Pseudoxanthoma elasticum
Other namesGrönblad–Strandberg syndrome;[1] Groenblad-Strandberg syndrome
Pseudoxanthoma elasticum of the posterior lateral neck. Note the yellowish slightly raised bumps characteristic of this condition.
SpecialtyMedical genetics Edit this on Wikidata

Pseudoxanthoma elasticum (PXE) is a genetic disease that causes mineralization of elastic fibers in some tissues. The most common problems arise in the skin and eyes, and later in blood vessels in the form of premature atherosclerosis.[2][3][4] PXE is caused by autosomal recessive mutations in the ABCC6 gene on the short arm of chromosome 16 (16p13.1).[3][5][6]

Signs and symptoms

Dermatological manifestations

Usually, pseudoxanthoma elasticum affects the skin first, often in childhood or early adolescence.[7] Small, yellowish papular lesions form and cutaneous laxity mainly affect the neck, axillae (armpits), groin, and flexural creases (the inside parts of the elbows and knees).[3][8] Skin may become lax and redundant. Many individuals have "oblique mental creases" (horizontal grooves of the chin).[9] The lesions are asymptomatic and have a stochastic pattern of growth and spread.[10]

Ocular manifestations

PXE first affects the retina through a dimpling of the Bruch membrane (a thin membrane separating the blood vessel-rich layer from the pigmented layer of the retina), that is only visible during ophthalmologic examinations.[11] This is called peau d'orange (a French term meaning "skin of the orange"). Eventually the mineralization of the elastic fibers in the Bruch membrane create cracks called angioid streaks that radiate out from the optic nerve. Angioid streaks themselves do not cause distortion of vision, even if they cross into the foveal area. This symptom is present in almost all PXE patients and is usually noticed a few years after the onset of cutaneous lesions. These cracks may allow small blood vessels that were originally held back by Bruch's membrane to penetrate the retina. These blood vessels sometimes leak, and these retinal hemorrhages may lead to the loss of central vision. Vision loss is a major issue in many PXE patients.[12][3][4]

Additionally, patients with PXE are at a greater risk of developing optic nerve head (ONH) drusen, which are calcified lesions within the optic nerve. Careful monitoring should be considered to prevent further complication, such as retinal artery occlusion and optic neuropathy.[13]

Cardiovascular manifestations

PXE is caused by mineralization in connective tissues in mainly the skin, eyes, and blood vessels.[14] As a result of mineralized buildup in the vascular wall, patients may. be at a greater risk for intermittent claudication, a condition in which cramping pain in the leg is induced by exercise, [15] and peripheral artery disease[14] Occlusions in cerebral arteries can lead to reduced or blocked blood flow, resulting in serious complications including transient ischemic attack (TIA) and stroke. Similarly, blockages in the coronary circulatory system, also called coronary artery disease may develop, leading to angina and myocardial infarction (heart attack).[16] Cerebral ischemia in PXE is caused by small vessel occlusive disease.

Other Manifestations

Although not much is known about potential gastroenterological manifestations, gastrointestinal bleeding is a rare symptom and usually involved bleeding from the stomach.

Other rare neurological complications may include intracranial aneurysms, subarachnoid and intracerebral hemorrhages.[17]

Genetics

Pseudoxanthoma elasticum has an autosomal recessive pattern of inheritance.

80% of clinical cases of pseudoxanthoma elasticum have detectable mutations in the ABCC6 gene.[18][19][20][21] Mutations in almost all parts of the gene have been described, of all types (missense, nonsense, splice alteration, insertion, small deletion or large deletion). Although there have been reports of autosomal dominant inheritance, the inheritance is typically autosomal recessive (both parents need to be carriers, and there is a 25% chance that a child will inherit both abnormal copies of the gene and therefore develop the condition).[3]

Strong genetic linkage was found with mutations in the ABCC6 gene, which codes for the ABCC6 protein, which is a membrane transporter from the large ATP-binding cassette transporter family. The protein is expressed in most organs, but mainly in the liver and kidney. ABCC6 mediates ATP release in the liver. This is the main source of circulating pyrophosphate (PPi), and individuals affected by PXE have strongly reduced plasma PPi levels, explaining their mineralization disorder.[22] One study suggested that mutations causing total absence of an ABCC6 protein caused a more severe disease,[23] but this could not be confirmed in a subsequent case series.[24] Given the variations in age of onset and severity it is likely that other unknown risk factors (genetic, environmental, and lifestyle) may be involved.[3]

Premature atherosclerosis is also associated with mutations in the ABCC6 gene, even in those without PXE.[25] A syndrome almost indistinguishable from hereditary PXE has been described in patients with hemoglobinopathies (sickle-cell disease and thalassemia) through a poorly understood mechanism.[3] In addition, there appears to be another PXE-like syndrome with a similar phenotype but as a result of problems with another gene, gamma-glutamyl carboxylase.[26] Mutations in ABCC6 can also cause generalized arterial calcification of infancy.[27] In some cases of PXE, mutations in ABCC6 cannot be found, and other genes such as ENPP1 may be implicated.[28]

Pathophysiology

In PXE, there is mineralization (accumulation of calcium and other minerals) and fragmentation of the elastin-containing fibers in connective tissue, but primarily in the midlaminar layer of the dermis, Bruch's membrane and the midsized arteries.[29] Recent studies have confirmed that PXE is a metabolic disease, and that its features arise because metabolites of vitamin K cannot reach peripheral tissues.[30] Low levels of PPi cause mineralization in peripheral tissues.[22]

Diagnosis

Histopathology of pseudoxanthoma elasticum: Fragmentation and calcification of middermal elastic fibers on Alizarin Red staining.[31]

The diagnostic criteria for PXE are the typical skin biopsy appearance and the presence of angioid streaks in the retina. Criteria were established by consensus of clinicians and researchers at the 2010 biennial research meeting of the PXE Research Consortium.[32] and confirmed at the 2014 meeting[33] These consensus criteria state that definitive PXE is characterized by two pathogenic mutations in the ABCC6 or ocular findings – angioid streaks > 1 DD or peau d’orange in an individual <20 years of age together with skin findings:

Differential diagnosis

The differential diagnosis PXE-like papillary dermal elastolysis: Small flesh-colored papules in the neck region.[31]
Histopathology of PXE-like papillary dermal elastolysis: Loss of elastic fibers in the papillary dermis and abnormal pattern in the reticular dermis (arrow)[31]
Pseudoxanthoma elasticum versus histopathological differential diagnoses
on light microscopy (LM) and electron microscopy (EM)[31]
Pseudoxanthoma elasticum LM: Mid-dermal calcification and fragmentation of elastic fibers
EM: Mineralization in elastic fiber core
PXE-like disease with coagulation deficiency LM: Middermal calcification and fragmentation of elastic fibers
EM: Mineralization in elastic fiber periphery
Hemoglobinopathies LM: Middermal calcification and fragmentation of elastic fibers
EM: Mineralization in elastic fiber core
PXE-like papillary dermal elastolysis LM: Selective elastic tissue elimination in the papillary dermis and presence of melanophages
White fibrous papulosis of the neck LM: Dermal fibrosis in papillary and mid-reticular dermis
Late-onset focal dermal elastosis EM: Decrease of elastic fibers; fragmentation of remaining fibers
LM: Accumulation of elastic fibers in mid- and reticular dermis without fragmentation or calcification
Perforating calcific elastosis LM: Middermal calcification and degeneration of elastic fibers with transepidermal elimination
Buschke-Ollendorff syndrome LM: Increased amount of hypertrophic elastic fibers in dermis
EM: Altered translucent elastic fibers
Elastosis perforans serpiginosa LM: Transepidermal or perifollicular perforating canals
Papular elastorrhexis LM: Thickening of collagen bundles next to loss and fragmentation of elastic fibers
Upper dermal elastolysis LM: Complete loss of elastic fibers in the upper dermis
Middermal elastolysis LM: Complete absence of elastic fibers in the middermis
Linear focal elastosis LM: Massive basophilic fibers; clumping of elastic fibers in papillary dermis
Elastoderma LM: Increased, intertwining thin elastic fibers in papillary and upper reticular dermis
Calcinosis cutis LM: Deposits of calcium in the dermis

Treatment

There is no confirmed treatment that directly interferes with the disease process.[5][6]

Cosmetic surgery to remove excessive skin has been used to improve aesthetic appearance in PXE patients[5] but because of the non-life-threatening nature of these symptoms, should be used with caution.[6]

One of the most critical symptom of PXE is choroidal neovascularization which can lead to deterioration of central vision. Photodynamic therapy has been used as a treatment, but this has been replaced with endothelial growth factor (VEGF) inhibitors (such as bevacizumab, ranibizumab, and aflibercept)[6] with efficacy similar to their use in treatment of age-related macular degeneration.[4]

To limit cardiovascular symptoms, reduction of cardiovascular risk factors through lifestyle changes is recommended.[6] Generally clinicians recommend avoidance of non-steroidal anti-inflammatory drugs (NSAIDS) that increase bleeding risk, such as aspirin, and ibuprofen to prevent eye and gastrointestinal bleeding.[6]

Formerly, dietary restriction of calcium was tried with no benefit, and in fact accelerated mineralization in mice.[34] There are a number of potential treatments that are currently being tested or have just undergone testing including magnesium,[35] etidronate,[36] PPi,[37] and tissue-nonspecific alkaline phosphatase inhibitors.[38]

Given that ABCC6 heterozygous mutations result in few symptoms of PXE, this disease is a candidate for gene therapy. Some initial proof-of-principle experiments have been done in mice that have relieved some of symptoms of PXE, but as with all gene therapy treatments, there are many hurdles that must be over come including insuring that the treatment will be long-lasting and reducing the risk of insertional mutagenesis and severe immune reactions.[6]

Epidemiology

The reported prevalence of pseudoxanthoma elasticum is about 1:25,000. Females are twice as likely to be affected as males. The disease occurs in all ethnicities, but Afrikaners are more likely to have PXE as a result of a founder effect (i.e., higher prevalence in the small group of people from whom Afrikaners descend).[39]

History

The first description of PXE that distinguished it from other xanthoma conditions was by Dr Ferdinand-Jean Darrier in 1896.[40] The eponym "Grönblad-Strandberg syndrome" is used in older literature, after two physicians who made further discoveries in the disease manifestations.[41]

PXE has the distinction of being the only disease for which a layperson is the discover of the mutated gene. The ABCC6 gene mutation was discovered simultaneously by four research teams, all of which published at the same time. The principal investigators were (in order of the date of publication): Jouni Uitto,[18] Arthur Bergen,[19] Charles Boyd,[20] and Klaus Lindpainter.[21] The gene was patented by Charles D. Boyd, Katalin Csiszar, Olivier LeSaux, Zsolt Urban, Sharon Terry, and assigned to PXE International by these co-inventors. Between the filing and 2013, when the Supreme Court of the United States declared that genes may not be patented.[42] PXE International freely licensed the gene to any lab for clinical testing and research. PXE International continues to hold and maintain other patents (diagnosis and treatment patents).[43][44]

PXE International, a support organization, was founded in 1995, by Patrick and Sharon Terry,[45][46][47][48] following the diagnosis of their two children. It has a registry of 4,600 affected individuals.

Images

See also

References

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External links

Classification
Congenital malformations and deformations of integument / skin disease
Genetic disorder, membrane: ABC transporter disorders
Categories