Skip to content

Magnesium Supplements In The Treatment Of Pseudoxanthoma Elasticum (PXE)

Magnesium Supplements In The Treatment Of Pseudoxanthoma Elasticum (PXE)

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01525875
Enrollment
44
Registered
2012-02-03
Start date
2012-08-31
Completion date
2015-03-31
Last updated
2021-03-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pseudoxanthoma Elasticum

Keywords

pseudoxanthoma elasticum, calcification

Brief summary

The purpose of this study is to evaluate the effectiveness of magnesium oxide supplements on the reversal of calcium deposits in the skin, and the yellow bumps and folds of skin in subjects with pseudoxanthoma elasticum (PXE). Magnesium oxide is a dietary supplement that has been shown in some research to reduce these calcium deposits. This study consists of two parts. The first part is a year-long, double-blind, placebo-controlled study. Part two is an open-label, year-long study. In Part 1, qualified subjects will be randomized to receive either magnesium oxide supplements or placebo, in a 1:1 ratio for the first 12 months. The starting dose will be 1000 mg daily, and depending on tolerability, doses may be decreased. Baseline evaluations will be comprised of: blood tests; clinical evaluations; skin biopsy; eye examination; bone density test; and photography of skin lesions. Subjects will be evaluated at week 2, week 6, month 3, and then every 3 months during the first year. Upon completion of the first year, barring any safety concerns, all subjects will be administered magnesium oxide supplements for up to one additional year. Subjects will undergo the same evaluations/ procedures every 3 months. We hypothesize that the magnesium oxide will cause a reduction in calcifications in the subject's soft tissue/skin. Funding Source - FDA OOPD.

Detailed description

Pseudoxanthoma elasticum (PXE) is a systemic connective tissue disorder involving elastic fiber calcification and fragmentation with major clinical manifestations occurring in the cutaneous, ocular and cardiovascular systems. Calcification of the elastic fibers leads to cracks in Bruch's membrane, an elastic tissue-containing membrane that separates the vascular choroid from the retinal pigment epithelium. These are known as angioid streaks and may be the only sign of the disease for years. Retinal hemorrhage and loss of vision are common. Calcification of the internal elastic lamina of arteries results in gastrointestinal bleeding, sometimes fatal in nature. Accelerated heart disease is an additional complication. Cutaneous manifestations are characterized by the presence of yellow papules in a cobblestone pattern or plaques resembling plucked chicken-skin in flexural regions. Redundant folds of skin may develop in more advanced cases. The most frequent sites of cutaneous involvement include the neck, axillae, inguinal region, antecubital and popliteal fossae and the periumbilical area. Skin lesions provide an easy way of grading degree of calcification of elastic tissue. A clinical study of 80 subjects with a variety of cutaneous soft tissue mineralization disorders had the affected areas injected locally with magnesium sulfate while also receiving oral magnesium lactate for 4 to 6 months. About 75% of these subjects showed a significant decrease or complete disappearance of calcification. More recently, a knockout mouse model for PXE has linked a reversal in calcification to a diet high in magnesium. Mice were placed on diets that were either high or low in phosphate, high or low in magnesium, or on a controlled diet. The mice placed on the high magnesium diet did not show any evidence of connective tissue mineralization, while those on the other diets did show mineralization as characterized by calcification of the connective tissue capsule surrounding the vibrissae. Based on this information and the research linking increased magnesium levels to decreased calcification, we plan to supplement the diets of PXE patients with magnesium oxide in order to show a reduction in elastic fiber calcification in the skin and to slow the progression of the disease. Randomized subjects will be instructed to take study drug (active or placebo) for 12 months, then all subjects will receive active study drug for the following 12 months. When ingested through foods, magnesium has not demonstrated any adverse effects. When obtained through supplements, however, excessive magnesium intake has been known to result in diarrhea as well as other gastrointestinal effects such as nausea, and abdominal cramping. Large pharmacological doses of magnesium have been associated with more serious side effects, such as metabolic alkalosis and hypokalemia with the repeated daily ingestion of 30g of magnesium oxide. Hypermagnesemia may result with excessive magnesium supplement ingestion, however, it has rarely been reported in individuals with normal renal function. Study data will be analyzed using the Wilcoxon Rank Sum Test to compare changes in physician global assessment of skin lesions, evaluation of target lesions and assessment of biopsies between treatment and placebo groups. Assuming a negligible placebo response, we believe power analyses can be performed on our primary measure in 40 completed subjects as proposed in this study. Analyses will be based on intent-to-treat, with the last observation carried forward. Patients who withdraw for safety, lack of efficacy, and generally those without other documentation will in the absence of the requested 'final-visit evaluation' be assigned the highest (worst) score. A finding of significance based on the intent-to-treat analysis would be supplemented with an analysis of patients completing the trial without any protocol deviations.

Interventions

Part 1: 1000 mg elemental magnesium (given as one 800 mg capsule of magnesium oxide two times daily). Part 2: 1500 mg elemental magnesium (given as two 500 mg capsules of magnesium oxide in the morning and three 500 mg capsules of magnesium oxide in the evening).

DRUGPlacebo

1000 mg (one 500 mg capsule two times daily) of placebo.

Sponsors

Mark Lebwohl
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Male or female subject at least 18 years of age * If female, the subject is not pregnant or nursing * If female of child bearing potential, the subject has a negative urine pregnancy test at the first visit, and agrees to use an approved method of contraception (hormonal contraceptives \[birth control pills, implants \[Norplant\] or injections \[DepoProvera\]); intrauterine device (IUD); two forms of barrier methods \[condoms and diaphragm\]; or abstinence (no sexual activity) throughout the entire study * Biopsy confirmed diagnosis of pseudoxanthoma elasticum (documenting some calcification of elastic fibers) * Subject has a clinical disease severity grade of at least 1 (Poorly defined, barely visible macules) at screening. * Normal kidney function tests

Exclusion criteria

* Any subject who is pregnant or becomes pregnant during the study * Subjects with a serum creatinine greater than 1.6 mg/dL * Subjects with hypermagnesemia, hypokalemia, or idiopathic hypercalciuria * Subjects with kidney disease or renal tubular defects (eg. Fanconi's syndrome), or on dialysis * Subjects with hypothyroidism or hypoparathyroidism or primary hyperparathyroidism * Subjects with acute gout * Subjects with malabsorption, or osteomalacia * Subjects on diuretics, magnesium containing antacids, or anabolic steroids * Subjects with Cushing's syndrome * Subjects receiving lithium and those with significant psychiatric disorders that would likely interfere with participation in this study * Subjects taking anti-seizures medications and anti-arrhythmics medications * Subjects on tetracycline or metronidazole and ace inhibitors * Subjects taking cyclosporine or calcineurin inhibitors

Design outcomes

Primary

MeasureTime frameDescription
Von Kossa Staining Per Unit Area of Dermisup to 2 yearsA blinded dermatopathologist graded skin biopsies on the density of Von Kossa staining, assessed changes in the amount of calcification of elastic fibers by assessing von Kossa staining per unit area of dermis

Secondary

MeasureTime frameDescription
Number of Participants With a 1-point Decrease of Target Lesionsup to 2 yearsChanges in skin skin lesions observed through investigator evaluations and clinical photographs. The number of patients with a 1-point decrease of target lesions
LogMar2 yearsRate of disease progression - Changes observed through ophthalmologic examinations. (+) a decrease in this score indicates improvement of the disease (-) an increase in this score indicates worsening of the disease. LogMAR: logarithm of the minimum angle of resolution. The LogMAR scale converts the geometric sequence of a traditional chart to a linear scale. It measures visual acuity loss: positive values indicate vision loss, while negative values denote normal or better visual acuity.
VAS - Visual Acuity Score2 yearsRate of disease progression observed through ophthalmologic examinations.(+) an increase in this score indicates improvement of the disease (-) a decrease in this score indicates worsening of the disease. VAS ranges from 10 to 200, with higher score indicating poorer visual acuity.
Central Retinal Thickness2 yearsRate of disease progression observed through ophthalmologic examinations. (+) a decrease in this scores indicates improvement of the disease; (-) an increase in this scores indicates improvement of the disease.

Countries

United States

Participant flow

Participants by arm

ArmCount
Magnesium Oxide
Magnesium oxide capsules 800mg twice daily (total of 1000mg of elemental magnesium) for year 1. Upon completion of the first year, barring any safety concerns, all subjects were administered 2500 mg magnesium oxide (total of 1500 mg elemental magnesium) daily for up to one additional year. Subjects received 600 mg elemental magnesium oxide in the morning (taken as two 500 mg magnesium oxide capsules, each containing 300 mg elemental magnesium) and 900 mg elemental magnesium oxide in the evening (taken as three 500 mg magnesium oxide capsules, each containing 300 mg elemental magnesium).
22
Placebo
Placebo year 1. Upon completion of the first year, barring any safety concerns, all subjects were administered 2500 mg magnesium oxide (total of 1500 mg elemental magnesium) daily for up to one additional year. Subjects received 600 mg elemental magnesium oxide in the morning (taken as two 500 mg magnesium oxide capsules, each containing 300 mg elemental magnesium) and 900 mg elemental magnesium oxide in the evening (taken as three 500 mg magnesium oxide capsules, each containing 300 mg elemental magnesium).
22
Total44

Withdrawals & dropouts

PeriodReasonFG000FG001
Open-label PeriodLost to Follow-up02
Placebo-controlled PeriodWithdrawal by Subject12

Baseline characteristics

CharacteristicPlaceboTotalMagnesium Oxide
Age, Continuous49.364 years
STANDARD_DEVIATION 12.481
49.9 years
STANDARD_DEVIATION 12.5
50.409 years
STANDARD_DEVIATION 12.764
Angioid Streaks left eye
2
1 Participants2 Participants1 Participants
Angioid Streaks left eye
3
1 Participants1 Participants0 Participants
Angioid Streaks left eye
4
20 Participants41 Participants21 Participants
Angioid Streaks right eye
2 - cardiovascular
1 Participants2 Participants1 Participants
Angioid Streaks right eye
3 - Paget's
1 Participants1 Participants0 Participants
Angioid Streaks right eye
4 - secondary
20 Participants41 Participants21 Participants
Bone Mineral Density (BMD)
AP Spine
4 Participants7 Participants3 Participants
Bone Mineral Density (BMD)
Forearm
4 Participants8 Participants4 Participants
Bone Mineral Density (BMD)
Hip
5 Participants6 Participants1 Participants
Peau D'Orange left eye
3 - Mostly macules with <5 papules
3 Participants3 Participants0 Participants
Peau D'Orange left eye
4 - >= 5 papules
19 Participants41 Participants22 Participants
Peau D'Orange right eye
3 - Mostly macules with <5 papules
3 Participants3 Participants0 Participants
Peau D'Orange right eye
4 - >= 5 papules
19 Participants41 Participants22 Participants
Sex: Female, Male
Female
18 Participants32 Participants14 Participants
Sex: Female, Male
Male
4 Participants12 Participants8 Participants
Subretinal fluid left eye
N
20 Participants40 Participants20 Participants
Subretinal fluid left eye
Y
2 Participants4 Participants2 Participants
Subretinal fluid right eye
N
21 Participants41 Participants20 Participants
Subretinal fluid right eye
Y
1 Participants3 Participants2 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 220 / 22
other
Total, other adverse events
11 / 2211 / 22
serious
Total, serious adverse events
0 / 220 / 22

Outcome results

Primary

Von Kossa Staining Per Unit Area of Dermis

A blinded dermatopathologist graded skin biopsies on the density of Von Kossa staining, assessed changes in the amount of calcification of elastic fibers by assessing von Kossa staining per unit area of dermis

Time frame: up to 2 years

Population: Estimate: Estimated change from baseline and its standard error (SEM). After 1 year=M12-Baseline, After 2 year=M24-Baseline; during 2nd year =M24-M12.

ArmMeasureGroupValue (MEAN)Dispersion
Magnesium OxideVon Kossa Staining Per Unit Area of DermisAfter 1 year-0.0033 micronsStandard Error 0.0062
Magnesium OxideVon Kossa Staining Per Unit Area of Dermisduring 2nd year0.0087 micronsStandard Error 0.0062
Magnesium OxideVon Kossa Staining Per Unit Area of Dermisafter 2 years0.0054 micronsStandard Error 0.0062
PlaceboVon Kossa Staining Per Unit Area of DermisAfter 1 year0.0010 micronsStandard Error 0.0065
PlaceboVon Kossa Staining Per Unit Area of Dermisduring 2nd year0.0123 micronsStandard Error 0.007
PlaceboVon Kossa Staining Per Unit Area of Dermisafter 2 years0.0132 micronsStandard Error 0.0069
Secondary

Central Retinal Thickness

Rate of disease progression observed through ophthalmologic examinations. (+) a decrease in this scores indicates improvement of the disease; (-) an increase in this scores indicates improvement of the disease.

Time frame: 2 years

ArmMeasureGroupValue (MEAN)Dispersion
Magnesium OxideCentral Retinal ThicknessAfter 1 year2.965 µmStandard Error 0.373
Magnesium OxideCentral Retinal Thicknessduring 2nd year-4.203 µmStandard Error 3.877
Magnesium OxideCentral Retinal ThicknessAfter 2 years-1.238 µmStandard Error 3.913
PlaceboCentral Retinal ThicknessAfter 1 year-3.552 µmStandard Error 3.429
PlaceboCentral Retinal Thicknessduring 2nd year-6.796 µmStandard Error 4.123
PlaceboCentral Retinal ThicknessAfter 2 years-10.348 µmStandard Error 4.143
Secondary

LogMar

Rate of disease progression - Changes observed through ophthalmologic examinations. (+) a decrease in this score indicates improvement of the disease (-) an increase in this score indicates worsening of the disease. LogMAR: logarithm of the minimum angle of resolution. The LogMAR scale converts the geometric sequence of a traditional chart to a linear scale. It measures visual acuity loss: positive values indicate vision loss, while negative values denote normal or better visual acuity.

Time frame: 2 years

ArmMeasureGroupValue (MEAN)Dispersion
Magnesium OxideLogMarAfter 1 year-0.049 LogMarStandard Error 0.036
Magnesium OxideLogMarduring 2nd year0.027 LogMarStandard Error 0.041
Magnesium OxideLogMarAfter 2 years-0.022 LogMarStandard Error 0.049
PlaceboLogMarAfter 1 year-0.063 LogMarStandard Error 0.036
PlaceboLogMarduring 2nd year0.015 LogMarStandard Error 0.042
PlaceboLogMarAfter 2 years-0.047 LogMarStandard Error 0.05
Secondary

Number of Participants With a 1-point Decrease of Target Lesions

Changes in skin skin lesions observed through investigator evaluations and clinical photographs. The number of patients with a 1-point decrease of target lesions

Time frame: up to 2 years

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
Magnesium OxideNumber of Participants With a 1-point Decrease of Target LesionsAfter 1 year2 Participants
Magnesium OxideNumber of Participants With a 1-point Decrease of Target Lesionsduring 2nd year8 Participants
Magnesium OxideNumber of Participants With a 1-point Decrease of Target LesionsAfter 2 years9 Participants
PlaceboNumber of Participants With a 1-point Decrease of Target LesionsAfter 1 year1 Participants
PlaceboNumber of Participants With a 1-point Decrease of Target Lesionsduring 2nd year6 Participants
PlaceboNumber of Participants With a 1-point Decrease of Target LesionsAfter 2 years7 Participants
Secondary

VAS - Visual Acuity Score

Rate of disease progression observed through ophthalmologic examinations.(+) an increase in this score indicates improvement of the disease (-) a decrease in this score indicates worsening of the disease. VAS ranges from 10 to 200, with higher score indicating poorer visual acuity.

Time frame: 2 years

ArmMeasureGroupValue (MEAN)Dispersion
Magnesium OxideVAS - Visual Acuity ScoreAfter 1 year-1.124 units on a scaleStandard Error 1.141
Magnesium OxideVAS - Visual Acuity Scoreduring 2nd year0.795 units on a scaleStandard Error 0.927
Magnesium OxideVAS - Visual Acuity ScoreAfter 2 years-0.329 units on a scaleStandard Error 1.384
PlaceboVAS - Visual Acuity ScoreAfter 1 year-0.602 units on a scaleStandard Error 1.14
PlaceboVAS - Visual Acuity Scoreduring 2nd year-0.729 units on a scaleStandard Error 0.986
PlaceboVAS - Visual Acuity ScoreAfter 2 years-1.332 units on a scaleStandard Error 1.423

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026