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Mandibular radiomorphometric assessment of bone mineral density in survivors of pediatric hematopoietic stem-cell transplantation

Abstract

OBJECTIVE:

Hematopoietic stem-cell transplantation (HSCT) childhood survivors of hematologic malignancies are prone to develop late osteopenia and osteoporosis. The purpose of this retrospective study was to quantitatively and qualitatively assess bone mineral density (BMD) in HSCT childhood survivors and to compare the effectiveness of both qualitative and quantitative assessment methods.

METHODS:

DESIGN BMD assessment using panoramic radiographs of childhood HSCT survivors aged 3.69-18.88 years using two radiomorphometric indexes. Case-control double-blinded comparison of panoramic radiographic images from childhood HSCT survivors and age- and sex-matched healthy controls. Quantitative assessment was performed by measuring the cortical bone width bilaterally at the mental foramen level. Qualitative assessment was performed using the mandibular cortical index bilaterally on all panoramic images.

RESULTS:

Radiographs were taken 6.59-83.95 months after bone marrow transplantation [median±SD=25.92±24.9 months]. Fifty-two panoramic radiographic images were analyzed: 21 from HSCT survivors and 31 from healthy controls aged 3.69-25.1 years [mean±SD=11.89±5.28 years]. The mandibular cortical bone width was 17% smaller in childhood HSCT survivors than in healthy controls (case group: 2.420, control group: 3.307; p=0.00617). Qualitative analysis revealed an increased frequency of severe mandibular cortical erosion in childhood HSCT survivors, although no significant difference was observed (case group: 1.540, control group: 1.490; p=0.32). The interobserver agreement was 85% (Kappa index).

CONCLUSIONS:

HSCT childhood survivors exhibit quantitative and qualitative mandibular bone impairments. Further studies are needed to establish an association between mandibular cortical bone impairment and osteoporosis.

Bone Marrow Transplantation; Hematopoietic Stem Cell Transplantation; Children; Osteoporosis; Radiomorphometric Assessment


INTRODUCTION

Hematopoietic stem-cell transplantation (HSCT) plays an important role in the curative management of hematologic high-risk pediatric malignancies, with high rates of long-term disease-free survival (11. Chow EJ, Anderson L, Baker KS, Bhatia S, Guilcher GM, Huang JT, et al. Late Effects Surveillance Recommendations among Survivors of Childhood Hematopoietic Cell Transplantation: A Children’s Oncology Group Report. Biol Blood Marrow Transplant. 2016;22(5):782-95, https://doi.org/10.1016/j.bbmt.2016.01.023.
https://doi.org/10.1016/j.bbmt.2016.01.0...
,22. Ward E, DeSantis C, Robbins A, Kohler B, Jemal A. Childhood and adolescent cancer statistics, 2014. CA Cancer J Clin. 2014;64(2):83-103, https://doi.org/10.3322/caac.21219.
https://doi.org/10.3322/caac.21219...
). Childhood HSCT survivors may be substantially affected by a wide range of adverse late effects, including reduced bone mineral density (BMD) and increased risk of bone fractures, which negatively impact their overall quality of life (33. Pundole X, Cheema HI, Petitto GS, Lopez-Olivo MA, Suarez-Almazor ME, Lu H. Prevention and treatment of bone loss and fractures in patients undergoing a hematopoietic stem cell transplant: a systematic review and meta-analysis. Bone Marrow Transplant. 2017;52(5):663-70, https://doi.org/10.1038/bmt.2016.312.
https://doi.org/10.1038/bmt.2016.312...

4. Le Meignen M, Auquier P, Barlogis V, Sirvent N, Contet A, Simeoni MC, et al. Bone mineral density in adult survivors of childhood acute leukemia: impact of hematopoietic stem cell transplantation and other treatment modalities. Blood. 2011;118(6):1481-9, https://doi.org/10.1182/blood-2011-01-332866.
https://doi.org/10.1182/blood-2011-01-33...
-55. Wilson CL, Ness KK. Bone mineral density deficits and fractures in survivors of childhood cancer. Curr Osteoporos Rep. 2013;11(4):329-37, https://doi.org/10.1007/s11914-013-0165-0.
https://doi.org/10.1007/s11914-013-0165-...
).

Dual-energy X-ray absorptiometry (DXA) of long bones or vertebrae is the preferred method for the diagnosis of low BMD. Despite its high cost, DXA is well established as the gold standard examination for diagnosing osteopenia/osteoporosis, as recommended by the World Health Organization (WHO) (66. Ghassemi A, Banihashem A, Ghaemi N, Elmi S, Erfani Sayyar R, Elmi S, et al. Evaluation of Bone Mineral Density in Children with Acute Lymphoblastic Leukemia (ALL) and Non-Hodgkin’s Lymphoma (NHL): Chemotherapy with/without Radiotherapy. Int J Hematol Oncol Stem Cell Res. 2016;10(3):153-60.).

Morphometric evaluation of panoramic jaw radiographs has been proposed as an alternative to DXA for the screening, diagnosis, and evaluation of low BMD (77. Nagi R, Devi BKY, Rakesh N, Reddy SS, Santana N, Shetty N. Relationship between femur bone mineral density, body mass index and dental panoramic mandibular cortical width in diagnosis of elderly postmenopausal women with osteoporosis. J Clin Diagn Res. 2014;8(8):ZC36-40, https://doi.org/10.7860/JCDR/2014/9210.4748.
https://doi.org/10.7860/JCDR/2014/9210.4...
,88. Al-Dam A, Blake F, Atac A, Amling M, Blessmann M, Assaf A, et al. Mandibular cortical shape index in non-standardised panoramic radiographs for identifying patients with osteoporosis as defined by the German Osteology Organization. J Craniomaxillofac Surg. 2013;41(7):e165-9, https://doi.org/10.1016/j.jcms.2012.11.044.
https://doi.org/10.1016/j.jcms.2012.11.0...
). The qualitative and quantitative assessment of mandibular cortical bone provides predictive information for the early diagnosis of osteoporosis in adults (99. Muramatsu C, Horiba K, Hayashi T, Fukui T, Hara T, Katsumata A, et al. Quantitative assessment of mandibular cortical erosion on dental panoramic radiographs for screening osteoporosis. Int J Comput Assist Radiol Surg. 2016;11(11):2021-32, https://doi.org/10.1007/s11548-016-1438-8.
https://doi.org/10.1007/s11548-016-1438-...

10. Taguchi A, Suei Y, Sanada M, Ohtsuka M, Nakamoto T, Sumida H, et al. Validation of dental panoramic radiography measures for identifying postmenopausal women with spinal osteoporosis. AJR Am J Roentgenol. 2004;183(6):1755-60, https://doi.org/10.2214/ajr.183.6.01831755.
https://doi.org/10.2214/ajr.183.6.018317...

11. Klemetti E, Kolmakov S, Kroger H. Pantomography in assessment of the osteoporosis risk group. Scand J Dent Res. 1994;102(1):68-72, https://doi.org/10.1111/j.1600-0722.1994.tb01156.x.
https://doi.org/10.1111/j.1600-0722.1994...
-1212. Pallagatti S, Parnami P, Sheikh S, Gupta D. Efficacy of Panoramic Radiography in the Detection of Osteoporosis in Post-Menopausal Women When Compared to Dual Energy X-Ray Absorptiometry. Open Dent J. 2017;11:350-9, https://doi.org/10.2174/1874210601711010350.
https://doi.org/10.2174/1874210601711010...
), but few studies have been conducted in children (1313. Allen B, Migliorati C, Rowland C, An Q, Shintaku W, Donaldson M, et al. Comparison of mandibular cortical thickness and QCT-derived bone mineral density (BMD) in survivors of childhood acute lymphoblastic leukemia: a retrospective study. Int J Paediatr Dent. 2016;26(5):330-5, https://doi.org/10.1111/ipd.12203.
https://doi.org/10.1111/ipd.12203...
).

We hypothesized that childhood HSCT survivors have reduced BMD compared to that of healthy control individuals. Using panoramic radiographs, this study aimed to assess bone health quantitatively and qualitatively in childhood HSCT survivors and in age- and gender-matched controls and to compare the effectiveness of both qualitative and quantitative assessment methods.

METHODS

This study was approved by the Research Ethics Committee of the University of São Paulo Medical School (CEP/CONEP number 1.034.483/2015). The case (HSCT) group consisted of digital panoramic radiographic images from childhood HSCT survivors aged 3.69 to 18.88 years who were recruited at the Pediatric Oncology Institute, University of São Paulo Medical School (ITACI-ICR/FM USP), São Paulo, Brazil. The inclusion criteria were as follows: (1) HSCT for the treatment of hematological malignancies; (2) age at time of HSCT ≤18 years; and (3) panoramic radiograph taken at least six months after HSCT.

Information including medical history, birth date, gender, location, age at cancer diagnosis, age at HSCT, and myeloablative conditioning regimen was collected from medical records. Information about the primary malignancy diagnosis was obtained from primary caretakers, and the dental history was retrieved from dental records at the Dental Clinic of the Children’s Institute at the University of São Paulo Medical School.

Panoramic radiographs were taken by the same operator at the Radiology Institute (InRad) of the University of São Paulo Medical School using the same X-ray panoramic machine (Orthophos CD, Siemens, Bensheim, Germany) with imaging settings of 60-90 kVp, 9-12 mAs, and 12 s of exposure. All radiographic images were downloaded with 256 gray levels, 3188×1709 pixels, and 300 dpi resolution in digital format (JPEG) compatible with ImageJ (1.50c4 for Mac OS Sierra 10.12.6, available at https://imagej.nih.gov/ij/).

The control group (CONTROL) consisted of age- and gender-matched healthy subjects selected from a databank at the Dentistry School of the São Paulo State University in São José dos Campos (UNESP-SJC), São Paulo. The exclusion criteria were as follows: (1) early medical complications or previously diagnosed developmental skeletal disorders; (2) previous orthodontic treatment; and (3) history of craniofacial trauma. All participants’ parents or legal guardians provided written consent for their children to participate in the study and were free to withdraw their participation at any time.

Quantitative Assessment

Quantitative analyses of panoramic images were performed using ImageJ (1.50c4 for Mac OS Sierra 10.12.6). The morphometric analysis of radiographic images was performed using well-established radiographic assessment methods proposed by Taguchi et al. (2004) (1010. Taguchi A, Suei Y, Sanada M, Ohtsuka M, Nakamoto T, Sumida H, et al. Validation of dental panoramic radiography measures for identifying postmenopausal women with spinal osteoporosis. AJR Am J Roentgenol. 2004;183(6):1755-60, https://doi.org/10.2214/ajr.183.6.01831755.
https://doi.org/10.2214/ajr.183.6.018317...
). The images were analyzed independently by two blinded researchers, an experienced oral radiologist and an oral and maxillofacial surgeon with 10 years of experience. The images were viewed using the same computer monitor in a quiet, dimly lit room.

The mandibular cortex width was measured bilaterally at the mental foramen level using lines parallel to both the external and internal cortical laminae of the mandibular basal line (Alpha and Beta, respectively). Perpendicular to these lines, an intersecting line was drawn diametrically dividing the mental foramen (Gamma). The distance between the two parallel lines at the intersection with the perpendicular line (ECO) was considered the cortical width of the mandibular inferior border (Figure 1).

Figure 1
Mandibular cortical width as proposed by Taguchi et al. (2004) (10). Alpha: external lamina of the mandibular basal line; Beta: internal lamina of the mandibular basal line; Gamma: perpendicular intersection at the mental foramen level. ECO: bone width of the inferior mandibular cortex.

Qualitative Assessment

The width of the inferior mandibular cortex measured bilaterally in the premolar region in both groups was analyzed by two experienced blinded observers, and interobserver agreement was calculated using the Kappa index. The images were viewed separately by each observer using the same computer monitor in a quiet, dimly lit room.

Panoramic radiographic images were categorized according to the Klemetti index (99. Muramatsu C, Horiba K, Hayashi T, Fukui T, Hara T, Katsumata A, et al. Quantitative assessment of mandibular cortical erosion on dental panoramic radiographs for screening osteoporosis. Int J Comput Assist Radiol Surg. 2016;11(11):2021-32, https://doi.org/10.1007/s11548-016-1438-8.
https://doi.org/10.1007/s11548-016-1438-...
,1111. Klemetti E, Kolmakov S, Kroger H. Pantomography in assessment of the osteoporosis risk group. Scand J Dent Res. 1994;102(1):68-72, https://doi.org/10.1111/j.1600-0722.1994.tb01156.x.
https://doi.org/10.1111/j.1600-0722.1994...

12. Pallagatti S, Parnami P, Sheikh S, Gupta D. Efficacy of Panoramic Radiography in the Detection of Osteoporosis in Post-Menopausal Women When Compared to Dual Energy X-Ray Absorptiometry. Open Dent J. 2017;11:350-9, https://doi.org/10.2174/1874210601711010350.
https://doi.org/10.2174/1874210601711010...

13. Allen B, Migliorati C, Rowland C, An Q, Shintaku W, Donaldson M, et al. Comparison of mandibular cortical thickness and QCT-derived bone mineral density (BMD) in survivors of childhood acute lymphoblastic leukemia: a retrospective study. Int J Paediatr Dent. 2016;26(5):330-5, https://doi.org/10.1111/ipd.12203.
https://doi.org/10.1111/ipd.12203...
-1414. Halling A, Persson GR, Berglund J, Johansson O, Renvert S. Comparison between the Klemetti index and heel DXA BMD measurements in the diagnosis of reduced skeletal bone mineral density in the elderly. Osteoporos Int. 2005;16(8):999-1003, https://doi.org/10.1007/s00198-004-1796-x.
https://doi.org/10.1007/s00198-004-1796-...
15. Weilbaecher KN. Mechanisms of osteoporosis after hematopoietic cell transplantation. Biol Blood Marrow Transplant. 2000;6(2A):165-74, https://doi.org/10.1016/S1083-8791(00)70039-5.
https://doi.org/10.1016/S1083-8791(00)70...
16. Pfeilschifter J, Diel IJ. Osteoporosis due to cancer treatment: pathogenesis and management. J Clin Oncol. 2000;18(7):1570-93, https://doi.org/10.1200/JCO.2000.18.7.1570.
https://doi.org/10.1200/JCO.2000.18.7.15...
17. Mandel K, Atkinson S, Barr RD, Pencharz P. Skeletal morbidity in childhood acute lymphoblastic leukemia. J Clin Oncol. 2004;22(7):1215-21, https://doi.org/10.1200/JCO.2004.04.199.
https://doi.org/10.1200/JCO.2004.04.199...
) as shown briefly in Table 1.

Table 1
Klemetti index categories for panoramic radiographs.

Statistical Analysis

The hypothesis of quantitative mandibular bone changes in childhood HSCT survivors compared with age- and gender-matched healthy controls was tested using the paired t-test in Excel for Mac (Microsoft version 15.37).

The hypothesis of qualitative mandibular bone alterations was tested using the chi-square test in Excel for Mac (Microsoft version 15.37). All other qualitative or categorical variables were described as frequencies and proportions.

RESULTS

Patients and treatment characteristics

Fifty-two panoramic radiographic images were analyzed: 21 from childhood HSCT survivors (14 males and 7 females) and 31 from healthy controls (16 males and 15 females). Participant ages ranged from 3.69 to 25.1 years [mean age±SD=11.89±5.28 years], and there was no significant difference in mean age between cases and controls (p=0.88). The age distribution of both groups is shown in Table 2.

Table 2
Age (years) distribution of childhood HSCT patients and matched controls.

The primary malignancy diagnosis was acute myeloid leukemia (56%), acute lymphoblastic leukemia (38%), and myelodysplastic syndrome (6%). The HSCT type was autogenous in 29% of patients, allogenic in 58% of patients, and umbilical cord in 21% of cases. Myeloablative conditioning was achieved by individualized drug schemes associated with total body radiotherapy in 75% of cases. Cyclophosphamide was administered in 75% of cases in association with other drugs (Figure 2).

Figure 2
Myeloablative chemotherapy drug distribution. CYCLO: cyclophosphamide; MTX: methotrexate; CYTA: cytarabine; MEL: melphalan; BU: busulphan; ETO: etoposide.
Figure 3
Qualitative assessment of mandibular cortical bone erosion in childhood HSCT patients and healthy controls by the Klemetti index (%).

Radiographic images from the HSCT patients were obtained 6.59-83.95 months after bone marrow transplantation [median±SD=25.92±24.9 months] between September 2015 and December 2017.

Quantitative Analyses

The interobserver agreement of quantitative analyses was 85%. The mandibular cortical bone width was 17% smaller in HSCT patients than in healthy controls (case group: 2.420, control group: 3.307; p=0.00617). Dispersion analyses indicated a narrower distribution in the case group (minimum: 1.028; maximum: 3.498; median: 2.605).

Qualitative Analyses

The interobserver agreement of the qualitative analyses was 85%. The qualitative analysis revealed a higher prevalence of severe cortical erosion in the case group, though no statistical significance was found (case group: 1.540, control group: 1.490; p=0.32) (Figure 3).

DISCUSSION

This study shows that compared to age- and gender-matched healthy controls, childhood HSCT survivors (3.69-18.88 years old) of hematologic malignancies have both quantitative and qualitative mandibular cortical bone impairments. These results agree with previous investigations that show that reduced BMD is significantly associated with survivor rates (11. Chow EJ, Anderson L, Baker KS, Bhatia S, Guilcher GM, Huang JT, et al. Late Effects Surveillance Recommendations among Survivors of Childhood Hematopoietic Cell Transplantation: A Children’s Oncology Group Report. Biol Blood Marrow Transplant. 2016;22(5):782-95, https://doi.org/10.1016/j.bbmt.2016.01.023.
https://doi.org/10.1016/j.bbmt.2016.01.0...
,22. Ward E, DeSantis C, Robbins A, Kohler B, Jemal A. Childhood and adolescent cancer statistics, 2014. CA Cancer J Clin. 2014;64(2):83-103, https://doi.org/10.3322/caac.21219.
https://doi.org/10.3322/caac.21219...
).

Quantitative bone changes in these patients are often described in terms of femoral and lumbar bone deficits and reduced BMD (44. Le Meignen M, Auquier P, Barlogis V, Sirvent N, Contet A, Simeoni MC, et al. Bone mineral density in adult survivors of childhood acute leukemia: impact of hematopoietic stem cell transplantation and other treatment modalities. Blood. 2011;118(6):1481-9, https://doi.org/10.1182/blood-2011-01-332866.
https://doi.org/10.1182/blood-2011-01-33...
). HSCT involves corticosteroid administration, which inhibits multiple pathways, including reduced osteoblastic activity, increased osteoclastic bone resorption, and inhibition of vitamin D 1α-hydroxylation with impairment of intestinal calcium absorption and reduced muscle strength (1818. Kang MJ, Lim JS. Bone mineral density deficits in childhood cancer survivors: Pathophysiology, prevalence, screening, and management. Korean J Pediatr. 2013;56(2):60-7, https://doi.org/10.3345/kjp.2013.56.2.60.
https://doi.org/10.3345/kjp.2013.56.2.60...
). Additionally, endocrine complications due to chemotherapy and/or radiotherapy, such as growth hormone deficiency and hypogonadism, can adversely affect BMD (1919. Cho WK, Ahn MB, Lee JW, Chung NG, Jung MH, Cho B, et al. Low bone mineral density in adolescents with leukemia after hematopoietic stem cell transplantation: prolonged steroid therapy for GvHD and endocrinopathy after hematopoietic stem cell transplantation might be major concerns? Bone Marrow Transplant. 2017;52(1):144-6, https://doi.org/10.1038/bmt.2016.199.
https://doi.org/10.1038/bmt.2016.199...
).

The qualitative skeletal changes in young adult survivors of childhood HSCT are associated with an increased risk of bone fractures (1313. Allen B, Migliorati C, Rowland C, An Q, Shintaku W, Donaldson M, et al. Comparison of mandibular cortical thickness and QCT-derived bone mineral density (BMD) in survivors of childhood acute lymphoblastic leukemia: a retrospective study. Int J Paediatr Dent. 2016;26(5):330-5, https://doi.org/10.1111/ipd.12203.
https://doi.org/10.1111/ipd.12203...
,2020. Lin JN, Chen HJ, Yang CH, Lai CH, Lin HH, Chang CS, et al. Risk of osteoporosis and pathologic fractures in cancer patients who underwent hematopoietic stem cell transplantation: a nationwide retrospective cohort study. Oncotarget. 2017;8(21):34811-9, https://doi.org/10.18632/oncotarget.16746.
https://doi.org/10.18632/oncotarget.1674...
). In a large-scale study, Pundole et al. (2015) reported that HSCT recipients were approximately 7-9 times more likely to develop fractures than the general population in the United States (2121. Pundole XN, Barbo AG, Lin H, Champlin RE, Lu H. Increased incidence of fractures in recipients of hematopoietic stem-cell transplantation. J Clin Oncol. 2015;33(12):1364-70, https://doi.org/10.1200/JCO.2014.57.8195.
https://doi.org/10.1200/JCO.2014.57.8195...
). Although bone maturation during puberty increases BMD, children exposed to chemotherapy early in life show reduced BMD at older ages (33. Pundole X, Cheema HI, Petitto GS, Lopez-Olivo MA, Suarez-Almazor ME, Lu H. Prevention and treatment of bone loss and fractures in patients undergoing a hematopoietic stem cell transplant: a systematic review and meta-analysis. Bone Marrow Transplant. 2017;52(5):663-70, https://doi.org/10.1038/bmt.2016.312.
https://doi.org/10.1038/bmt.2016.312...
). The increased risk of fractures negatively impacts quality of life and may ultimately result in extended periods of intensive level medical care and, potentially, life-sustaining treatment modalities (2222. Zenlea IS, Melvin P, Huh SY, Mehta N, Reidy SJ, Rhodes ET, et al. Risk Factors for Fractures in Children Hospitalized in Intensive and Intermediate Care Units. Hosp Pediatr. 2017;7(7):395-402, https://doi.org/10.1542/hpeds.2016-0213.
https://doi.org/10.1542/hpeds.2016-0213...
).

The quantitative and qualitative evaluation methods for BMD impairment used in this study are well-documented techniques that enable the classification of radiographic changes in the mandibular cortex in a cost-effective and highly reproducible manner. Mandibular cortical width has been shown to be positively associated with BMD (1010. Taguchi A, Suei Y, Sanada M, Ohtsuka M, Nakamoto T, Sumida H, et al. Validation of dental panoramic radiography measures for identifying postmenopausal women with spinal osteoporosis. AJR Am J Roentgenol. 2004;183(6):1755-60, https://doi.org/10.2214/ajr.183.6.01831755.
https://doi.org/10.2214/ajr.183.6.018317...
). The Klemetti index is a well-established screening method for reduced skeletal BMD in adults and elderlies (1212. Pallagatti S, Parnami P, Sheikh S, Gupta D. Efficacy of Panoramic Radiography in the Detection of Osteoporosis in Post-Menopausal Women When Compared to Dual Energy X-Ray Absorptiometry. Open Dent J. 2017;11:350-9, https://doi.org/10.2174/1874210601711010350.
https://doi.org/10.2174/1874210601711010...
,1414. Halling A, Persson GR, Berglund J, Johansson O, Renvert S. Comparison between the Klemetti index and heel DXA BMD measurements in the diagnosis of reduced skeletal bone mineral density in the elderly. Osteoporos Int. 2005;16(8):999-1003, https://doi.org/10.1007/s00198-004-1796-x.
https://doi.org/10.1007/s00198-004-1796-...
,2323. Gomes CC, de Rezende Barbosa GL, Bello RP, Boscolo FN, de Almeida SM. A comparison of the mandibular index on panoramic and cross-sectional images from CBCT exams from osteoporosis risk group. Osteoporos Int. 2014;25(7):1885-90.). However, Allen et al. (2016) found no association between qualitative changes in the mandibular cortex and BMD deficits in children and young adult survivors of acute lymphoblastic leukemia (ALL) (1313. Allen B, Migliorati C, Rowland C, An Q, Shintaku W, Donaldson M, et al. Comparison of mandibular cortical thickness and QCT-derived bone mineral density (BMD) in survivors of childhood acute lymphoblastic leukemia: a retrospective study. Int J Paediatr Dent. 2016;26(5):330-5, https://doi.org/10.1111/ipd.12203.
https://doi.org/10.1111/ipd.12203...
).

The current study supports previous research showing that dentists are able to identify patients at risk of low BMD based on mandibular cortical erosion on panoramic radiographs and refer such patients to further exams (1010. Taguchi A, Suei Y, Sanada M, Ohtsuka M, Nakamoto T, Sumida H, et al. Validation of dental panoramic radiography measures for identifying postmenopausal women with spinal osteoporosis. AJR Am J Roentgenol. 2004;183(6):1755-60, https://doi.org/10.2214/ajr.183.6.01831755.
https://doi.org/10.2214/ajr.183.6.018317...
,2323. Gomes CC, de Rezende Barbosa GL, Bello RP, Boscolo FN, de Almeida SM. A comparison of the mandibular index on panoramic and cross-sectional images from CBCT exams from osteoporosis risk group. Osteoporos Int. 2014;25(7):1885-90.). Dental practitioners are part of the healthcare team and can actively help in the early diagnosis of low BMD. Panoramic radiographs are a routine part of the dental evaluation by general dentists, orthodontists, and oral and maxillofacial surgeons; they are a low-cost, easy to perform, standardized exam that exposes patients to low doses of ionizing radiation (2424. Kadesjo N, Lynds R, Nilsson M, Shi XQ. Radiation dose from X-ray examinations of impacted canines: cone beam CT vs two-dimensional imaging. Dentomaxillofac Radiol. 2018;47(3):20170305, https://doi.org/10.1259/dmfr.20170305.
https://doi.org/10.1259/dmfr.20170305...
) and could serve as a screening tool to prevent late effects of HSCT in adult life through highly sensitive exams that can ultimately help improve multidisciplinary care and quality of life (2525. Zinter MS, Holubkov R, Steurer MA, Dvorak CC, Duncan CN, Sapru A, et al. Pediatric Hematopoietic Cell Transplant Patients Who Survive Critical Illness Frequently Have Significant but Recoverable Decline in Functional Status. Biol Blood Marrow Transplant. 2018;24(2):330-6, https://doi.org/10.1016/j.bbmt.2017.10.036.
https://doi.org/10.1016/j.bbmt.2017.10.0...
).

One methodological limitation of the present study was the absence of more extensive follow-up of childhood HSCT survivors. The study population was recruited at the Pediatric Oncology Institute of the University of São Paulo Medical School, a public tertiary reference center for multiple regional public health care units that provides diagnosis for more complicated cases frequently associated with higher recurrence and lower survival rates. In this scenario, antineoplastic regimens for myeloablative purposes are highly tailored with multiple drug schemes and precise dose adjustments, resulting in nonhomogeneous study groups.

In summary, compared to healthy individuals, childhood HSCT survivors exhibit significant quantitative changes in mandibular cortex width with an increased risk of fractures. Further studies are needed to assess the risk of osteoporosis in childhood HSCT survivors.

CLINICAL IMPLICATIONS

  • - This paper identifies a deficit where oral healthcare providers could improve the overall health in children after HSCT.

  • - This paper demonstrates that the Klemetti technique is not a predictor of BMD in this population but that Taguchi’s evaluation method could be used as a screening protocol.

  • - Childhood HSCT survivors are a population at risk for reduced BMD, and close follow-up is needed.

AUTHOR CONTRIBUTIONS

Frascino AV and Costa C conceived the ideas. Fava M and Salgado DMRA collected the data. Coracin FL analyzed the data. Odone-Filho V led the writing of this manuscript.

ACKNOWLEDGMENTS

We thank Dr. Terezinha Sampaio Amaral and the InRad medical team for their help and support.

REFERENCES

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    Chow EJ, Anderson L, Baker KS, Bhatia S, Guilcher GM, Huang JT, et al. Late Effects Surveillance Recommendations among Survivors of Childhood Hematopoietic Cell Transplantation: A Children’s Oncology Group Report. Biol Blood Marrow Transplant. 2016;22(5):782-95, https://doi.org/10.1016/j.bbmt.2016.01.023
    » https://doi.org/10.1016/j.bbmt.2016.01.023
  • 2
    Ward E, DeSantis C, Robbins A, Kohler B, Jemal A. Childhood and adolescent cancer statistics, 2014. CA Cancer J Clin. 2014;64(2):83-103, https://doi.org/10.3322/caac.21219
    » https://doi.org/10.3322/caac.21219
  • 3
    Pundole X, Cheema HI, Petitto GS, Lopez-Olivo MA, Suarez-Almazor ME, Lu H. Prevention and treatment of bone loss and fractures in patients undergoing a hematopoietic stem cell transplant: a systematic review and meta-analysis. Bone Marrow Transplant. 2017;52(5):663-70, https://doi.org/10.1038/bmt.2016.312
    » https://doi.org/10.1038/bmt.2016.312
  • 4
    Le Meignen M, Auquier P, Barlogis V, Sirvent N, Contet A, Simeoni MC, et al. Bone mineral density in adult survivors of childhood acute leukemia: impact of hematopoietic stem cell transplantation and other treatment modalities. Blood. 2011;118(6):1481-9, https://doi.org/10.1182/blood-2011-01-332866
    » https://doi.org/10.1182/blood-2011-01-332866
  • 5
    Wilson CL, Ness KK. Bone mineral density deficits and fractures in survivors of childhood cancer. Curr Osteoporos Rep. 2013;11(4):329-37, https://doi.org/10.1007/s11914-013-0165-0
    » https://doi.org/10.1007/s11914-013-0165-0
  • 6
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Publication Dates

  • Publication in this collection
    30 May 2019
  • Date of issue
    2019

History

  • Received
    2 Sept 2018
  • Accepted
    27 Feb 2019
Creative Common - by 4.0
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