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HypophosphatasiaPORTRAITNCT04222452

The PORTRAIT Study

An observational study of Hypophosphatasia, run by Sheffield Teaching Hospitals NHS Foundation Trust at 1 site in United Kingdom.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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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

Other trials in United Kingdom

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.

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 groups in NCT04222452
Study groupRoleWhat they receive
Hypophosphatasia patients (HPP)Patients with known hypophosphatasia (HPP) as diagnosed using genetic testing.
ControlsHealthy 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.

  1. 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)
  1. 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

  2. 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.

  1. First posted10 Jan 2020
  2. Study start12 Jul 2021
  3. Primary completion28 Feb 2023 (estimated)
  4. Study completion28 Feb 2023 (estimated)

Resources

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)
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

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.

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