HypophosphatasiaPORTRAITNCT04222452
The PORTRAIT Study
An observational study of Hypophosphatasia, run by Sheffield Teaching Hospitals NHS Foundation Trust at 1 site in United Kingdom.
Trial summary
Clinical Consequences of Adults Presenting with Hypophosphatasia with Special Focus on Gait, Bone Microstructure and Cognition: The PORTRAIT study Hypophosphatasia (HPP) is an inherited condition that leads to weak bones. Early childhood forms are severe and easily recognized. Adult forms can vary in severity. Read more about this study
- Who is it for?
- Ages 18 to 80 yearsHealthy volunteers can take part
- Conditions the study is for
- Hypophosphatasia
- How many people
- 14 participants
- Where
- 1 siteUnited Kingdom
- Study dates
- 12 Jul 2021to 28 Feb 2023
- Phase
- Observational
- Are there results?
- None posted in the registry
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 18 to 80 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Study population: Patients with HPP (cases) and healthy individuals (controls)
Who may be able to join
- HPP PATIENTS (CASES)
- Clinical diagnosis of HPP (with or without previous genetic test confirmation)
- Evidence of burden of disease (HPP) including abnormal gait, muscle weakness, pain, recurring fractures, slow healing fractures and/or bone deformities
- Age ≥ 18 years
- Able and willing to participate in the study
- Able to give written informed consent
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- HEALTHY INDIVIDUALS (CONTROLS)
- Healthy men and women with normal bone mineral density (defined as a DXA bone mineral density T- score at the lumbar spine or total hip greater than -1).
- Age ≥ 18 years
- Able and willing to participate in the study
- Able to give written informed consent
Who cannot join
- HPP PATIENTS (CASES)
- Individuals with BMI<18, or BMI>30 kg/m2
- Other conditions known to affect serum ALP and PLP
- Coeliac disease, B12 deficiency, untreated hypothyroidism, Wilson's disease
- Taking nutritional supplements containing vitamin B6 within past two weeks
- History of, or current:
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- Severe ischaemic heart disease, rheumatoid arthritis, ankylosing spondylitis, cancer (concurrent)
- History of, or current neurological diseases affecting the neuromuscular system including Parkinson's disease, CVA, muscular dystrophy, myasthenia, cerebral trauma, peripheral neuropathy
- Treatment for more than 3 months in a year or under treatment with oral corticosteroids
- History of any long term immobilization (duration greater than three months)
- Conditions or surgery which prevent the acquisition or analysis of musculoskeletal images
- Use of medications or treatment known to affect bone metabolism other than calcium/vitamin D supplementation.
- Alcohol intake greater than 21 units per week
- Pregnant or breast feeding
- HEALTHY INDIVIDUALS (CONTROLS)
- Individuals with BMI<18, or BMI>30 kg/m2
- Other conditions known to affect serum ALP and PLP
- Coeliac disease, B12 deficiency, untreated hypothyroidism, Wilson's disease
- Taking nutritional supplements containing vitamin B6 within the past two weeks
- Bilateral fractures of the distal radius and/or distal tibia
- History of, or current conditions known to affect bone metabolism and bone mineral density including diagnosed skeletal disease or arthritis, chronic hepatic or renal disease, Coeliac and/or other malabsorption syndromes, hyperparathyroidism, hyperthyroidism and/or diagnosed endocrine disorders, hypocalcaemia or hypercalcemia, diagnosed restrictive eating disorder, diabetes mellitus
- History of, or current severe ischaemic heart disease, rheumatoid arthritis, ankylosing spondylitis, cancer (concurrent)
- History of, or current neurological diseases affecting the neuromuscular system including Parkinson's disease, CVA, muscular dystrophy, myopathies, myasthenia, cerebral trauma, peripheral neuropathy
- Treatment for more than 3 months in a year or under treatment with oral corticosteroids
- History of any long term immobilization (duration greater than three months)
- Conditions or surgery which prevent the acquisition or analysis of musculoskeletal images
- Use of medications or treatment known to affect bone metabolism other than calcium/vitamin D supplementation.
- Alcohol intake greater than 21 units per week
- Conditions that currently impact on gait
- Pregnant or breast feeding
Trial locations and contacts
1 site in 1 country.
United Kingdom1 site
The University of Sheffield
Sheffield, South Yorkshire, S5 7AU
About this study
Official title: Clinical Consequences of Adults Presenting With hyPophOsphatasia With Special Focus on Gait, Bone micRosTRucture And cognITion: The PORTRAIT Study
Clinical Consequences of Adults Presenting with Hypophosphatasia with Special Focus on Gait, Bone Microstructure and Cognition: The PORTRAIT study Hypophosphatasia (HPP) is an inherited condition that leads to weak bones. Early childhood forms are severe and easily recognized. Adult forms can vary in severity. HPP is often missed by doctors or confused with osteoporosis. This is important because the usual osteoporosis treatments may be harmful to patients with HPP and increase the risk of broken bones. One of the reasons it is missed is a lack of research describing the typical features of HPP, so doctors don't recognize the signs, and don't know when or how to test for it. The PORTRAIT Study will help increase understanding of the burden of disease of HPP on patients. The aim is to examine the effects of HPP on bone structure and strength, physical functioning, cognition, and quality of life. Researchers will study adults with HPP and healthy age- and gender-matched individuals. Blood samples will be collected after an overnight fast. Researchers will use these samples to measure markers of HPP and bone health. Medical history and lifestyle, quality of life and cognitive function will be assessed using questionnaires. Bone mineral density, body composition and bone structure and strength will be measured using dual energy x-ray absorptiometry and high resolution peripheral quantitative computed tomography. Physical functioning will be assessed as participants perform a series of physical performance and gait tests. Magnetic resonance images of the lower limbs will be matched-up with the physical functioning data to create patient-specific musculoskeletal models. Cognitive function tests will be performed to assess cognition and mental health. To reveal the burden of disease of HPP, the data collected from patients with HPP will be compared to that collected from healthy controls.
Read the detailed description
Hypophosphatasia (HPP) is caused by mutations in the tissue non-specific alkaline phosphatase (TNSALP) gene with deficiency in TNSALP activity. This leads to accumulation of inorganic pyrophosphate, a potent inhibitor of bone mineralization, which causes rickets and osteomalacia, and of pyridoxal 5-phosphate (PLP) which causes seizures in neonates but no harm in adults. HPP is also associated with muscle weakness (which is very severe in perinatal and infantile forms) and early tooth loss. The most severe forms of HPP present in infancy, and were fatal until the recent development of TNSALP enzyme replacement therapy, Asfotase Alpha. Adult-onset HPP is less severe. It often presents with fractures of the femur or metatarsals, and so is likely to be misdiagnosed as osteoporosis. Correct diagnosis of HPP is important as the usual osteoporosis treatments, for example bisphosphonates, may be harmful and increase the risk of fracture.
High resolution peripheral quantitative computed tomography (HR-pQCT) is an imaging technique that allows the detailed assessment of BMD, microstructure and strength. HR-pQCT could reveal important information about the effects of HPP on bone microstructural properties.
HPP can also have a significant effect on physical functioning. In infantile HPP, motor function delay is usual but in adult-onset HPP effects on physical functioning are less apparent. These effects can be explored through the use of physical function testing and clinical gait analysis. Cognitive function may be affected by low levels of or inactivity of ALP in the neural tissue (TNALP). Patients with HPP have reported forgetfulness and 'fogginess'.
The aims of the study are to examine the effects of HPP on (i) bone structure and strength, (ii) physical functioning, (iii) cognition and (iv) quality of life (QoL). Researchers will study adults with HPP and healthy individuals. The results will help to determine if there should be a trial of a new drug treatment for adults with HPP. This study forms part of our wider programme of research into HPP.
Researchers will recruit 7 patients with childhood- or adult-presenting HPP (cases), who are known to the Metabolic Bone Clinic at the Metabolic Bone Centre (MBC), Northern General Hospital (NGH), Sheffield. Researchers will also recruit 7 healthy controls matched to the cases by gender and age. Researchers will approach first degree relatives (with their permission) of patients with HPP to offer them genetic testing for HPP. If HPP is confirmed, approach these first degree relatives to invite them to participate in the study, Fasting blood samples will be obtained for measurement of serum or plasma bone alkaline phosphatase (bone ALP), PLP, procollagen type I N-propeptide (PINP), C-terminal telopeptide (CTX) and genetic testing (if not already performed).
Medical history and lifestyle, quality of life and cognitive function will be assessed using questionnaires.
Bone mineral density (BMD) of the lumbar spine, proximal femur and whole body will be measured using dual energy x-ray absorptiometry (DXA). Whole body composition will also be determined by DXA. Trabecular and cortical BMD and bone microstructure and strength will be examining using HR-pQCT of the distal radius and tibia.
Physical functioning will also be assessed. Participants will undergo a series of physical performance tests/gait analysis tests. Chair rises (sit to stand), a timed up and go test. A 10 m walking test and a 4 stair climb will be used to assess muscle strength. A modified performance oriented mobility assessment-gait (MPOMA-G) will also be performed. Recordings of the kinematics, ground reaction forces, electromyography (EMG) data and muscle function will be made using a motion capture system. This will allow the quantification of joint kinematics and kinetics and of muscular pattern activation during the execution of a number of different motor skills. Lower limb magnetic resonance imaging (MRI), with the participants dressed in a set of MRI visible markers, will allow the registration of the MRI and physical functioning/gait data enhancing the participant's specific musculoskeletal modelling.
Cognitive function tests (a Montreal Cognitive Assessment) will be performed to assess the burden of disease of HPP on cognitive and mental health as forgetfulness and 'fogginess' have been reported by patients.
The results from the various assessments performed will be compared between the age-gender matched cases and controls using paired samples t-tests. For each test, the mean difference, 95% confidence interval and associated p-value will be reported. In the event of the normality assumption of the paired samples t-test being violated comparisons will be made using the non-parametric Wilcoxon signed rank test. The burden of disease of HPP on bone quality (i.e. BMD, bone structure and strength), mental health, cognition, QoL, pain, physical functioning and gait will be examined using Spearman Rank Correlation.
- Conditions
- Hypophosphatasia
- Keywords
- Burden of disease, Bone microstructure, Cognition, Physical functioning
- Medical subject headings
- Hypophosphatasia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Hypophosphatasia patients (HPP) | Patients with known hypophosphatasia (HPP) as diagnosed using genetic testing. | |
| Controls | Healthy individuals (controls) matched to the cases by gender and age. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Clinical consequences and disease burden of HPP on the total score (balance + Gait) achieved during the Tinetti Performance Oriented Mobility Assessment (POMA)
Differences in gait: HPP patients versus healthy controls
Measured: Through study completion, average 18 months
Secondary outcomes (2)
Clinical consequences and disease burden of HPP on volumetric Bone Mineral Density (vBMD, in g/cm3)
Differences in bone microstructure: HPP patients versus healthy controls
Measured: Through study completion, average 18 months
Clinical consequences and disease burden of HPP on the total score achieved during the Montreal Cognitive Assessment (MoCA) Test
Differences in cognitive function: HPP patients versus healthy controls
Measured: Through study completion, average 18 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted10 Jan 2020
- Study start12 Jul 2021
- Primary completion28 Feb 2023 (estimated)
- Study completion28 Feb 2023 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for HypophosphatasiaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Case-control
- Time perspective
- Cross-sectional
- Enrolment
- 14 participants (actual)
Sponsor and investigators
- Lead sponsor
- Sheffield Teaching Hospitals NHS Foundation Trust
- Sponsor type
- University, hospital or other
- Collaborators
- University of Sheffield
- Responsible party
- Sponsor
- Investigators
- Richard Eastell, MD, Principal investigator, University of Sheffield
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04222452
- Sponsor's protocol ID
- STH20707
- Acronym
- PORTRAIT
- Status last verified
- Aug 2022
- First submitted
- 23 Oct 2019
- Last updated
- 2 Nov 2022
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 2 Nov 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Clinical Consequences of Adults Presenting With hyPophOsphatasia With Special Focus on Gait, Bone micRosTRucture And cognITion: The PORTRAIT Study
- ClinicalTrials.gov ID
- NCT04222452
- Acronym / sponsor ID
- PORTRAIT / STH20707
- Conditions
- Hypophosphatasia
- Keywords
- Burden of disease, Bone microstructure, Cognition, Physical functioning
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 14 participants (actual)
- Lead sponsor
- Sheffield Teaching Hospitals NHS Foundation TrustUniversity, hospital or other
- Collaborators
- University of Sheffield
- Study start
- 12 Jul 2021 (actual)
- Primary completion
- 28 Feb 2023 (estimated)
- Study completion
- 28 Feb 2023 (estimated)
- First posted
- 10 Jan 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Clinical Consequences of Adults Presenting with Hypophosphatasia with Special Focus on Gait, Bone Microstructure and Cognition: The PORTRAIT study Hypophosphatasia (HPP) is an inherited condition that leads to weak bones. Early childhood forms are severe and easily recognized. Adult forms can vary in severity. HPP is often missed by doctors or confused with osteoporosis. This is important because the usual osteoporosis treatments may be harmful to patients with HPP and increase the risk of broken bones. One of the reasons it is missed is a lack of research describing the typical features of HPP, so doctors don't recognize the signs, and don't know when or how to test for it. The PORTRAIT Study will help increase understanding of the burden of disease of HPP on patients. The aim is to examine the effects of HPP on bone structure and strength, physical functioning, cognition, and quality of life. Researchers will study adults with HPP and healthy age- and gender-matched individuals. Blood samples will be collected after an overnight fast. Researchers will use these samples to measure markers of HPP and bone health. Medical history and lifestyle, quality of life and cognitive function will be assessed using questionnaires. Bone mineral density, body composition and bone structure and strength will be measured using dual energy x-ray absorptiometry and high resolution peripheral quantitative computed tomography. Physical functioning will be assessed as participants perform a series of physical performance and gait tests. Magnetic resonance images of the lower limbs will be matched-up with the physical functioning data to create patient-specific musculoskeletal models. Cognitive function tests will be performed to assess cognition and mental health. To reveal the burden of disease of HPP, the data collected from patients with HPP will be compared to that collected from healthy controls.
Detailed description
Hypophosphatasia (HPP) is caused by mutations in the tissue non-specific alkaline phosphatase (TNSALP) gene with deficiency in TNSALP activity. This leads to accumulation of inorganic pyrophosphate, a potent inhibitor of bone mineralization, which causes rickets and osteomalacia, and of pyridoxal 5-phosphate (PLP) which causes seizures in neonates but no harm in adults. HPP is also associated with muscle weakness (which is very severe in perinatal and infantile forms) and early tooth loss. The most severe forms of HPP present in infancy, and were fatal until the recent development of TNSALP enzyme replacement therapy, Asfotase Alpha. Adult-onset HPP is less severe. It often presents with fractures of the femur or metatarsals, and so is likely to be misdiagnosed as osteoporosis. Correct diagnosis of HPP is important as the usual osteoporosis treatments, for example bisphosphonates, may be harmful and increase the risk of fracture.
High resolution peripheral quantitative computed tomography (HR-pQCT) is an imaging technique that allows the detailed assessment of BMD, microstructure and strength. HR-pQCT could reveal important information about the effects of HPP on bone microstructural properties.
HPP can also have a significant effect on physical functioning. In infantile HPP, motor function delay is usual but in adult-onset HPP effects on physical functioning are less apparent. These effects can be explored through the use of physical function testing and clinical gait analysis. Cognitive function may be affected by low levels of or inactivity of ALP in the neural tissue (TNALP). Patients with HPP have reported forgetfulness and 'fogginess'.
The aims of the study are to examine the effects of HPP on (i) bone structure and strength, (ii) physical functioning, (iii) cognition and (iv) quality of life (QoL). Researchers will study adults with HPP and healthy individuals. The results will help to determine if there should be a trial of a new drug treatment for adults with HPP. This study forms part of our wider programme of research into HPP.
Researchers will recruit 7 patients with childhood- or adult-presenting HPP (cases), who are known to the Metabolic Bone Clinic at the Metabolic Bone Centre (MBC), Northern General Hospital (NGH), Sheffield. Researchers will also recruit 7 healthy controls matched to the cases by gender and age. Researchers will approach first degree relatives (with their permission) of patients with HPP to offer them genetic testing for HPP. If HPP is confirmed, approach these first degree relatives to invite them to participate in the study, Fasting blood samples will be obtained for measurement of serum or plasma bone alkaline phosphatase (bone ALP), PLP, procollagen type I N-propeptide (PINP), C-terminal telopeptide (CTX) and genetic testing (if not already performed).
Medical history and lifestyle, quality of life and cognitive function will be assessed using questionnaires.
Bone mineral density (BMD) of the lumbar spine, proximal femur and whole body will be measured using dual energy x-ray absorptiometry (DXA). Whole body composition will also be determined by DXA. Trabecular and cortical BMD and bone microstructure and strength will be examining using HR-pQCT of the distal radius and tibia.
Physical functioning will also be assessed. Participants will undergo a series of physical performance tests/gait analysis tests. Chair rises (sit to stand), a timed up and go test. A 10 m walking test and a 4 stair climb will be used to assess muscle strength. A modified performance oriented mobility assessment-gait (MPOMA-G) will also be performed. Recordings of the kinematics, ground reaction forces, electromyography (EMG) data and muscle function will be made using a motion capture system. This will allow the quantification of joint kinematics and kinetics and of muscular pattern activation during the execution of a number of different motor skills. Lower limb magnetic resonance imaging (MRI), with the participants dressed in a set of MRI visible markers, will allow the registration of the MRI and physical functioning/gait data enhancing the participant's specific musculoskeletal modelling.
Cognitive function tests (a Montreal Cognitive Assessment) will be performed to assess the burden of disease of HPP on cognitive and mental health as forgetfulness and 'fogginess' have been reported by patients.
The results from the various assessments performed will be compared between the age-gender matched cases and controls using paired samples t-tests. For each test, the mean difference, 95% confidence interval and associated p-value will be reported. In the event of the normality assumption of the paired samples t-test being violated comparisons will be made using the non-parametric Wilcoxon signed rank test. The burden of disease of HPP on bone quality (i.e. BMD, bone structure and strength), mental health, cognition, QoL, pain, physical functioning and gait will be examined using Spearman Rank Correlation.
Study design
- Observational model
- Case-control
- Time perspective
- Cross-sectional
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Hypophosphatasia patients (HPP) | – | –Patients with known hypophosphatasia (HPP) as diagnosed using genetic testing. |
| Controls | – | –Healthy individuals (controls) matched to the cases by gender and age. |
Who may qualify
- Ages
- 18 to 80 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- Patients with HPP (cases) and healthy individuals (controls)
Key inclusion criteria (11 listed)
- HPP PATIENTS (CASES)
- Clinical diagnosis of HPP (with or without previous genetic test confirmation)
- Evidence of burden of disease (HPP) including abnormal gait, muscle weakness, pain, recurring fractures, slow healing fractures and/or bone deformities
- Age ≥ 18 years
- Able and willing to participate in the study
Key exclusion criteria (30 listed)
- HPP PATIENTS (CASES)
- Individuals with BMI<18, or BMI>30 kg/m2
- Other conditions known to affect serum ALP and PLP
- Coeliac disease, B12 deficiency, untreated hypothyroidism, Wilson's disease
- Taking nutritional supplements containing vitamin B6 within past two weeks
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Clinical consequences and disease burden of HPP on the total score (balance + Gait) achieved during the Tinetti Performance Oriented Mobility Assessment (POMA)
Time frame: Through study completion, average 18 months
Differences in gait: HPP patients versus healthy controls
2 secondary outcomes
Clinical consequences and disease burden of HPP on volumetric Bone Mineral Density (vBMD, in g/cm3)
Time frame: Through study completion, average 18 months
Clinical consequences and disease burden of HPP on the total score achieved during the Montreal Cognitive Assessment (MoCA) Test
Time frame: Through study completion, average 18 months
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 2 Nov 2022.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Richard Eastell, MD principal investigator
University of Sheffield
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Hypophosphatasia, run by Sheffield Teaching Hospitals NHS Foundation Trust at 1 site in United Kingdom.
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 11 inclusion and 30 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: status not confirmed, as of the sponsor's last update on 2 Nov 2022. 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 United Kingdom. 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?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Clinical consequences and disease burden of HPP on the total score (balance + Gait) achieved during the Tinetti Performance Oriented Mobility Assessment (POMA) (time frame: Through study completion, average 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 2 Nov 2022.