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Hypophosphatemic rickets represents a group of heritable renal disorders of phosphate characterized by hypophosphatemia, normal or low serum 1,25 (OH)2 vitamin D and calcium levels. Hypophosphatemia is associated to interglobular dentine and an enlarged pulp chambers.
Our goal was to verify the dental abnormalities and the oral health condition in these patients.
Prospective study of oral conditions in patients with Hypophosphatemic rickets. This report employed a simple method to be easily reproducible: oral clinical exam and radiographic evaluation.
Fourteen patients were studied, 5 males, median age of 11years (4 to 26). Occlusion defects (85,7%) and enamel hypoplasia (57,1%) were significant more frequently than dental abscesses (one patient). We observed enlarged pulp chambers in 43% of the patients and hypoplasia and dentin abnormalities in 14,3%. We could not detect a significant correlation between dental abnormalities and delayed treatment (p>0,05). DMFT index for 6 to 12 years patients (n=12) showed that the oral health is unsatisfactory (mean DMFT= 5).
Patients with Hypophosphatemic Rickets frequently present dental alterations and these are not completely recovered with the treatment, unless dental abscess and they need a periodical oral examination.
Hypophosphatemic rickets represents a group of heritable disorders of phosphate renal regulation with very similar features and with three known forms of inheritance: autosomal dominant (ADHR), autosomal recessive (ARHR) and X‐linked dominant (XLH), with the latter being the most common form. In all three types of hypophosphatemic rickets, an increased FGF23 activity has been demonstrated. FGF‐23 inhibits renal phosphate resorption in the proximal tubule of the kidney by decreasing of the number of sodium‐phosphate cotransporters (NPT2a). It also inhibits 1‐alpha hydroxylase1,2 and, consequently, diminishes the production of 1,25‐(OH)2 vitamin D, thus reducing the intestinal absorption of phosphate and calcium. Patients can present osteomalacia or rickets,3 and the bone abnormalities are frequently restricted to the lower limbs and manifest clinically as pain while walking and skeletal deformities, with frequent genu varum. Inorganic phosphate (Pi) is required for cellular functions and skeletal mineralization, and hypophosphatemia is associated with dysplastic, poorly mineralized dentin with areas of interglobular dentin (hypomineralization), and enlarged pulp chambers.4 Therefore, although the functional properties of odontoblasts are normal, dental and oral abnormalities can occur in these patients and have been observed more frequently in the primary dentition. Recurrent spontaneous abscess formation that affects multiple noncarious primary teeth is the principle clinical finding described in literature.5
Our goal was to verify the dental abnormalities and oral health condition in patients with hypophosphatemic rickets.
We studied 20 patients (aged 0‐18 years at diagnosis) with hypophosphatemic rickets who were followed at the Pediatric Nephrology Unit of Instituto da Criança – Hospital das Clinicas da Faculdade de Medicina da Universidade de São Paulo (HCFMUSP). The patients presented normal renal function (clearance of creatinine ≥90 ml/minute/1.73 m2). Only patients with good compliance were included in the study, and this assessment was based on the results of laboratory exams and adherence to the scheduled visits and exams. Patients with other renal or systemic diseases were excluded from the study.
Clinical evaluations of the patients periodically, every 3 or 4 months, in which the patients were submitted to the following exams: serum phosphate and calcium measurements and intact parathyroid hormone (PTH), alkaline phosphatase and urinary calcium. Renal ultrasonography control was performed annually to check for nephrocalcinosis. Other exams were conducted when necessary. The patients received the conventional treatment based on phosphate and 1,25‐(OH)2 vitamin D supplementation.
Stature was evaluated each attendance, and the mean deviation score (z‐score) for height calculated according to a standard method.6
In this study, we employed a stature z‐score ≤ ‐ 1,9 as a marker of delayed treatment or poor compliance based on previous reports from others and our group demonstrating the correlation between a higher stature z‐score and early and adequate treatment.7,8,9,10
Oral examinations were performed at the Dentistry Division of HC‐FMUSP. For each patient, we performed an anamnesis and an interview consisting of identification data, age, medical history including main complaints, presence of other diseases, familial history and treatment administered, dental history and oral hygiene. The same dentist carried out the oral examinations in all patients to assess the teeth, gingival tissue, mucosa, tongue, and hard and smooth palate.
We adopted the following parameters of the World Health Organization Oral Health Survey Basic Methods to evaluate oral health status:11
The results were compared with the findings obtained for the Brazilian general population.12
The patients were also submitted to a radiological exam (panoramic X‐ray or orthopantomographic X‐ray) that was interpreted by the same radiologist, who evaluated the pulp chamber, root canals, dental abscesses, dental agenesis, dental morphology, dental caries and areas of infection.
Data are presented as the mean ± standard deviation for normally distributed data and as the median and range for non‐normally distributed data. The chi‐square test was used to analyze categorical data, and the correlations were tested using Pearson's correlation coefficients. A p value <0.05 was considered significant.
The Local Ethics Committee approved the protocol.
Fourteen of 20 patients were included in this study: five males and 9 females, aged 4 to 26 years, with a median age of 11 years. Six patients were excluded from the study because they did not fulfill the inclusion criteria for adherence. The diagnosis was established prior to 4 years of age in seven patients (50%). All of the patients were taking phosphate supplementation (20 to 90 mg/kg/day) and calcitriol (0,03 ± 0,01 µg/kg/day), and some of the patients with a tendency to develop hypercalciuria were receiving potassium citrate to prevent nephrocalcinosis or to avoid its progression, with urinary pH control.
At the time of the study, six patients presented with permanent dentition, 6 patients with mixed dentition and 2 patients with deciduous teeth.
The observed tooth abnormalities are shown in Table 1. As can be observed, occlusion defects and enamel hypoplasia were significantly more frequent than dental abscesses.
The occlusion defects included an open bite in four patients, an end‐to‐end rim or occlusion in 2 patients, a cross‐bite in 1 patient, an ogival palate in 1 patient and 4 patients were under orthodontic treatment.
Figure 1 shows the dental clinical of a patient with hypophosphatemic rickets.
Table 2 shows the radiological findings in patients with hypophosphatemic rickets. Enlarged pulp chambers were found in 43% of the patients; however, hypoplasia and dentin abnormalities were also observed.
Figure 2 shows the radiological findings of one patient, emphasizing the enlarged pulp chamber.
We were unable to detect a significant correlation between the presence of dental abnormalities (radiographic abnormalities, hypoplasia and malocclusion) and delayed treatment or poor compliance (stature z‐score ≤ ‐1,9) (p > 0,05).
The oral health status of the patients with primary dentition was insufficient for evaluation, because in the present series, this group comprised only two patients, both of whom presented a dmft index = 0. The DMFT index of the 6 to 12‐year‐old patients (12 patients) showed that oral health in this group was unsatisfactory (mean DMFT= 5) compared to the Brazilian general population (mean DMFT= 1,57).
Inorganic phosphate plays a major role in many biological systems, including cell membrane functions, energy metabolism, cell signaling, and oxygen transport. In hypophosphatemic rickets, renal proximal tubular resorption is compromised, and the patient presents with hypophosphatemia along with a relative 1,25‐(OH)2 vitamin D deficiency. Patients with hypophosphatemic rickets often exhibit high pulp horns, large pulp chambers, and dentinal clefts.
Malocclusion associated with hypophosphatemic rickets has not been frequently reported. However, impressive results were obtained herein (12/14 cases). An open bite was the most frequent abnormality detected and can be explained by the delay in maxillary growth in relation to the growth of the mandible (Angle class II).19 Although taurodontism has been reported in the literature, no cases presented with an abnormality in dental morphology in the present study.20,21
The management of these cases remains controversial. Some authors advocate extraction of the teeth that present periradicular abscesses and eventual restoration with implants. However, endodontic and restorative treatments may not be capable of maintaining asepsis.22,23 Dental abscesses are the most frequently reported complication in the literature.13 Histologically, the teeth exhibit enlarged pulp chambers, wide predentin zone, marked globular dentin and tubular dentin defects that extend from the pulp to the enamel. Enamel hypoplasia may or may not be present.14 Most of the analyzed primary incisors displayed fissures that linked the enamel subsurface to the pulp horn. Abe et al (1988) have suggested that the globular dentin caused by hypophosphatemia impairs calcification.15 The incompletely mineralized dentin exists in the form of calcospherites, which trap microorganisms and impair mechanical endodontic cleaning. These elements may explain the presence of bacteria and dental abscesses. Because enamel and dentin formation occur between 4 months in utero and 11 months of age, defects in the primary dentition usually cannot be prevented. According to Hillmann and Geurtsen,16 the permanent teeth might also be affected by this mechanism, and histopathological examination of the permanent dentition is necessary.
Chaussain‐Miller et al (2007) studied seven patients aged 3 to 16 years and observed that untreated or inadequately treated patients had necrotic teeth with impaired dentin mineralization.17 They concluded that adequate treatment ensures healthy dentin development and mineralization and prevents dental necrosis. This proposition could explain our low rate of dental abscesses, because the patients included is the present study were relatively well treated (50% of the patients started treatment before 4 years of age and appeared to adhere to the treatment).
Typically, the younger the patient when the first abscess appears, the more severe is the dental manifestation.18 However, permanent teeth form after birth, and their development could potentially be improved by the initiation of medication soon after birth.16
The occurrence of spontaneous abscesses following a shallow cavity preparation requires aggressive preventive dental procedures.24 In this sense, professional dental care consisting of periodic examinations, topical fluoride applications and maintenance of good oral hygiene is imperative.25
Pit and fissure sealants are useful when the teeth are erupting, as they prevent the ingress of bacteria into enamel microfractures and the initiation of caries in deep pits and fissures.Few studies have evaluated oral health in patients with hypophosphatemic rickets. Baroncelli et al studied nine children and observed that d/D ranged from 0 to 9 and f/F from 0 to 3. The dfmt index was 0 in the three youngest patients.26 Their findings are similar to ours and demonstrate that oral health in older patients is unsatisfactory compared to that in younger patients and in the healthy population.
In the present study, we evaluated the oral status of patients with hypophosphatemic rickets using a simple, reproducible method: a clinical and radiographic exam. Exams that are more detailed would be useful, but in most situations, such tests are not available. We conclude that patients with hypophosphatemic rickets can frequently present dental abnormalities that are incompletely reversed with treatment. However, early treatment could probably avoid dental abscess formation. Moreover, dentists and pediatricians should be aware of the features of this disorder, because early intervention could prevent subsequent serious and more invasive dental procedures. Patients with hypophosphatemic rickets require periodic oral examinations; the dental care of these patients should consist of topical fluoride applications, pit and fissure sealants and maintenance of good oral hygiene.