Open access peer-reviewed chapter

Hypophosphatasia: A Systemic Skeletal Disorder Caused by Alkaline Phosphatase Deficiency

By Hideo Orimo

Submitted: November 2nd 2016Reviewed: August 17th 2017Published: December 20th 2017

DOI: 10.5772/intechopen.70597

Downloaded: 258

Abstract

Hypophosphatasia (HPP) is an inherited systemic bone disease caused by the deficiency of tissue-nonspecific alkaline phosphatase (TNAP). HPP is classified into six forms and the symptoms of HPP vary depending on the form. The pathophysiology of HPP is basically due to a defect of bone mineralization. TNAP is encoded by the ALPL gene, and the TNAP protein expressed in bone, kidney, liver, and neuronal cells and is linked to the cell membrane via a glycosylphosphatidylinositol anchor. TNAP is an ectoenzyme hydrolyzing phosphate compound such as inorganic pyrophosphate. TNAP plays an important role in mineralization of hard tissues. Defect of mineralization process causes hypomineralization of hard tissues, which leads to rickets or osteomalacia and dental manifestations. In addition, hypomineralization of the ribs results in respiratory failure in the severe forms, which is the main cause of death. Inheritance of HPP is autosomal recessive, but autosomal dominant cases have been reported in the milder forms. To date, a total of 335 mutations in the ALPL gene have been reported, and mutation sites are scattered throughout the gene. Recent development of enzyme replacement therapy has opened up a new vista on the treatment of this previously untreatable disease.

Keywords

  • hypophosphatasia
  • alkaline phosphatase
  • mineralization
  • bone
  • enzyme replace-ment therapy

1. Introduction

Hypophosphatasia (HPP; Online Mendelian Inheritance in Man (OMIM) #241500,241,510,146,300) is an inherited systemic bone disease that is due to a deficiency of tissue-nonspecific alkaline phosphatase (TNAP) [1, 2, 3]. The first case of HPP was reported by the Canadian pediatrician John Campbell Rathbun in 1948 as a new developmental anomaly [4]. That case was an infantile form, and the patient’s mutations were identified 50 years later using DNA of the surviving parents as a compound heterozygote of p.A114T and p.D294A [5]. Since then, a total of 335 mutations in the gene for TNAP (the ALPL gene) have been reported [6]. The symptoms of HPP vary and are classified into six HPP forms [1, 2]. The pathophysiology of HPP is basically due to a defect of bone mineralization. In severe forms, the patients show skeletal manifestations and respiratory failure derived from costal bone insufficiency, whereas in the mildest forms, they show only dental manifestations [1]. Recent development of enzyme replacement therapy (ERT) has opened up a new vista on the treatment of this previously untreatable disease [7].

2. TNAP: gene, structure of the protein, and its function as an enzyme

There are four human alkaline phosphatase (ALP) isoenzymes (Table 1): TNAP, placental alkaline phosphatase (PLAP), intestinal alkaline phosphatase (IAP), and germ cell ALP [8, 9]. The latter three ALPs are tissue-specific and are expressed in the placenta, intestine, and germ cells (embryonic and cancer cells), respectively [9]. TNAP, also known as the liver/bone/kidney (LBK) alkaline phosphatase, is expressed ubiquitously; liver, bone, kidney, neuronal cells, and white blood cells in particular are tissues that show marked expression [10].

Common nameProtein nameGeneChromosomal locationSites of expressionFunction
Tissue-nonspecific (liver/bone/kidney)TNAP (TNSALP)ALPL1p36.1–34UbiquitousMineralization entrance of pyridoxal phosphate into the neuronal cells
IntestinalIAPALPI2q34–37IntestineDegradation of LPS* lipid absorption
PlacentalPLAP (PAP)ALPP2q34–37PlacentaDegradation of LPS* (?)
Germ cell (placental like)ALPP22q34–37Germ cells
Cancer cells

Table 1.

Isoenzymes of human ALP.

Lipopolysaccharides.


Human TNAP is encoded by the ALPL gene that is located on the short arm of chromosome 1 (1p36.1–34). The coding region of the gene is approximately 1.5 kb in length, and it is extended over more than 50 kb of genomic DNA [11]. The ALPL gene consists of 12 exons of which exons 2–12 are coding exons and there exist two alternative noncoding exons 1 (bone type and liver type) [12, 13]. The promoter region of the gene includes a TATA box, an Sp1 binding site, and a retinoic acid responsive element (RARE) [14, 15]. Retinoic acid regulates the expression of TNAP via RARE [15], whereas another fat-soluble vitamin, active vitamin D (1,25-dihydroxycholecalciferol), regulates the expression of TNAP by modification of the stability of TNAP mRNA [16]. Furthermore, phosphates derived from ALP enzymatic activity are considered to regulate TNAP expression [17]. Epigenetic regulation by methylation of some of the promoter regions of the gene has been reported [18]. However, the precise regulatory mechanism of the ALPL gene regulation, especially its tissue-specific regulation, is not known. On the other hand, the genes encoding tissue-specific ALPs are located on the long arm of chromosome 2 and have a more compact gene structure [19, 20, 21, 22].

The TNAP protein, which has a molecular weight of approximately 80 kDa, is linked to the outer cell membrane through a glycosylphosphatidylinositol (GPI) anchor [9]. The TNAP protein is initially synthesized as a 66 kDa peptide, and then O- and N-glycosides are attached in the endoplasmic reticulum. Eventually, TNAP is localized on the outer membrane of the cells via a GPI anchor [23]. This GPI anchor is added after hydrophobic amino acid residues at the C-terminus are eliminated. The GPI anchor consists of an ethanolamine phosphate, three residues of mannose, a glucosamine, and a phosphatidylinositol [9]. The precise amino acid residue in TNAP to which the GPI anchor is added has not been elucidated, whereas it is known to be an aspartate residue (D484) in PLAP [24, 25]. An active enzyme consists of a dimer and acts as an ectoenzyme. Approximately 58% of the amino acid residues in human TNAP sequences are conserved among mammalian ALPs [26]. On the other hand, approximately 90% of the amino acid residues are conserved among mammalian TNAPs, which allow prediction of missense mutations responsible for HPP [26]. Since the three dimensional structure of TNAP has not been solved, a simulation model based on human PLAP or mouse IAP is used to discuss TNAP structure [27, 28, 29]. The active site of the enzyme comprises a catalytic serine residue (S92 in the human PLAP), two Zn2+-binding sites, and an Mg2+-binding site. Ca2+ is also necessary as a cofactor. The crown domain is characteristic of mammalian ALPs and is considered to interact with extracellular proteins including collagen [30]. There are also isoforms of TNAP itself that depend on the tissue origin. Since these isoforms have different O-linked sugar chains, they show different patterns on the electrophoresis. [9, 31].

The systematic name of ALP is orthophosphoric-monoester phosphohydrolase [alkaline optimum] (EC 3.1.3.1) that hydrolyzes monophosphate esters, and the optimal pH is between 8 and 10 [9]. Inorganic pyrophosphate (PPi) and pyridoxal 5′-phosphate (PLP) are considered to be natural substrates of the enzyme [32]. PPi is an inhibitor of hydroxyapatite formation, which is essential for bone mineralization. PLP is an active vitamin B6 and is necessary in neuronal cells for the biosynthesis of γ-aminobutyric acid (GABA), which acts as an inhibitory neurotransmitter. PLP on the outside of neuronal cells must be dephosphorylated by TNAP at the cell membrane before it can enter the neuronal cells, and it is then be rephosphorylated within the neuronal cells [32, 33]. In laboratory testing, ALP enzymatic activity is usually estimated using p-nitrophenylphosphate as an artificial substrate [9].

3. Molecular process of mineralization and the role of TNAP in mineralization

Biomineralization in hard tissues including bone occurs in a two-step process [34]. Hypertrophic chondrocytes, osteoblasts, and odontocytes in the bone and dental tissues bud matrix vesicles (MVs) from the cell membrane [2, 35]. MVs are 50–200 nm in diameter and are enclosed by a membrane. MVs are a type of extracellular vesicles; however, the difference between MVs and exosomes, which are secreted by cells in the nonmineralized condition, is unclear [36]. TNAP is one of the most abundant proteins on the membrane of an MV [34]. The other proteins that are abundant in MVs are annexins A2, A5, and A6, Ca2+-ATPase, nucleotide pyrophosphatase phosphodiesterase 1 (NPP1), Pit-1 (a sodium-phosphate cotransporter), and PHOSPHO1, all of which have important roles in mineralization [9, 34]. Biologically, mineralization is defined as the deposition of hydroxyapatite (Ca10(PO4)6(OH)2) crystals among the collagen fibers. If this process is insufficient, extracellular spaces are not mineralized, which leads to the formation of an abnormal soft tissue called osteoid tissue. In the first step of the mineralization, hydroxyapatite is formed in an MV. The membrane lipids of the MV provide a source of phosphate; of these lipids, phosphatidylcholine and phosphatidylethanolamine are hydrolyzed by phospholipase C (PLC), yielding phosphocholine (PCho) and phosphoethanolamine (PEA), respectively [37]. Subsequently, PCho and PEA are hydrolyzed by PHOSPHO1, a cytosolic phosphatase abundant in MVs [38]. The phosphate transporter, Pit-1, provides another source of phosphate. On the other hand, calcium is incorporated into MVs via an annexin calcium channel, which consists of annexins A2, A5, and A6 [34, 35]. When the concentration of calcium phosphate rises beyond the solubility of calcium phosphate, hydroxyapatite crystal formation begins. Subsequently, hydroxyapatite crystals penetrate the MV membrane and elongate in the extracellular space [34, 35]. For the elongation of hydroxyapatite, calcium and phosphate should be provided by the extracellular space. Although calcium ions may be abundant in this milieu, phosphate is provided mainly by the TNAP on the MV membrane, which hydrolyzes PPi to yield inorganic phosphate (Pi) [2, 8, 34]. This hydrolysis by TNAP has dual roles; it supplies a source of phosphate for hydroxyapatite formation and degrades an inhibitor of hydroxyapatite formation (PPi). Ultimately, formed hydroxyapatite crystals deposit among collagen fibers, and mineralization is complete (Figure 1). Although the crown domain of TNAP can bind collagen and is suggested to have a role in hydroxyapatite deposition, it has not been elucidated whether TNAP plays a direct role in hydroxyapatite deposition.

Figure 1.

Mineralization process focusing on the matrix vesicle.

Extracellular PPi is formed by NPP1 on the MV membrane by hydrolysis of ATP and also provided by a membrane transporter of PPi, ANKH (the human homolog of ANK, the mouse progressive ankylosis gene product). Therefore, mineralization is regulated by the balance of the activities of these three molecules: TNAP, NPP1, and ANKH [9, 39, 40], Experiments using mice with knockout of these three genes showed that loss of activity of NPP1 or ANKH leads to hypercalcification (ectopic calcification of aorta and/or vertebrae and joints), whereas that of TNAP causes hypomineralization [41].

4. Clinical features of HPP including laboratory tests

HPP is classified into six forms depending on the onset age and the clinical severity (Table 2): perinatal (lethal) form, perinatal benign form, infantile form, childhood form, adult form, and odontohypophosphatasia [3]. The perinatal form occurs in utero and exhibits the most severe manifestations. Patients are stillborn or die during the early postnatal period. They show hypomineralization of the cranial bone and shortened and deformed limbs during gestation, which are easily revealed by ultrasonic examination. The hypomineralization of bones causes a membranous cranium and early craniosynostosis as well as musculoskeletal disorder after birth. The ribs are also hypomineralized, leading to respiratory failure after birth, which often requires respiratory aid. Failure of respiratory management often causes respiratory infections, which are the main cause of death. Epileptic seizures sometimes occur due to a deficit of PLP in neuronal cells, since PLP needs TNAP to enter neuronal cells. A deficit of PLP in neuronal cells causes a decrease in the inhibitory neurotransmitter GABA, leading to epileptic seizures. The perinatal benign form is a recently reported form [42]. Although the symptoms are recognized in gestation, prognosis is good and nonlethal. The infantile form occurs before 6 months of age and also shows severe manifestations. Patients display rickets and deformity of ribs and limbs, and fail to thrive. They also exhibit respiratory failure due to hypomineralization of the ribs, which requires respiratory aid. Recent progress in respiratory management elongates their lifespan. In addition, they often show hypercalcemia and hypercalciuria, leading to nephrocalcinosis. The childhood form shows manifestations after 6 months of age, whose symptoms are milder and not life-threatening. Patients show deformity of limbs, delayed walking, waddling gait, and muscle weakness. Craniosynostosis and high intracranial pressure sometimes occur. These patients also show premature loss of deciduous teeth due to failure of cementum formation [43]. Radiologically, childhood form patients exhibit a characteristic tongue-like radiolucent projection from the rachitic growth plate into the metaphysis due to a focal bone defect at the ends of long bones [1, 3]. The adult form occurs during middle age. Although the natural history of the adult form has not been well characterized, patients sometimes have a history of rickets and/or premature loss of deciduous teeth [44]. In the adult form, osteomalacia develops with pain associated with often recurring metatarsal stress fractures. In some patients, calcium pyrophosphate dehydrate crystals are deposited on articular cartilage due to an increase in concentrations of endogenous PPi [1]. Odontohypophosphatasia manifests only dental symptoms such as premature loss of deciduous teeth without skeletal symptoms due to rickets or osteomalacia.

FormInheritance patternOnsetSymptomsPrognosis
PerinatalARIn uteroDeformity of extremitiesLethal
Membranous cranium
Respiratory failure
Epileptic seizures
Perinatal benignAR or ADIn uteroRicketsBenign
InfantileARAfter birthRickets, CraniosynostosisMostly lethal
Before 6 months of ageRespiratory failure
Failure to thrive
Epileptic seizures
Premature loss of deciduous teeth
ChildhoodAR or ADAfter 6 months of ageRicketsBenign
Musculoskeletal weakness
Premature loss of deciduous teeth
AdultAR or ADMiddle ageOsteomalaciaBenign
Stress fractures
OdontohypophosphatasiaAR or ADPremature loss of deciduous teethBenign
Dental caries

Table 2.

Clinical features of hypophosphatasia.

AR: autosomal recessive, AD: autosomal dominant.

A common histopathological feature of HPP is hypomineralization of bone and teeth [1]. Extracellular hydroxyapatite crystals are reduced, although mineralization occurs within the MV, because PHOSPHO1 acts in the MV. Elongation of hydroxyapatite is impaired. Osteoid tissues are increased in bone, which contains nonmineralized extracellular matrix, and they cause rickets or osteomalacia [45].

For all forms, a characteristic laboratory finding is low serum alkaline phosphatase activity, in which the bone isozyme is reduced [1]. In addition, the natural enzyme substrates, plasma PPi and PLP are elevated. Urine PEA is also elevated, although it is doubtful whether this compound is a natural substrate of TNAP. However, because urine PEA is easy to evaluate by using high-performance liquid chromatography (HPLC), the measurement of PEA is widely used for the diagnosis [2]. The combination of low ALP activity with elevated PPi or PEA is strong evidence for HPP. In some milder cases, however, an increase in PEA is not shown, and, in some cases, PEA is slightly elevated in carriers [46]. Signs and symptoms of HPP are summarized in Table 3.

General
 Failure to thrive
 Poor feeding
 Weakness
Skeletal
 Hypomineralization
 Rickets/osteomalacia
 Short, deformed limbs
 Membranous cranium
 Craniosynostosis
 Deformed ribs
 Skeletal pain
 Short statue
Muscular
 Muscle weakness
 Gait disturbances; delayed walking, waddling gait
Neuronal
 Epileptic seizures (pyridoxine dependent)
 Irritability
Respiratory
 Respiratory failure
Renal
 Nephrocalcinosis
Dental
 Premature loss of deciduous teeth
 Dental caries
Blood examination
 Reduced serum ALP
 Elevated plasma PPi, PLP and PEA
 Elevated plasma Ca2+
Urinalysis
 Elevated urine PEA
 Elevated urine Ca2+

Table 3.

Signs and symptoms of HPP.

Different presentation of symptoms is exhibited depend on the forms.

5. Genetic aspect of HPP

5.1. Inheritance of HPP

HPP is an autosomal recessive inherited disease [1]. Carriers usually do not exhibit any manifestations. Sometimes, however, carriers show subnormal serum ALP activity and slightly higher urine PEA values [2, 46]. The penetrance differs among forms. In some milder cases, an autosomal dominant cases have been reported [47, 48], and the dominant negative effect accounts for some autosomal dominant cases [48]. In addition, different severity of the symptoms within the same family has been reported [49, 50], suggesting the involvement of epigenetic mechanisms.

5.2. Prevalence of HPP

The prevalence of HPP was estimated as 1 in 100,000 live births in the Toronto area in Canada, where the first case was found [51]. In Manitoba, Canada, the prevalence is higher in the Mennonite group, being 1 in 2500, according to a founder effect of a particular mutation [52]. In Europe, the prevalence of severe cases is estimated as 1 in 300,000 [53], whereas in Japan it is 1 in 450,000 for patients who have the c.1559delT allele [46]. This particular allele is a severe allele and is characteristic of Japanese families (46.8% of Japanese patients with HPP have this deletion allele) [46].

5.3. Genetic diagnosis

When HPP is suspected, collection of the family history and the making of a pedigree are important for genetic counseling [54]. Clinical diagnosis can be done by laboratory biochemical examinations and ultrasonic and radiographic findings. Definitive diagnosis is performed by genetic testing. Genomic DNA of the patient is amplified, and the nucleotide sequences are determined. Polymerase chain reaction-single-strand conformation polymorphism (PCR-SSCP), PCR-denaturing gradient gel electrophoresis (PCR-DGGE), and high-resolution melting curve analysis (HRM) methods used to be employed for this purpose, but direct nucleotide sequencing may be the most effective current method of analysis. Once the mutation of the proband is determined, the inheritance can be pursued by testing the parents’ DNA, which makes it possible to give a genetic counseling, because the inheritance pattern of HPP is basically Mendelian inheritance [54, 55]. However, as mentioned above, the same mutation can result in different phenotypes in some families. In addition, a rare case of paternal uniparental isodisomy has been reported [56]. Once a genetic diagnosis is established, enzymatic activity and mineralization activity can be evaluated [57]. An expression plasmid containing the mutant cDNA is transfected into U2OS cells, which are osteoblast-like cells that lack ALP activity. The cells are then cultured for an appropriate period, and enzymatic activity is estimated. For the mineralization assay, the transfected cells are cultured in a mineralization medium that contains β-glycerophosphate as an artificial substrate for TNAP, with or without ascorbic acid. After about 5 days of culture, mineralization is estimated by Alizarin Red S staining [57].

5.4. Prenatal diagnosis

Prenatal diagnosis by ALP enzymatic assay or by immunological detection using amniotic fluid and chorionic villus has been reported, but their diagnostic value is low [3] because of contamination of fetal intestinal ALP and maternal ALP. HPP can be diagnosed using ultrasonography and radiography during the second trimester, but the differential diagnosis is complicated. DNA-based diagnosis using chorionic villus is accurate if information about the nucleotide sequences within the family has been obtained [54, 58]. However, prediction of the prognosis of the disease is not easy, because of the fact that the same mutations can cause different phenotypes even in the same family. In addition, ethical considerations including genetic counseling are very important when prenatal genetic diagnosis is performed [54].

6. Mutations in the ALPL gene

To date, a total of 335 mutations in the ALPL gene have been reported [6]. The TNAP gene mutations’ databases (http://www.sesep.uvsq.fr/03_hypo_mutations.php) of the University of Versailles-Saint Quentin en Yvelines provide up-to-date information regarding mutations [55]. Almost all of these mutations are located within the exons, although some mutations are in the promoter region, exon-intron boundaries and introns. In addition, over 70% of the mutations are missense mutations, 11% are small deletions, 6% are splicing mutations, 5% are nonsense mutations, 3% are small insertions, and 3% are large deletions [6]. Only one regulatory mutation has been reported [59]. Many of the patients are compound heterozygotes. Generally, the interaction between the mutant alleles determines the phenotypes of the patients. Residual activities of mutant TNAPs influence the enzymatic activity and the mineralizing activity of the compound heterozygotes. However, the relationships of genotype and phenotype are rather complicated, and the phenotypes are not always estimated from the combination of the genotypes. Mutation sites are scattered throughout the gene, but there are some “hot spots.” In Caucasian patients, p.E191K (a moderate allele with a dominant negative effect) and p.D378V (a severe allele) are frequent mutations [60, 61], whereas c.1559delT (pL520RfsX86; a severe allele) and p.F327L (a moderate allele) are frequent in Japanese patients [62, 63]. c.1559delT also has founder effects, and the frequency of c.1559delT is mentioned above [46, 62].

7. Structure and function of mutant TNAP

Mutation sites of TNAP proteins are classified by its domain structure [30]. Severe phenotypes are associated with the mutations that are located in the active site and its vicinity, the homodimer interface, the crown domain, and the calcium-binding domain. Mutations in the active site valley (the entry site of the substrate into the active site) resulted in less severe phenotypes [30]. Mutations in the other regions of the protein are inclined to show residual enzymatic activity and are, therefore, milder phenotypes.

Because most of the patients are compound heterozygotes, the residual activity and phenotype are determined by the interaction of two mutant proteins [55]. In some cases, especially in autosomal dominant cases, dominant negative mechanisms are suggested, in which cases the mutant proteins affect the function of the wild-type enzymes [48]. Those interactions have not been precisely elucidated and need to be explored in more detail in order to reveal the genotype–phenotype interrelationships and pathophysiology of HPP.

8. Treatment of HPP based on the pathophysiology of the disease

There have been several trials for the treatment of HPP. Respiratory aid somehow succeeds in saving life in the perinatal and the infantile forms, although it is a symptomatic treatment. Other symptomatic treatments are diet therapies, including calcium restriction and vitamin D supplementation, and surgical operations for bone fractures and craniosynostosis [1]. In terms of treatment based on the pathophysiology of HPP, ERT has been attempted. Whyte et al. used the serum of Paget’s disease patients who exhibited a high level of TNAP for enzyme replacement [64]. Infusion of PLAP has also been attempted based on the observation that, when the patients with mild forms become pregnant, which causes a high serum ALP level according to an increase in PLAP, they sometimes show improvement of symptoms. Those ERT attempts, however, failed to improve the symptoms [3]. Bone marrow transplantation (BMT) and mesenchymal cell transplantation have also been attempted. Those trials showed a slight improvement but an insufficient effect [65]. Successful ERT was reported in 2012, in which bioengineered TNAP was administered [7]. The C-terminal membrane-bound region of human TNAP was eliminated and replaced with the Fc region of human IgG and deca-aspartate sequences [66]. This bioengineered TNAP is, therefore, soluble, can be easily purified using the Fc region, and has high affinity for hydroxyapatite through acidic peptides such as deca-aspartate [66]. Before the trial, an animal experiment using the bioengineered TNAP in a knockout mouse (Akp2−/−; AKP2 is the mouse homolog of the ALPL) that is a good mimic of the perinatal form of HPP, showed elongation of life and improvements in bone and dental defects without respiratory failure [66, 67]. The clinical trial with the bioengineered TNAP (ENB-0040; asfotase alfa) was conducted with five perinatal and six infantile patients [7]. It was administered first as a single intravenous infusion of 2 mg/kg, which was then followed by subcutaneous injections three times per week at a dose of 1 mg/kg for 48 weeks. With the exception of one case who died of respiratory failure that was unrelated with asfotase alfa, the recruited patients showed improvements in rickets and respiratory failure [7]. Asfotase alfa (StrensiqST; Alexion Pharmaceuticals, Inc.) was approved in Japan, the EU, Canada, and the USA in that order in 2015 [2]. Asfotase alfa has dramatically changed the treatment of HPP [68]. Asfotase alfa is indicated for the treatment of patients with perinatal-, infantile- and juvenile-onset HPP [69], in which juvenile-onset HPP means almost the same as the childhood form. The current protocol of the recommended administration is subcutaneous injection six times a week at a dose of 1 mg/kg or three times a week at 2 mg/kg, and the maximal volume of injection is 1 ml [69]. The half-life of asfotase alfa is 5 days in the case of subcutaneous administration. The most common adverse reactions (≥ 10%) are injection site reactions, lipodystrophy, ectopic calcifications, and hypersensitivity reactions. Patients with HPP are at increased risk for developing ectopic calcifications, especially of the eye including the cornea and conjunctiva, and the kidneys (nephrocalcinosis). Although ectopic calcification of the blood vessels has not been reported, it is conceivable that long -term administration may cause medial artery calcification. Medial artery calcification or Mönckeberg-type calcification is often shown as a lethal complication in chronic kidney disease (CKD) patients [70]. In CKD patients, hyperphosphatemia triggers transformation of smooth muscle cells in the media into osteoblastic cells that express elevated TNAP, which then stimulates calcification in the medial artery by a mechanism similar to that of bone mineralization [71, 72]. Asfotase alfa is still not indicated for milder form HPP patients. In this regards, the natural history of the adult form has not been well elucidated [44], and more study is needed. Similarly, odontohypophosphatasia may be still underdiagnosed, because dentists usually do not evaluate the serum ALP value. There should be more investigation into the feasibility of using asfotase alfa for those milder forms.

9. Future perspective

Although current ERT has drastically changed the treatment of HPP, many problems are indicated regarding asfotase alfa administration. First of all, two or three injections per week are needed for this ERT treatment, which burdens patients with injections and parents with administration fees. The interval between injections can be elongated by introducing some modifications into the enzyme preparation. Other possible therapies are bone marrow stem-cell transplantation and/or combination therapy of such transplantation with ERT. Another possible trial is a trial of gene therapy. Using viral vectors, gene therapy was successfully used to treat knockout mice (AKP2−/−) [73, 74]. Since a viral vector containing ALPL cDNA that is injected into blood cannot maintain an effective concentration, gene therapy in combination with stem-cell transplantation (ex vivo gene therapy) may be more effective [75]. Once gene-transferred stem cells are transplanted, no other injection may be necessary [2]. Although gene therapy seems to be a promising procedure, results have so far only been obtained for mouse models, and its feasibility and safety in humans must be investigated.

10. Conclusions

HPP is a systemic skeletal disorder that is caused by TNAP deficiency. Human TNAP is one of the four isoenzymes of alkaline phosphatase and is expressed ubiquitously. The TNAP protein is linked to the outer membrane of cells via a GPI anchor and works as an enzyme in a homodimer state. TNAP is essential for biomineralization; it is located on the MV membrane and plays a role in the elongation of hydroxyapatite crystals into the extracellular space.

HPP is classified into six forms and clinical severity varies among the forms. Hypomineralization of hard tissues is a common feature of HPP. In the severe forms, patients show rickets and respiratory failure that cause death. Milder forms exhibit musculoskeletal disorder or teeth problems. Although low serum ALP activity and an elevated urine PEA value are characteristic of HPP, genetic diagnosis is the definitive diagnosis. ERT using a genetically modified enzyme (asfotase alfa) opens up a new vista in the therapy of HPP, especially for severe forms of HPP. Although asfotase alfa has drastically changed the treatment of HPP, there remain still several problems with its use that need to be resolved.

Conflict of interest

The author has received honoraria from Alexion Pharmaceuticals, Inc. The author reports no other conflict of interest in this work.

© 2017 The Author(s). Licensee IntechOpen. This chapter is distributed under the terms of the Creative Commons Attribution 3.0 License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Hideo Orimo (December 20th 2017). Hypophosphatasia: A Systemic Skeletal Disorder Caused by Alkaline Phosphatase Deficiency, Pathophysiology - Altered Physiological States, David C. Gaze, IntechOpen, DOI: 10.5772/intechopen.70597. Available from:

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