body; inflammation and fibrosis in the heart, pancreas and kidneys; and other measures of volume and function in the heart and skeletal muscle).

BALANCE aims to recruit 30 participants with psoriasis or psoriatic arthritis across four NHS sites in England, each scanned at baseline and again at six months, producing paired organ-level measurements before and during treatment.

The study is significant for three reasons. It applies multi-organ imaging in rheumatology, extending our evidence base beyond hepatology into immune-mediated disease. It positions quantitative imaging endpoints within an interventional trial, where organ-level change must be measured repeatedly and reproducibly. It is conducted within routine NHS care, the setting in which such measurements must ultimately perform.

Where concurrent disease is present, single-organ assessment leaves clinically relevant questions unanswered. Studies of this kind are how the evidence for whole-body assessment is established.

Read more from OUH: https://www.ouh.nhs.uk/news/articles/2452/

An imaging endpoint you can't reproduce isn't really an endpoint.In cardiovascular trials, imaging endpoints drive go/no...
04/08/2026

An imaging endpoint you can't reproduce isn't really an endpoint.

In cardiovascular trials, imaging endpoints drive go/no-go decisions, dose selection and regulatory submissions. Yet variability between scanners, sites and readers can obscure true treatment effects.

Quantitative cardiac MR has a strong evidence base across cardiac structure, function and tissue characterization. Several measures register change earlier than clinical or serum biomarkers, and the precision of the method supports smaller sample sizes and deeper phenotyping of heterogeneous cohorts. But that value only holds if the measurement is consistent everywhere it's taken.

That's why we don't just centralize image reading. Our support starts at the site, through protocol design, technologist training and real-time image quality review, with standardized analysis and locked algorithms holding it downstream.

With pivotal cardiovascular trials averaging around $157M, endpoint variability is one of the few components still addressable before enrollment closes.

Our new white paper makes the case for endpoints that are quantitatively comparable, not just centrally read.

Read it here:https://perspectum.com/wp-content/uploads/2026/03/Perspectum_Streamlining_Cardiovascular_Clinical_Trials.pdf

If the same fibrosis stage can coexist with different levels of disease activity, the starting question is not simply wh...
30/07/2026

If the same fibrosis stage can coexist with different levels of disease activity, the starting question is not simply which test to run. It is what we need to measure.

One liver can raise three distinct questions:

How much fat is present?

How much structural damage has accumulated?

How much disease activity is present... and is it changing?

No single measurement answers all three.

MRI-PDFF quantifies liver fat. Fibrosis assessment characterizes accumulated structural burden and long-term risk. cT1 provides a quantitative measure of disease activity, adding complementary information about what is happening now in the liver as well as longitudinal tissue change.

These are not competing answers to the same question. They describe different dimensions of the same liver, and together can provide a more complete picture.

The question should determine the measurement.

Learn more about LiverMultiScan: https://perspectum.com/products/livermultiscan/

Two patients. Similar fibrosis stage. Different levels of disease activity.Fibrosis tells us how much structural damage ...
21/07/2026

Two patients. Similar fibrosis stage. Different levels of disease activity.

Fibrosis tells us how much structural damage has accumulated. It remains essential for staging, prognosis and long-term risk assessment.

But fibrosis burden alone does not fully describe what is happening in the liver now.

Disease activity arises from interacting biological processes including inflammation, cellular injury and active fibrogenesis. The downstream tissue consequences of these processes can differ substantially between patients with similar fibrosis.

That is why different biomarkers answer different clinical questions.

Fibrosis assessment characterizes accumulated structural burden. MRI-PDFF quantifies the amount of fat. cT1 complements these by measuring the level of liver disease activity.

Together, structural assessment and quantitative tissue characterization can provide a more complete picture of MASLD and how it changes during treatment.

Learn more: https://perspectum.com/products/livermultiscan/

Not all body fat carries the same risk, and the dangerous kind doesn't show up on the scales.In 75,331 UK Biobank partic...
15/07/2026

Not all body fat carries the same risk, and the dangerous kind doesn't show up on the scales.

In 75,331 UK Biobank participants, MRI-measured visceral fat predicted type 2 diabetes, liver, cardiovascular and kidney events beyond BMI. And one MRI slice matched a full abdominal 3D scan.

Standard checks can miss liver disease in children. Imaging can reveal it.In Mexico's METCOG cohort, ~1 in 7 children sc...
15/07/2026

Standard checks can miss liver disease in children. Imaging can reveal it.

In Mexico's METCOG cohort, ~1 in 7 children scanned showed signs of MASLD, often without symptoms.

Observational study. Luis presents at ICO 2026: https://icocongress.com/programme-overview/

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