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Coronary DiseaseNORDHEARTNCT06701968

Effects of a Healthy Nordic Diet on Atherosclerosis in Patients with Coronary Heart Disease

A study testing Healthy Nordic Diet in people with Coronary Disease and Coronary Arteriosclerosis, run by Uppsala University at 1 site in Sweden.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Diet can play a key role in atherosclerosis and coronary heart disease (CHD), but little interventional data exists, and the mediators of possible anti-atherosclerotic effects of diet are unclear. Read more about this study

Who is it for?
Ages 50 to 80 years
What is being tested?
Healthy Nordic Diet
Could I receive a placebo?
No, everyone receives an active treatment
How many people
150 participants
Where
1 siteSweden
Study dates
20 Mar 2025to 30 Dec 2031
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 50 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Men and women
  • Diagnosis with MI from 2 weeks after diagnosis and with maximum 6 months after diagnosis
  • Diagnosis with CCS (e.g. stable angina pectoris)
  • Ages 50 to 80 years
  • BMI 25-40.

Who cannot join

  • Severe heart failure (NYHA classes III, IV)
  • Alcohol intake >20g/day
  • Unwillingness to follow a new prescribed diet for 18 months
  • Other diseases implying a short estimated life expectancy (e.g. severe malignant or kidney or liver disease, as judged by consenting physician).

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Emil Hagström, MD, PHD contact

46184710000

emil.hagstrom@ucr.uu.se

Fredrik Rosqvist, PHD contact

fredrik.rosqvist@uu.se

Sweden1 site, 1 recruiting
  • Cardiology clinic, Uppsala university hospital

    Uppsala

    Emil Hagström, MD, PHD, +46184710000, emil.hagstrom@ucr.uu.se

    Recruiting

Other trials in Sweden

About this study

Official title: A Healthy Nordic Diet to Reduce the Progression of Atherosclerosis in Individuals with Coronary Heart Disease: a Secondary Prevention Trial

Diet can play a key role in atherosclerosis and coronary heart disease (CHD), but little interventional data exists, and the mediators of possible anti-atherosclerotic effects of diet are unclear. The investigators will investigate if a healthy Nordic diet (HND) reduces plaque volume, coronary artery calcification (CAC), and plaque inflammation (FAI) in CHD, and examine if changes in gut microbiota may be linked to plaque progression over time. The investigators will also explore if the diet response can be predicted by the metabolic phenotype.

In total 150 CHD patients is randomized to a HND rich in unsaturated fat and fibre from plants, or to a "usual care diet" for 18 months. Plaque volume and composition is assessed by CT, and fecal microbiota composition is determined by deep metagenome shotgun sequencing. CHD and metabolic risk factors, liver fat, muscle fat and biomarkers of diet adherence (plasma fatty acids, whole-grain metabolites) are measured. Machine-learning is used to identify diet "responders" on plaque progression, based on the individual microbiome and metabolome.

If a HND reduces plaque progression, this would be novel information of clinical importance. Also, if the diet alters microbiota that are linked to plaque progression, this would be of high scientific interest. Finally, potential prediction of the diet-response would open up for more personalized treatment of atherosclerosis.

Read the detailed description

Atherosclerosis of coronary arteries is the main cause of coronary heart disease (CHD). In atherosclerosis, atherogenic lipids are deposited in the arteries to form plaques, and the larger the plaque volume, the more narrowing of the vessel. It is now feasible to directly visualize clinically relevant changes in plaque volume and composition (e.g. calcification, lipid content) by modern computed tomography (CT) angiography. Diet is a cornerstone in both primary and secondary prevention, but it is still not clear if dietary intervention can reduce coronary plaque progression as assessed by modern imaging technique.

In the Nordic countries, a promising alternative to Mediterranean diets is the Healthy Nordic diet. Controlled trials conducted in various Nordic populations have shown that healthy Nordic diets cause reduction of several key CVD risk factors such as elevated blood lipids and blood pressure, hyperglycemia, and inflammation. The Healthy Nordic diet is mainly, but not exclusively, a plant-based diet that accord with the Nordic Nutrition Recommendations (NNR 2023), e.g. is rich in vegetable fats from oils, spreads, nuts and seeds, whole-grains from rye, barley and oats, legumes, vegetables, Nordic fruits and berries but with moderate portions (2-3 times per week) of fatty fish (e.g. Salmon). The effects of a Healthy Nordic diet in a secondary preventive setting and in particular the potential impact on atherosclerosis is yet unknown. The investigators hypothesize that a Healthy Nordic Diet has anti-atherosclerotic properties that can reduce the progress of atherosclerosis and reduce key CVD risk markers and inflammation in patients with a recent MI or chronic coronary syndrome (CCS). Further, the investigators hypothesize this diet will have favorable changes on the gut microbiota, which in turn can contribute to reduced coronary plaque progression.

The overall aim is to compare the ability of a Healthy Nordic Diet versus usual care dietary advice to influence coronary plaque volume and CVD risk after 18 months in patients with MI or with CCS.

The primary aim is to investigate if a Healthy Nordic Diet can reduce plaque volume after 18 months as compared with usual care and routine dietary and lifestyle advice, and secondary aims are to investigate dietary effects on plaque composition, coronary artery calcium (CAC) and coronary inflammation (perivascular fat, fat attenuation index), as well as on ectopic fat content (e.g. liver). Exploratory aims are to investigate the dietary effects on gut microbiota, as well as on metabolomic- lipidomic- and proteomic plasma profiles. In addition, the investigators will monitor blood glucose control using wearable continous glucose monitors (CGMs) as well as Actiheart monitors to record heart ECG and activity with multiple data endpoints.

This study, named NORDHEART, is a randomized, single-blinded, parallel study including a dietary intervention group and a control group, in individuals with diagnosed MI or CCS. The investigators aim to include n=150 individuals in this trial. The majority of participants will be recruited at the Uppsala University hospital but further Swedish recruitment center in mid Sweden might be added if the recruitment rate in Uppsala is slower than expected.

Inclusion criteria include men and women with diagnosed MI from 2 weeks after diagnosis and 6 months after diagnosis, or with CCS (e.g. stable angina pectoris), ages 50 to 80 years, BMI 25-40.

The intervention diet consists of advice to follow a Healthy Nordic Diet as, and it will be advised ad libitum. Certain key food items will be provided (~5 E%) to participants in the intervention. The control group ("usual care") will receive dietary advice in accordance with routine clinical procedures at the cardiology clinic at the Uppsala academic hospital, which follows the national guidelines for lifestyle advice in CVD care.

To monitor dietary intake in both groups, 4-day food records will be conducted at baseline, 6 months, 12 months and 18 months after study entry. Plasma fatty acid composition will be measured to objectively monitor any changes in dietary fat quality, and serum alkylresorcinols will be assessed as valid biomarkers of whole-grain intake from rye and wheat.

The primary outcome is difference between the groups in change in coronary artery plaque volume from baseline to 18 months. Intention-to treat analyses will be the primary analyses.

Secondary outcomes are change in plaque composition and inflammation (perivascular fat and inflammation, coronary calcification [CAC score], liver fat and hepatic fibrosis, LDL-cholesterol, HDL-cholesterol, ApoB, triglycerides, HbA1c, inflammation markers, from baseline to 18months, and a composite of atherosclerotic cardiovascular disease events during the 18 month follow-up.

Exploratory outcomes include effects on gut microbiota, and proteins and lipids (e.g. ceramides) involved in inflammation and markers of the atherosclerotic process. In addition, prediction models using lipidomics, metabolomics, proteomics and genetics will be assessed to explore determinants of responders and non-responders to the dietary intervention, with regard to effects on plaque volume and composition.

The plaque volume and plaque composition with be assessed by novel photon-counting CT angiography (CCTA). This technique can identify and characterize subclinical atherosclerotic disease in most vascular beds, and will be assessed at baseline and 18 months.

Given the large patient group of CHD worldwide, the clinical significance of this study has large potential, especially since there is still only limited evidence to suggest that intense dietary intervention might halt the atherosclerotic progress per se.

Being tested
Healthy Nordic Diet, Usual Care
Keywords
Diet, Secondary prevention, Coronary plaque regression, Atherosclerosis, Type 2 diabetes, Coronary heart disease, Myocardial infarction, Coronary computed tomography angiography, Healthy nordic diet, NAFLD
Medical subject headings
Coronary Disease, Coronary Artery Disease, Myocardial Infarction, Diabetes Mellitus, Type 2, Atherosclerosis, Non-alcoholic Fatty Liver Disease

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Healthy Nordic DietOther

    Participants will be adviced a healthy Nordic diet and will also receive certain Nordic foods high in wholegrains and polyunsaturated fat from vegetable sources

  • Usual CareBehavioural

    Usual care lifestyle advice and national and general recommendations on diet

Study groups in NCT06701968
Study groupRoleWhat they receive
Healthy Nordic DietExperimentalDietary advice and provided with some key food items of the healthy Nordic diet
Receives: Other: Healthy Nordic Diet
Usual careActive comparatorDietary advice according to standard clinical care at the cardiology unit
Receives: Behavioral: Usual Care

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in coronary plaque volume

    Will be assessed by photon-counting CT angiography

    Measured: 18 months

Secondary outcomes (8)
  1. Change in coronary inflammation: Fat attenuation Index

    Perivascular fat will be assessed by photon counting CT angiography

    Measured: 18 months

  2. To investigate if a Healthy Nordic Diet can decrease progression of atherosclerosis Change in coronary artery calcium score (CACS)

    CACS will be assessed by photon counting CT angiography

    Measured: 18 months

  3. Change in ectopic fat (liver, heart, muscle)

    Will be assessed by photon counting CT angiography

    Measured: 18 months

  4. Change in blood glycemic control

    Will be measured in fasting state and continously using CGM

    Measured: 6, 12 and 18 months

  5. Change in plasma LDL cholesterol

    Will be assessed by routine methods at the hospital lab

    Measured: 18 months

  6. Change in systolic and diastolic blood pressure

    Measured: 6, 12 and 18 months

  7. Incident cardiovascular events

    A composite outcome will be assesed

    Measured: 18 and 30 months (12 month post intervention)

  8. Change in hepatic fibrosis

    Liver stifness and fibrosis stages assessed by Fibroscan

    Measured: 18 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Nov 2024
  2. Study start20 Mar 2025 (estimated)
  3. Primary completion30 Jun 2030 (estimated)
  4. Study completion30 Dec 2031 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Randomized Controlled Trial
Masking
Double blind
Who is masked
Investigator, Outcomes assessor
Enrolment
150 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06701968
Sponsor's protocol ID
NORDHEART trial
Acronym
NORDHEART
Status last verified
Nov 2024
First submitted
19 Nov 2024
Last updated
6 Mar 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing Healthy Nordic Diet in people with Coronary Disease and Coronary Arteriosclerosis, run by Uppsala University at 1 site in Sweden.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 6 Mar 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Sweden. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Emil Hagström, MD, PHD (46184710000, emil.hagstrom@ucr.uu.se), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in coronary plaque volume (time frame: 18 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Mar 2025; AzTrials last refreshed its copy on 8 Nov 2026.

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