Our Research Focus
Here, you will find an overview of a selection of ongoing research projects at Driv - Center for Women's Health Research. Researchers affiliated with Driv are engaged in groundbreaking women's health research in both primary and specialist healthcare services. The research is multidisciplinary, focusing on core areas such as clinical research, translational research, biomedical research, and public health and primary care research. The text below has been translated from Norwegian to English using artificial intelligence
Main content
Early embryonic BRCA1 epimutations and female cancer
Contact person: Stian Knappskog
In early embryonic life, before any influence of the embryo’s own hormones, the differences between females and males are few. A major difference, however, is that female embryos have two active X-chromosomes during the first 4-5 days while males have one, and that the females thereafter undergo X-chromosome inactivation to secure that only one allele is active per cell. We believe that aberrant epigenetic events (epimutations) occurring before and/or during X-chromosome inactivation is an underlying cause of a large fraction of female cancers and potentially also many other female diseases.
Triple-negative breast cancer (TNBC) is the most aggressive form of breast cancer. Around 5% of cases are caused by inherited pathogenic genetic variants in the BRCA1 gene, while the vast majority remain unexplained and are considered “sporadic”. We recently made a major breakthrough, discovering that normal cells with BRCA1 epimutations are present in a low-level mosaic pattern, in 5-10% of healthy females, and that this significantly increases the risk of TNBC. Our data indicate that a staggering 20% of TNBC cases may be caused by underlying BRCA1 epimutations. Since this mosaicism affects tissues of all germ layers and is present in newborns, the epimutations must occur early during embryonic development.
The timepoint and mechanism for BRCA1 epimutations occurrence, as well as the distribution of such epimutations in the cancer prone tissues, remain unknown. To address this, we will deliver three main outputs: (i) we will identify the precise timepoint of BRCA1 epimutation occurrence, by assessing epimutation concordance in monozygotic twins with known time of split, and by single cell lineage tracing; (ii) we will determine the impact of X-chromosome dosage; (iii) we will map the spatial distribution of BRCA1-epimutated cells in normal breast tissue to reveal if they are clustered in some high-risk milk ducts or regions of the breast.
The project will open new research horizons, far beyond BRCA1 and breast cancer, as our findings will shed light on mechanisms highly relevant for other tumor suppressor genes and female cancers. The results can also be generalized as a concept beyond the field of oncology, as early embryonic epimutations may be a major undiscovered cause of many female diseases other than cancer.
Research on ovarian cancer
Contact person: Line Bjørge
Ovarian cancer affects around 500 women in Norway annually, and despite initial treatment response, most experience relapse. Our research takes a comprehensive approach to the disease, aiming to develop more precise and effective treatment strategies. Through the project portfolio Rethinking Ovarian Cancer (RETHINK), we combine advanced tumor profiling, preclinical models, antibody-based therapies, and clinical translation. We are developing 3D tissue models, multi-omics tools for deep tumor profiling, and innovative immunotherapeutic solutions, including surgery-assisted immunotherapy.
Our research team, known as INOvA (Innovative Novel Ovarian Cancer Treatment Approaches), has existed for over 15 years and is based on interdisciplinary collaboration between researchers and clinicians, supported by national and international research funding. We actively work to understand the tumor microenvironment and identify new biomarkers and treatment options that can improve precision medicine for patients with ovarian cancer.

The Dementia Research Group
Illustration: INOvA Research Portfolio (created with Biorender.com)
Early Menopause and Autoimmunity
Contact person: Eystein Husebye
The Center for Premature Menopause and Autoimmunity is a four-year research project funded by the University of Bergen, Helse Bergen, and the Trond Mohn Foundation, led by Professor Eystein Husebye.
The center researches premature ovarian insufficiency (POI), a condition where the ovaries cease to function normally before a woman reaches the age of 40, affecting approximately 3% of women. This results in early menopause and hormonal disturbances. In addition to infertility, the consequences of POI include an increased risk of cardiovascular disease, osteoporosis, dementia, and autoimmune diseases. Hormone treatment can counteract menopausal symptoms associated with POI, but there is currently no treatment to restore or improve fertility. Despite these serious health consequences for women, the cause of POI remains unknown in the majority of cases, and the disease mechanisms are understudied.
POI is a heterogeneous disorder with many different causes, where autoimmunity accounts for 3-30% of cases. In these women, the underlying cause is an immune attack on the ovaries, leading to functional damage. The gradual destruction of the ovaries provides a potential window to halt the immune attack through immunotherapy. Establishing a clear autoimmune cause for POI is therefore important but remains challenging, as ovary-specific autoantibodies have yet to be identified, highlighting the need for better diagnostic tests.
Furthermore, the mechanisms by which sex hormones modulate the immune system and influence the risk of autoimmunity are still unclear, although we and others have previously shown a high prevalence of autoimmune disease in women with POI. Exploring changes in the immune system of young women in menopause could clarify estrogen's role in the development of autoimmune diseases.
Through interdisciplinary national and international collaboration, this project aims to provide unique insights into a disease with devastating consequences for young women, uncover sex-specific features of the immune system, and bring diagnostic tools and new immunomodulatory treatments to the clinic with the goal of restoring fertility.
The project's main goal is to improve diagnostic accuracy and treatment of ovarian failure.
This will be achieved through four work packages:
(1) Identify new autoantigens and autoantibodies targeting ovarian cells in women with POI - led by André Sulen
Identifying autoantibodies that are entirely specific to the disease will enable rapid and accurate diagnosis of whether patients have an autoimmune cause behind ovarian failure and facilitate appropriate treatment. We will use a method called PhiP-seq, in collaboration with Mark Anderson (UCSF, USA), to identify potential autoantibody candidates in serum from women with POI. Findings will be verified in a laboratory setting. We will also compare results with serum from men with autoimmune diseases to ensure the antibodies are specific to women. If promising autoantibodies are found, they will be further developed to determine if they can be used for clinical diagnostics.
Once autoantibodies are identified, we will examine how their targets (antigens) are expressed in cells, including in which tissues, quantities, and in relation to local immune cells. This will enhance our understanding of how the disease progresses. We will also use other organs and publicly available datasets to determine whether this is specific to ovarian cells.
(2) Identify how estrogen deficiency contributes to pathogenic pathways in autoimmune diseases - led by Bergithe Eikeland Oftedal
To identify estrogen's influence on the immune system and how it contributes to autoimmune diseases, we will use single-cell RNA sequencing, combined with in vitro studies of primary immune cells and flow cytometry analysis of blood cells from POI patients. These exploratory studies will provide insights into estrogen's role in the development of POI and generate new hypotheses about disease mechanisms. This information is crucial for developing new treatment strategies and will inform potential immunomodulation strategies to reverse POI. The broad screening of cytokines may also identify useful biomarkers for autoimmune POI.
(3) Determine the genetic contribution to POI - led by Eirik Bratland and Elinor Vogt
We will use exome sequencing to identify the genetic contribution to POI. Exome sequencing allows for the analysis of all coding regions of the genome. By sequencing the exomes of women with autoimmune POI, researchers can identify genetic variants that may contribute to the development of the condition. This includes both known and new mutations in genes involved in ovarian function and autoimmunity. Identifying such variants can provide insights into the molecular mechanisms behind POI and potentially reveal new therapeutic targets.
After identifying genetic variants through exome sequencing, it is important to conduct functional studies to understand their biological significance. This involves investigating how the identified variants affect gene and protein function. For example, researchers may use cell culture models to study the effect of mutations on cell growth, differentiation, and survival. Functional validation is crucial to confirm that the identified variants actually contribute to POI and are not just random findings.
(4) Immunotherapy for autoimmune oophoritis - led by Marianne Øksnes and Elinor Vogt
In a previous smaller study in collaboration with the Karolinska Institute, we showed promising results for improving fertility in women with autoimmune POI using immunomodulatory therapy (rituximab), where six out of eight women experienced spontaneous menstruation, and mature eggs were harvested from four women. Three of them became pregnant. We will now expand this study into a multicenter, double-blind, placebo-controlled, randomized trial investigating the effect of immunomodulatory therapy in 40 women with autoimmune POI in Scandinavia.
We hope that positive results from this study will lead to rituximab becoming a standard treatment for women with POI.
Pregnancy, Fetal Development, and Birth
Contact Person: Cathrine Ebbing
Fertility, pregnancy, and childbirth are unique and highly central fields of women's health. In our time, declining fertility has been highlighted as a societal issue. Pregnancy and childbirth represent significant stressors and serve as an important "stress test" for women's health.
Globally, complications during pregnancy, birth injuries, and infections are conditions that impose long-term health challenges on women.
The research group for pregnancy, fetal development, and childbirth at the Department of Clinical Medicine 2 and Haukeland University Hospital aims to uncover new knowledge about women’s health from a life-course perspective. They achieve this through studies of fertility, pregnancy, fetal life, and childbirth—conditions that particularly concern women’s lives.
The research sheds light on how circumstances before and during conception, pregnancy, and the period related to birth can have consequences for women’s health and the next generation. Some of the issues addressed include lifestyle and conditions related to conception, high-risk pregnancies (including preterm births), birth injuries, and infections, as well as how women’s health in a life-course perspective is interconnected with these factors.
The research group seeks to identify targeted and personalized interventions and recommendations that can strengthen society's and women’s self-care, aiming for better lives for women.
The research group is led by Professor Cathrine Ebbing. The group is based in the Women’s Clinic at Haukeland University Hospital. Most members of the research group are physicians specializing in obstetrics and gynecology, with midwives also part of the team.
Cardiac disease in women
Contact person: Eva Gerdts
Cardiovascular diseases are one of the leading causes of premature death or reduced quality of life for women worldwide. In 2022, 23% of deaths among Norwegian women were caused by cardiovascular disease. In Norway, the most common heart conditions are atrial fibrillation and heart failure, with heart attacks being the third most common. More women than men died from heart disease caused by high blood pressure or heart failure, while fewer women died from heart attacks.
Many believe that cardiovascular diseases primarily affect men. In reality, just as many women as men live with atrial fibrillation in Norway, and more women than men live with heart failure. Current treatments are primarily developed based on research conducted on men and often work less effectively for women. Therefore, heart disease is a significant cause of reduced women’s health today, both because these are very common conditions and because we have insufficiently studied women with heart disease.
We know that risk factors for cardiovascular disease differ between women and men. While high blood pressure, obesity, smoking, diabetes, and high cholesterol increase the risk of cardiovascular disease in both sexes, high blood pressure, obesity, diabetes, and smoking have a particularly strong impact on women’s risk. Additionally, it is well-documented that pregnancy complications and several factors related to fertility predispose women to cardiovascular disease at a young age.
Research Highlights:
High Blood Pressure and Women’s Cardiovascular Health: Our research investigates why high blood pressure is more damaging to women’s hearts and arteries. Collaborating with international research partners, we have studied the hearts of women and men with high blood pressure in clinical and population studies using ultrasound examinations.
Eva Gerdts' research shows that women are more likely than men to develop changes in the heart due to high blood pressure, particularly leading to thickened heart muscle in the left ventricle and an enlarged left atrium. Furthermore, we have found that treatment for high blood pressure is less effective in reversing these heart changes in women than in men.
Blood Pressure and Heart Attack Risk: Ester Kringeland's research has demonstrated that the harmful effects of high blood pressure begin at a lower threshold in women than in men, and high blood pressure is a stronger risk factor for heart attacks in women. This underscores why high blood pressure is more damaging to women’s hearts and a major cause of cardiovascular disease and death in women.
Inflammatory Diseases and Obesity: Helga Midtbø’s research shows that having inflammatory diseases or obesity increases the risk of heart disease even further.
Long-term Effects of Obesity: Dana Cramariuc’s research recently revealed that women more often experience persistent reduced heart function after bariatric surgery compared to men.
We are now working to identify new underlying mechanisms that explain why women are more susceptible to cardiovascular damage from high blood pressure. In collaboration with our international network, we are analyzing various molecular markers in biobank samples from large patient cohorts and population studies to better understand the reasons behind the differing effects of blood pressure and obesity on women’s cardiovascular systems compared to men’s.
This includes metabolomics, proteomics, and genomic analyses. For example, Hilde Halland recently discovered that protein patterns in blood change differently with obesity in women compared to men.
Our goal is to integrate information about biomarkers, imaging markers, and clinical factors into a system that better identifies women with high blood pressure who are at particular risk of developing cardiovascular disease. These markers will reflect mechanisms that can be targeted for the development of new treatments. Additionally, we are studying how blood pressure trends throughout life affect the risk of cardiovascular disease in old age. Our research may help determine whether the same threshold for diagnosing high blood pressure should be applied to women and men.
Menopause
Contact Person: Inger Haukenes
One in three women experiences significant symptoms during menopause, leading to a considerable reduction in quality of life and contributing to increased absenteeism from work.
The silence and stigma surrounding women’s menopause have left a knowledge gap not only among women themselves but also within healthcare education, the health services, and Norwegian workplaces. This lack of awareness means that women seeking help often fail to identify their symptoms as menopause-related. Instead, symptoms like pain, low mood, headaches, or fatigue are categorized as "diffuse and generalized women’s ailments," which are also among the leading causes of sick leave for women in this age group. Women in midlife are a vital resource in the Norwegian workforce, playing a crucial role in addressing the aging population in public healthcare systems.
Many women and men aged 45 to 55 are at the peak of their careers and still considered young in the context of working life. Therefore, we cannot afford to lose women to long-term sick leave, disability assessments, or early retirement due to menopause symptoms.
Research Gaps in Menopause, Work, and Health
There is limited research on menopause, work, and health in general. In Norway, there are currently no studies specifically addressing "menopause and work." Internationally, findings suggest that information and communication about menopause in the workplace can help reduce stigma and alleviate symptoms. Although research on menopause and absenteeism is scarce, existing studies suggest reduced work capacity and a higher likelihood of sick leave. Studies also show that women with significant symptoms consider changing jobs, reducing their working hours, or leaving the workforce entirely. Having control over one’s work situation is a key factor in remaining employed.
What can help women with significant menopause symptoms remain in the workforce? Key factors include:
- Positive experiences with primary healthcare services
- Leaders knowledgeable about menopause who are willing to implement measures to reduce symptoms
- Peer support and experience-sharing among colleagues
- Increased flexibility and control over work situations
- The option to take breaks
- Practical adjustments such as temperature control, access to cold water, and breathable work clothing
The KLAR Project
The project KLAR - Women’s Health, Menopause, and Work (funded by the Grieg Foundation, 2024-2027) focuses on four key areas to increase knowledge:
Study 1 explores how menopause is experienced by women and addressed in healthcare and the workplace within the context of the Norwegian welfare state. Interviews are conducted with women both in and out of the workforce, leaders in private and public sectors, and personnel from public and private healthcare services to identify factors that support a sustainable working life for women in menopause.
Study 2 utilizes Norway’s unique health and welfare registries to examine variations in diagnosis patterns, healthcare trajectories, and absenteeism among midlife women. This study provides a broad overview that complements the in-depth insights from Study 1.
Study 3 investigates the relevance, applicability, and adaptation of European menopause workplace guidelines (EMAS) to Norwegian workplaces. Researchers will engage experts across various levels of the workforce, from employees to leaders and trade unions, to gather feedback on EMAS and work towards consensus on guidelines.
Ongoing Communication and Knowledge Sharing is a continuous effort aimed at disseminating information to businesses, organizations, healthcare services, and the public. This aspect is prioritized to meet the growing demand for knowledge about women’s health, menopause, and work.
Through these initiatives, the KLAR project aims to address the gaps in knowledge and provide practical solutions for improving women’s health and participation in the workforce during menopause.
Oral Health from a Women's Perspective
Contact person: Sivakami Rethnam Haug
Oral Health-Related Quality of Life and Gender Differences
Oral health-related quality of life refers to how an individual’s oral health impacts their overall quality of life, encompassing physical, psychological, and social aspects. It is not just about the absence of disease but also about well-being and functional capacity related to the oral cavity. Despite an excellent dental care program in Norway, supported by general dentists, specialists, and state-of-the-art equipment, a higher proportion of women than men report low oral health-related quality of life.
Women’s Unique Oral Health Needs
Women have specific needs and considerations when it comes to oral health. Hormonal fluctuations have a surprisingly significant impact on the oral cavity. Puberty, menstruation, pregnancy, menopause, and the use of contraceptive medications all influence women’s oral health.
Pain, particularly tooth pain, among women is an area that has not been adequately addressed or thoroughly researched in Norway. Pain is a subjective experience, but when it comes to toothache, women report higher levels of pain than men. A larger proportion of women experience discomfort, issues, or problems related to teeth and the oral cavity compared to men. Dental problems, pain, dentures, and other oral conditions are more commonly associated with women, who also report more emotional distress, insecurity, and stress due to these conditions.
Research Gaps in Gender and Oral Health
Research on gender differences and women’s oral health has traditionally been underprioritized. Women are more affected by conditions such as:
- Temporomandibular disorders (TMD)
- Osteoporosis
- Burning mouth syndrome
- Salivary dysfunction
- Sjögren’s syndrome and other autoimmune diseases that can impact the oral cavity
At the Department of Clinical Dentistry, we are dedicated to studying these gender differences, particularly through clinical and patient-centered research as well as dental education research. The goal is to develop more gender-specific treatment options to better meet the unique needs of women in oral healthcare.
Women and Migraine
Contact person: Marte-Helene Bjørk
Migraine is a debilitating condition for many women, yet there is limited understanding of why the disease affects some so severely or how it can be effectively prevented.
Eighteen percent of women and six percent of men experience migraines. Young girls are five times more likely than boys to develop the most severe form of the condition: chronic migraine. Society spends over a billion Norwegian kroner annually on migraine-related costs, with more than 80 percent of this due to work-related issues caused by migraines in women. Despite this significant burden, little research focuses on identifying the underlying causes or effective treatments specifically for women.
Professor Marte-Helene Bjørk, a neurologist, leads the Female Task Force at the Norwegian Center for Headache Research (NorHead), a Center for Clinical Treatment Research (FKB) funded by the Norwegian Research Council.
The researchers have collected extensive data on genetics, environmental exposures, diagnoses, medication use, academic performance, and employment statistics. The goal is to understand the factors in women’s childhood, adolescence, and adulthood that are associated with the development of severe migraines and identify the most effective treatments. Machine learning algorithms are being used to analyze these data.
Bjørk and her team are also conducting clinical trials on medications and medical treatment technologies, with a specific focus on discovering effective treatments tailored to women.
For more information, visit: NorHead.
Women with Neurological Disease and Medication Safety during Pregnancy
Contact person: Marte-Helene Bjørk
Epilepsy and Migraines Affect Up to One in Four Women of Childbearing Age
Uncertainty about the safety of medications for these conditions during pregnancy means that many women do not receive effective treatment.
Previous research has shown that some anti-seizure medications, such as valproate (marketed as Orfiril in Norway), which is effective for epilepsy and migraines, carry a high risk of birth defects such as spina bifida and neurodevelopmental disorders like autism. This has led to restrictions on its use for women across Europe unless no alternatives are available. It is essential to identify which newer and effective anti-seizure medications can be used safely by women.
Professor Marte-Helene Bjørk, a neurologist, led the SCAN AED project, which compiled extensive health registry data on all children born in the Nordic countries. Bjørk and her team examined which medications the mothers of these five million children used and what diagnoses the children later received.
Their research found that certain anti-seizure medications appear to be safe, such as:
- Lamotrigine (Lamictal)
- Levetiracetam (Keppra)
These are safe when used alone or in combination.
However, children exposed to topiramate (Topamax) during pregnancy had a significantly increased risk of both birth defects and conditions like autism and intellectual disabilities. These findings led to the introduction of a new pregnancy prevention program for topiramate in Europe in early 2023. Topiramate is used to treat migraines and epilepsy.
Impact on Clinical Guidelines
Major changes to international clinical treatment guidelines for these conditions are anticipated, ensuring safer treatment options for women.
The SCAN AED project was funded by NordForsk.
Bergen Research Group for Gynecological Cancer
The research group is led by Professor Camilla Krakstad at the Department of Clinical Science and the Centre for Cancer Biomarkers (CCBIO), University of Bergen (UiB). The group also has strong ties to the Women's Clinic at Haukeland University Hospital in Bergen.
The team focuses on gynecological cancer, with a particular emphasis on improving diagnosis and treatment for patients with uterine cancer.
The research is built on three key pillars:
- Expert Researchers: A diverse and passionate team dedicated to making discoveries that benefit patients.
- Clinical Collaboration: Strong partnerships with clinical departments enable the collection of samples and data from relevant patients.
- Engaged Patients: Positive patient participation, with individuals willingly contributing to research efforts.
The research community includes both clinicians and basic scientists, who collaborate using various methods to generate new knowledge about gynecological cancers.
Recent Achievements
- Biomarkers: The team has identified several promising biomarkers to improve diagnosis and tailor treatments more effectively.
- Clinical Studies: Contributions to clinical trials and investigations of how treatments affect patients' quality of life in the years following a cancer diagnosis.
- Imaging: Close collaboration with Professor Ingfrid S. Haldorsen's team at the Mohn Imaging and Visualization Center to explore the use of radiological data for better diagnostics.
Areas of Focus
Mechanisms of Cancer Spread and Treatment Resistance:
Use of advanced cell models and genetic analyses to study changes associated with aggressive diseas
Improving Treatment Outcomes:
Research aimed at optimizing therapeutic strategies and identifying patients who would benefit most from specific interventions.
The research group includes approximately 25 members and receives funding from:
- University of Bergen (UiB)
- Western Norway Regional Health Authority (Helse Vest)
- The Norwegian Cancer Society (Kreftforeningen)
- The Research Council of Norway (Norges forskningsråd)
- The Trond Mohn Research Foundation
The group is dedicated to advancing knowledge in gynecological cancer for the ultimate benefit of patients.

Vulvar Cancer
Contact person: Daniela Elena Costea
Cancer of the External Female Genital Organs (Vulva and Vagina): A Rare and Under-Researched Cancer
Cancers originating in the external female genital organs (vulva and vagina) are rare, with limited research dedicated to them. However, the incidence of this cancer type is steadily increasing, particularly among women under 60. In Norway, approximately 80 patients are diagnosed with these cancers annually.
Despite the heterogeneity of this disease, most patients receive the same standard treatment. Unfortunately, the prognosis remains poor due to the lack of effective treatments for locally advanced, radiation-resistant diseases or systemic disease. One of the major challenges is understanding why patients with similar disease characteristics experience differing outcomes despite undergoing the same primary treatment regimen.
Biomarkers for stratifying patients have not yet been identified for this cancer type. The research group is focused on:
- Defining biomarkers for personalized treatment.
- Establishing representative experimental models to better understand the biology of this cancer and to test new drugs.
The Role of Organoids
Organoids are three-dimensional in vitro tissue culture models that closely mimic the original tumors. They offer a promising tool for selecting personalized treatments.
One of the group’s main objectives is to establish an organoid platform for vulvar cancer, which will:
- Serve as the foundation for identifying the biological properties of these tumors.
- Help characterize potential responses to specific medications.
- The team aims to use organoids to identify treatments tailored to individual patients.
- This cutting-edge approach combines experimental pathology and clinical insights to improve outcomes for women with vulvar cancer.
This work is a collaboration between the Experimental Pathology Research Group, led by Daniela Elena Costea at the Gade Laboratory for Pathology, University of Bergen (UiB), and Professor Line Bjørge at the Women’s Clinic, Haukeland University Hospital, and the Department of Clinical Medicine 2, UiB.
For further insights, read:"Printer mini-svulster i 3D for å finne medisin mot vulvakreft | Norske Kvinners Sanitetsforening (sanitetskvinnene.no) (In Norwegian).
Myalgic encephalomyelitis/ chronic fatigue syndrome (ME/CFS)
Contact person: Karl Johan Tronstad
The research group is based at the Department of Biomedicine (IBM) at the University of Bergen. They conduct biomedical laboratory studies and advanced analyses of patient samples to investigate molecular and cellular disease mechanisms. A key focus is the critical role of energy metabolism in maintaining cellular health.
An important area of research for the group is myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). This debilitating condition disproportionately affects women compared to men. The underlying disease mechanism remains unknown, and there are currently no biomarkers or effective treatments.
The group collaborates closely with the research team led by Øystein Fluge and Olav Mella at the Cancer Department of Haukeland University Hospital, which conducts clinical trials aimed at finding treatments for ME.
Link Between ME and Infections
ME often develops as a long-term consequence of an infectious illness. Several types of infections have been associated with ME, including mononucleosis and COVID-19. One prominent theory suggests that such infections cause a persistent immune system dysfunction, which subsequently impacts various organs and systems in the body.
There are parallels with other chronic diseases driven by similar mechanisms, many of which also predominantly affect women. It is plausible that gender differences in the immune system and/or energy metabolism could explain why 70-80% of ME patients are women.
The group’s objective is to gain a deeper understanding of the mechanisms underlying ME. This knowledge could pave the way for the development of biomarkers and treatments for the condition.
Lipedemia
Contact person: Hildur Skulardottir
Lipedema is a chronic disease that almost exclusively affects women and is characterized by painful subcutaneous fat tissue in the areas around the hips, thighs, calves, and, in some cases, arms. The condition typically develops in connection with puberty, pregnancy, or menopause. Patients exhibit a symmetrical fat distribution, with a slim upper body and disproportionately large thighs and calves. The patient group reports a sensation of heaviness in the legs and a tendency to bruise easily in affected areas. Studies show that individuals with lipedema experience a reduced quality of life, an increased prevalence of mental health issues, and a decreased level of functioning. The main symptom of lipedema is pain in the fatty tissue, but the exact cause of this pain remains unknown.
There is currently no curative treatment for lipedema, and there is a lack of solid evidence to provide knowledge-based recommendations for different treatment options, whether conservative or surgical. Some studies suggest that surgical treatment in the form of liposuction can reduce pain and improve quality of life, but these studies do not meet sufficient scientific standards to form the basis for evidence-based treatment recommendations.
The study Surgical Treatment of Lipedema in Norway is a national multicenter study conducted at the request of the Ministry of Health and Care Services. The study is led by Haraldsplass Deaconess Hospital, in collaboration with Telemark Hospital (Health South-East), St. Olavs Hospital (Health Central), and the University Hospital of North Norway (Health North).
The purpose of the lipedema study is to investigate the effect of liposuction on pain and quality of life in women with lipedema. Additionally, the study aims to evaluate the use of pulsation therapy for non-surgical treatment of lipedema and to conduct a comprehensive mapping of the patient population. Furthermore, the study hopes to provide more information about the need for conservative treatment and the appropriate duration of such treatment.
The current knowledge base regarding lipedema is highly insufficient, making the results of this study significant not only for patients in Norway but also internationally. Our goal is for the study’s findings to contribute to increased knowledge and improved treatment for women with lipedema.
Bone Fractures
Contact person: Bård Bogen
Bone mineral density increases as we grow from childhood to adulthood. After reaching adulthood, it gradually declines, making bones more prone to fractures. This is particularly true for women, as the loss of bone mass accelerates after menopause. For many, the loss of bone mass becomes significant enough to be classified as osteoporotic or having brittle bones. Osteoporotic fractures, often referred to as low-energy fractures, occur from minor incidents, such as a fall from standing height. Research shows that women experience a much higher incidence of common low-energy fractures, such as wrist fractures, spinal compression fractures, and hip fractures, compared to men. These fractures can significantly impact health and functional ability, especially with advancing age.
Impact of Osteoporosis Diagnosis
Receiving a diagnosis of osteoporosis or experiencing a fracture can be life-changing. Many individuals significantly reduce their activity levels due to fear of further fractures. However, research indicates that maintaining an active lifestyle is crucial—not only for overall health but also because physical activity strengthens bones. There is a clear need for increased expertise on how to advise older individuals with low-energy fractures on safe exercise and physical activity.
Risk of Subsequent Fractures
Studies further show that individuals who have suffered one low-energy fracture are significantly more likely to experience additional fractures. It is therefore essential that these individuals undergo bone density assessments to evaluate their risk. If osteoporosis is diagnosed, appropriate treatment—such as osteoporosis medication and fall-prevention training—can be initiated.
Fracture Liaison Services (FLS)
Many hospitals worldwide have established Fracture Liaison Services (FLS) to identify older patients with fractures and refer them for assessment and treatment. Research shows that these services can significantly reduce the risk of subsequent fractures. In Norway, several hospitals offer such services, although Bergen does not yet have one.
Developing FLS in Bergen
The Bergen Geriatric Research Group is working to develop such services in Bergen. A pilot project is currently underway at Haraldsplass Deaconess Hospital, where individuals admitted to the orthopedic department are identified and offered bone density measurement and fall risk assessment. The primary goal of the pilot is to gain practical experience and generate insights into how an FLS can be effectively implemented in Bergen.
Additionally, funding has been applied for to support a Ph.D. project aimed at developing a training and information program for postmenopausal women with osteoporosis and osteoporotic fractures.
Aging and cognitive function
Contact person: Ragnhild Eide Skogseth
Dementia, including Alzheimer's disease, affects both men and women, but women have a higher prevalence. Several factors contribute to this, including hormonal changes related to menopause. Reduced estrogen production after menopause has been associated with an increased risk of cognitive decline, as estrogen has a neuroprotective effect on the brain. This hormone plays a key role in synaptic plasticity and neuroprotection, and a reduction in estrogen levels may therefore contribute to the development of dementia in women.
Women often develop Alzheimer's disease later than men, but the disease course tends to be more severe. Women are also more likely to be primary caregivers, which can lead to chronic stress, shown to have a negative impact on cognitive health. Furthermore, women often seek medical help earlier than men, which may result in a faster diagnosis but also increased anxiety and concern.
Although there is currently no cure for dementia, early diagnosis, lifestyle interventions such as physical activity, diet, and mental stimulation, have been shown to positively impact cognitive health. Increased research into gender-specific factors in dementia is needed to develop more precise treatment and prevention strategies for women.
Haraldsplass Diaconal Hospital, in collaboration with NeuroSysmed, is conducting research on dementia and recruiting patients for both clinical trials and observational studies to improve treatment and gain deeper insight into the disease mechanisms.

Sjögren's disease
Contact person: Silke Appel
In the laboratory, we have studied how to influence certain immune cells, known as dendritic cells, to suppress diseased blood cells. This could represent a potential new treatment method for Sjögren’s syndrome. Many of our studies have focused on analyzing salivary gland biopsies, which are crucial both for diagnosing Sjögren’s disease and classifying patients.

Pronounced inflammation in the salivary glands has been shown to correlate with a more active disease type. The first study describing the local production of autoantibodies in the salivary glands was conducted in Bergen. Later, we examined fat tissue in the salivary glands and demonstrated that it can influence local inflammation.

In approximately one-quarter of all patients with Sjögren’s disease, there is an organization of inflammatory cells in the salivary glands. When we linked this to a specific subgroup of Sjögren’s patients, we found an association with an increased risk of lymphoma, one of the more serious consequences of Sjögren’s disease. These patients are now monitored with more frequent clinical check-ups to detect lymphoma as early as possible and initiate tailored treatment.
In collaboration with groups in France, Sweden, and Italy, we have explored salivary gland ultrasound. This imaging technique is now used in clinical practice as an aid in diagnosis and to monitor inflammatory changes in the salivary glands over time without requiring new tissue biopsies.

Over the past 30 years, we have made significant discoveries by utilizing blood, saliva, and tissue from our patients. This has inspired us to follow patients over many years, including with pancreatic ultrasound. We have extensive collaborations within Norway, Scandinavia, Europe, and globally, particularly in the USA. Together, we have made numerous important findings that will contribute to future targeted treatments for the disease.
Our research has received funding from Broegelmann's Legacy, Helse Vest, the Norwegian Research Council, the European Union (EU), Trond Mohn, and other contributors. In 2015, the Sjögren research community in Bergen organized the International Sjögren’s Congress, bringing together approximately 300 Sjögren’s researchers from around the world.
Thank you to all who, through participation in our research projects, have helped contribute to new knowledge about Sjögren’s syndrome!
Silke Appel
Kathrine Skarstein
Malin Jonsson
Daniel Hammenfors
Roland Jonsson
Johan G. Brun
Four Key Research Areas in Women's Health
Biomedicine
For a number of diseases that affect women more than men, there is a significant need for knowledge about causes and mechanisms. The center aims to strengthen laboratory-based biomedical research on gender-related factors and connections in biological data, as well as through experimental studies. Research groups affiliated with the center use a variety of approaches and methods involving molecular and cellular biology, animal research, and data processing techniques to better understand diseases. The various research themes include, among others, metabolism, inflammation, and the immune system, in relation to cancer and other diseases such as cardiovascular diseases and ME/CFS.
Research area leader: Karl Johan Tronstad, Professor, Faculty of Medicine, University of Bergen
Clinical research
Clinical research conducted by research groups affiliated with Driv has had a particular focus on gynecological cancers, such as cervical cancer, endometrial cancer, and ovarian cancer. The research results have been central to improving diagnostics, early treatment, and long-term prognoses for patients with these diseases. The studies have identified risk factors and evaluated methods such as advanced imaging and biomarkers, as well as new treatment approaches including surgery, radiation therapy, and chemotherapy. The research has enhanced clinical practice through the development of new guidelines for patient care.
Research area leader: Jone Trovik, Senior Consultant at the Women's Clinic and Professor, Haukeland University Hospital and Faculty of Medicine, University of Bergen
Translational research
Translational research takes laboratory findings and turns them into clinical solutions such as new medications, treatments, and diagnostic tools. To improve women's health, bridging the gap between science and clinical practice is crucial. The academic community affiliated with Driv consists of clinicians and basic researchers who collaborate to explore gynecological cancers. Research groups associated with the center identify biomarkers for improved diagnosis and treatment, participate in clinical trials, enhance diagnostics using radiological data, and utilize advanced cell models and genetic analyses to understand cancer spread and resistance.
Research area leader: Camilla Krakstad, Professor and Head of the Bergen Gynecological Cancer Research Group, Faculty of Medicine, University of Bergen
Public health research and primary care
Public health research conducted by the research group affiliated with Driv focuses on understanding and improving women's health from a societal perspective. It explores how social, cultural, and structural factors influence women's sick leave and their interactions with the healthcare system. The research group works to identify how the healthcare system and working life manage menopause, both at the individual and aggregate levels. The various approaches involve adapting European guidelines for menopause in the workplace (EMAS) to the Norwegian working environment and disseminating knowledge about menopause in the workplace for use, among other things, in guidance for managers and employees. The research group contributes to identifying health disparities and shaping policies to promote better health outcomes and workforce participation for women.
Research area leader: Inger Haukenes, Associate professor, Faculty of Medicine, University of Bergen, and Senior Researcher II at NORCE