Authors

1 Associate Professor of Pediatric Hematology and Oncology, Mashhad University of Medical Sciences, Mashhad, Iran.

2 Associate Professor of Pediatric Endocrine and Metabolism, Mashhad University of Medical Sciences, Mashhad, Iran.

3 Resident of Pediatrics, Mashhad University of Medical Sciences, Mashhad, Iran.

Abstract

Introduction: 
Acute Lymphoblastic Leukemia (ALL) is the most common malignancy in children and the main form of childhood leukemia (75%). ALL different treatment options have a great impact on children weight and appetite. The improving prognosis for children with cancer refocuses attention to long-term outcomes with an emphasis on quality of life. More survival rate allows researchers to evaluate long term complication of ALL and its different treatment options such as endocrine abnormalities for example decreased bone mineral density.
METHODS: 
a systematic web base search was conducted in MEDLINE up to December 2014.
We included articles with available abstract in English language, and participants younger than 18 years. Manual searching was done within the reference list of articles.  Two reviewers independently reviewed and assessed eligibility criteria, assessed quality, and extracted data.
RESULTS: 
Trace elements concentration decline due to malabsorption or inadequate intake in children with ALL. Osteopenia occurs more frequent in younger children and those who treated with higher doses of corticosteroids.
CONCLUSION: 
The dietary history of ALL patients who are at more risk for fractures and osteopenia should be screened by paying more attention to calcium and vitamin D intake.

Keywords

Introduction

Despite recent scientific progress, etiology of childhood Leukemia is still unknown. It is a multifactorial condition in which genetic and environment have important role (1). Chromosome translocation frequent occurrence is confirming for leukemia genetic base. Patients with Down syndrome, Ataxia Telangiectasia and Wiscott Aldrich syndrome would be at more risk for developing leukemia. Leukemia is more common in children who have siblings with malignancy (2). Its risk increases in twins. Some of environmental factor which are associated with leukemia are: Ionizing radiation, some bacterial and viral infections and chemotherapy and alkaline agents. Alcohol and smoking habits might relate to ALL. Its prevalence is slightly higher in white race. Male gender is a prognostic factor for ALL. ALL peak age is between 2 and 5 years (2, 3).

Annually, 2500 to 3500 leukemia cases have been diagnosed in the United States of America (4). Its incidence is 40 in each one million children younger than 15 years. Acute lymphoblastic leukemia (ALL) is the main form of childhood leukemia (75%). Chronic forms of are very rare in childhood. Neoplastic diseases are the main second cause of childhood death in all around world. Lymphoid leukemia incidence has been increased 1% per year in recent two decades (5).

ALL survival rate has been improved regard to new inventions in radiotherapy technology and chemotherapy agents. And also supporting care services and patients close follow up lead to increase survival rate from zero in 1950 to 80% in recent years (6). More survival rate allows researchers to evaluate long term complication of ALL and its different treatment options. One of the most important categories of these complications is endocrine abnormalities which include hypothyroidism, metabolic syndrome and insulin resistance growth retardation, decreased bone mineral density and growth hormone (GH) deficiency (7). 

ALL different treatment options have a great impact on children weight and appetite. A nutrition status has a great impact on ALL prognoses. Malnutrition influence growth indexes in children such as weight, height and arm circumference. It has been confirmed that children whose weight and height are two SD lower than normal have poor prognoses. And malnutrition causes intolerance to chemotherapy (8).  This study was designed to assess bone mass density in childhood ALL and the efficacy of calcium and vitamin D supplement.

Method, search strategy and Data sources

Articles were selected by searching the Cochrane Library and MEDLINE up to December 2014. Our key word and Medical Subject Headings (MESH) were broad terms such as "acute lymphoblastic leukemia" AND "bone mass density" AND "calcium" AND "vitamin D". Retrieved articles were assessed to identify additional related articles from their reference list. We included articles with available abstract, full text in English language. Manual searching was conducted within the reference list of articles. 

Critical appraisal

Firstly, abstracts were reviewed by two independent researchers. So, 32 abstracts were screened for relevancy two times. 17 were excluded due to no relevancy. The remaining 15 abstracts were fully assessed by our two reviewers.  Regard to article type, 2 case reports and 2 reviews were excluded from further evaluation.   

We used consort quality appraisal from to assess the quality of selected studies.

Two reviewers independently scored the quality criteria for each included study and a third reviewer resolved any discrepancies. We used a structural data extraction tool. But due to heterogeneity in hormone and outcome measurements, a Meta analysis was not performed. The flow diagram of literature search is shown in Figure-1.

 

 

Results

The oldest study was published in 1995 and the most recent one in 2014. Table-1 shows the general characteristics of the included studies. 1335 children with ALL was evaluated in these 14 studies. Three study were randomized controlled trials, and other 11 ones were cohort studies.

Table-1: Summary of the 15 studies included in the review

Reference NO.

year

target  population

Sample size

design

Final result

9

2014

Male children

215

cohort

ALL treatments did not increase bone turnover.

6

2014

children

275

RCT

ALL treatments lead to bone turnover.

10

2012

children

50

cohort

ALL treatments lead to bone turnover.

11

2012

children

18

cohort

ALL treatments lead to bone turnover.

12

2012

children

164

cohort

ALL treatments lead to bone turnover.

13

2010

children

70

cohort

85% of the ALL patients had bone mineralization defect.

14

2008

children

110

RCT

ALL treatments lead to bone turnover.

15

2008

children

200

RCT

ALL treatments lead to bone turnover.

16

2005

children

10

cohort

ALL treatments lead to bone turnover.

17

2004

children

59

cohort

ALL treatments did not increase bone turnover.

18

1999

children

28

cohort

ALL treatments lead to bone turnover.

19

1998

children

56

cohort

 

ALL treatments lead to bone turnover.

20

1996

children

40

cohort

 

ALL treatments lead to bone turnover.

21

1995

children

40

cohort

 

ALL treatments lead to bone turnover.

 

 

Discussion

Trace elements concentration might decline due to malabsorption or inadequate intake in children with ALL. On the other hand long term hospital stay and immobility and corticosteroid therapy in ALL patients lead to osteopenia and bone loss. It seems that osteopenia and osteonecrosis are more common in ALL and Non-Hodgkin lymphoma (NHL). And it happens in one third of these patients. Osteopenia occurs more frequent in younger children and those who treated with higher doses of corticosteroids. Osteopenia in these patients is bilateral and multi articular in weight bearing part like hip (22). In some ALL patients osteoporosis is the only manifestation the underlying malignancy (3).

Vitamin D is a crucial factor for body systems which is involved in the metabolism of tissues. Its main classic role is bone metabolism regulation and calcium homeostasis. Vitamin D deficiency might lead to rickets in children. Vitamin D level is lower in people with darker skin type, in autumn and winter and places which are located in higher latitudes. Malnutrition, increase in vitamin D exertion amount impaired vitamin D activation and resistance to 1, 25 (OH) 2 D biologic effects are some causes of vitamin D insufficiency (23).

Recently the number of reports has been increased about metabolic and endocrine abnormalities in adults who had ALL and NHL in childhood. Endocrine disorder and reduction in to insulin sensitivity is happen in 20 to 50 percent of these patients. Growth retardation, body mass index (BMI) abnormalities, thyroid and puberty disorders in these children influence bone mineral density. Corticosteroid administration, cytotoxic drugs and radiotherapy down regulate bone metabolism (24).

Choi showed that treatment with glucocorticoid and lower BMI are the main factors associated with osteopenia in children with malignancies. Z-score of -1 to -2 is more common in female patients with a history of cranial radiotherapy (25).  Gunes revealed that 85% of the survivors of childhood ALL had bone mineralization defect in adolescence. BMD and bone indexes reduce significantly during the first treatment years. Low daily calcium intake is the main cause of this problem, so prophylactic calcium and vitamin D supplement administration might be helpful in these cases. Although cholecalciferol and calcium supplementation added benefit had not been confirmed in all adult survivors of ALL (26).  

It seems that bone turnover in this population is associated with age, tanner stage, gender and BMI. And bone turnover could not be used to predict LS-BMD Z-score (27). Some studies revealed that children who suffer from ALL and have lower bone mineral density of the lumbar spine are at more risk for fractures. Pamidronate is safe and effective in children with low BMD during and after chemotherapy (28).

The majority of intervention studies with dairy foods or calcium supplement in children and adolescents from different ethnic backgrounds have shown positive effects on bone mineral accretion at one or more of the sites measured (7, 23).

High-dose methotrexate (HD-MTX) administration in children is associated with long-term side effects on bone metabolism and leads to insufficiency fractures and osteopenia (28).

We proposed that the dietary history of children who are at more risk for fractures and osteopenia should be screened by paying more attention to calcium and vitamin D intake.

Conclusion

The dietary history of children who are at more risk for fractures and osteopenia should be screened by paying more attention to calcium and vitamin D intake.

Conflict of interests: None.

Acknowledgment

The authors are grateful to all colleagues for their help during the study period.

 

  1.  

    1. Zhu K1, Prince RL. Calcium and bone. Clin Biochem. 2012 Aug;45(12):936-42. doi: 10.1016/j.clinbiochem.2012.05.006. Epub 2012 May 17.
    2. Blijdorp K1, van Waas Mvan der Lely AJPieters Rvan den Heuvel-Eibrink MNeggers S. Endocrine sequelae and metabolic syndrome in adult long-term survivors of childhood acute myeloid leukemia. Leuk Res. 2013 Apr;37(4):367-71. doi: 10.1016/j.leukres.2012.12.008. Epub 2013 Jan 9.
    3. Choi YJ1, Park SYCho WKLee JWCho KSPark SH. Factors related to decreased bone mineral density in childhood cancer survivors. J Korean Med Sci. 2013 Nov;28(11):1632-8. doi: 10.3346/jkms.2013.28.11.1632. Epub 2013 Oct 31.
    4. Gurney JG1, Kaste SCLiu WSrivastava DKChemaitilly WNess KK. Bone mineral density among long-term survivors of childhood acute lymphoblastic leukemia: results from the St. Jude Lifetime Cohort Study. Pediatr Blood Cancer. 2014 Jul;61(7):1270-6. doi: 10.1002/pbc.25010. Epub 2014 Feb 28.
    5. Karakaya P1, Yılmaz S2, Tüfekçi O2, Kır M3, Böber E4, Irken G2, Oren H2. Endocrinological and cardiological late effects among survivors of childhood acutelymphoblastic leukemia. Turk J Haematol. 2013 Sep;30(3):290-9. doi: 10.4274/Tjh.2012.0094. Epub 2013 Sep 5.
    6. Kaste SC1, Qi ASmith KSurprise HLovorn EBoyett J. Calcium and cholecalciferol supplementation provides no added benefit to nutritional counseling to improve bone mineral density in survivors of childhood acute lymphoblastic leukemia (ALL). Pediatr Blood Cancer. 2014 May;61(5):885-93. doi: 10.1002/pbc.24882. Epub 2014 Jan 7.
    7. Lee JMKim JEBae SHHah JO. Efficacy of pamidronate in children with low bone mineral density during and after chemotherapy for acute lymphoblastic leukemia and non-Hodgkin lymphoma. Blood Res. 2013 Jun;48(2):99-106. doi: 10.5045/br.2013.48.2.99. Epub 2013 Jun 25.
    8. Mäkitie OHeikkinen RToiviainen-Salo SHenriksson MPuukko-Viertomies LRJahnukainen K. Long-term skeletal consequences of childhood acute lymphoblastic leukemia in adult males: a cohort study. Eur J Endocrinol. 2013 Jan 17;168(2):281-8. doi: 10.1530/EJE-12-0702. Print 2013 Feb.
    9. Watsky MACarbone LDAn QCheng CLovorn EAHudson MM. Bone turnover in long-term survivors of childhood acute lymphoblastic leukemia. Pediatr Blood Cancer. 2014 Aug;61(8):1451-6. doi: 10.1002/pbc.25025. Epub 2014 Mar 20.
    10. Mostoufi-Moab SBrodsky JIsaacoff EJTsampalieros AGinsberg JPZemel BShults J,Leonard MB. Longitudinal assessment of bone density and structure in childhood survivors of acute lymphoblastic leukemia without cranial radiation. J Clin Endocrinol Metab. 2012 Oct;97(10):3584-92. doi: 10.1210/jc.2012-2393. Epub 2012 Aug 3.
    11. Frisk PArvidson JLjunggren OGustafsson J. Decreased bone mineral density in young adults treated with SCT in childhood: the role of 25-hydroxyvitamin D. Bone Marrow Transplant. 2012 May;47(5):657-62. doi: 10.1038/bmt.2011.147. Epub 2011 Jul 18.
    12. Tylavsky FASmith KSurprise HGarland SYan XMcCammon E. Nutritional intake of long-term survivors of childhood acute lymphoblastic leukemia: evidence for bone health interventional opportunities. Pediatr Blood Cancer. 2010 Dec 15;55(7):1362-9. doi: 10.1002/pbc.22737.
    13. Gunes AMCan ESaglam HIlçöl YOBaytan B. Assessment of bone mineral density and risk factors in childrencompleting treatment for acute lymphoblastic leukemia. J Pediatr Hematol Oncol. 2010 Apr;32(3):e102-7. doi: 10.1097/MPH.0b013e3181d32199.

     14. Rai SNHudson MMMcCammon ECarbone LTylavsky FSmith K et al. Implementing an intervention to improve bone mineral density in survivors of childhood acute lymphoblastic leukemia: BONEII, a prospective placebo-controlled double-blind randomized interventional longitudinal study design.

    15. Díaz PRNeira LCFischer SGTeresa Torres MCMilinarsky ATGiadrosich VR et al. Effect of 1,25(OH)2-vitamin D on bone mass in children with acute lymphoblastic leukemia. J Pediatr Hematol Oncol. 2008 Jan;30(1):15-9. doi: 10.1097/MPH.0b013e318159a522.

    16. Wiernikowski JTBarr RDWebber CGuo CYWright MAtkinson SA. Alendronate for steroid-induced osteopenia in children with acute lymphoblastic leukaemia or non-Hodgkin's lymphoma: results of a pilot study. J Oncol Pharm Pract. 2005 Jun;11(2):51-6.

     17. Muszyńska-Rosłan KKonstantynowicz JKrawczuk-Rybak MŁuczyński WKaczmarski M, Wołczynski S et al. [Bone mineral density and markers of bone turnover in patients treated for malignant disease in childhood]. Med Wieku Rozwoj. 2004 Oct-Dec;8(4 Pt 2):1041-54.

    18. Arikoski PKomulainen JRiikonen PVoutilainen RKnip MKröger H. Alterations in bone turnover and impaired development of bonemineral density in newly diagnosed children with cancer: a 1-year prospective study. J Clin Endocrinol Metab. 1999 Sep;84(9):3174-81.

    19. Atkinson SAHalton JMBradley CWu BBarr RD. Bone and mineral abnormalities in childhood acute lymphoblastic leukemia: influence of disease, drugs and nutrition. Int J Cancer Suppl. 1998;11:35-9.

    20. Halton JMAtkinson SAFraher LWebber CGill GJDawson SBarr RD. Altered mineral metabolism and bone mass in children during treatment for acute lymphoblastic leukemia. J Bone Miner Res. 1996 Nov;11(11):1774-83.

    21. Halton JM1, Atkinson SAFraher LWebber CECockshott WPTam CBarr RD. Mineral homeostasis and bone mass at diagnosis in children withacute lymphoblastic leukemia. J Pediatr. 1995 Apr;126(4):557-64.

    22. Mehlman CT1, Shepherd MANorris CSMcCourt JB. Diagnosis and treatment of osteopenic fractures in children. Curr Osteoporos Rep. 2012 Dec;10(4):317-21. doi: 10.1007/s11914-012-0126-z.

    23. Pirker-Frühauf UM1, Friesenbichler JUrban ECObermayer-Pietsch BLeithner A. Osteoporosis in children and young adults: a late effect after chemotherapy for bone sarcoma. Clin Orthop Relat Res. 2012 Oct;470(10):2874-85. doi: 10.1007/s11999-012-2448-7. Epub 2012 Jul 18.

    24. Rajendran R1, Abu EFadl AByrne CD. Late effects of childhood cancer treatment: severe hypertriglyceridaemia, central obesity, non alcoholic fatty liver disease and diabetes as complications of childhood total body irradiation. Diabet Med. 2013 Aug;30(8):e239-42. doi: 10.1111/dme.12234.

    25. Salim H1, Ariawati KSuryawan WBArimbawa M. Osteoporosis resulting from acute lymphoblastic leukemia in a 7-year-old boy: a case report. J Med Case Rep. 2014 May 28;8:168. doi: 10.1186/1752-1947-8-168.

    26. Szadek LL1, Scharer K2. Identification, Prevention, and Treatment of Children with Decreased Bone Mineral Density. J Pediatr Nurs. 2013 Nov 19. pii: S0882-5963(13)00316-3. doi: 10.1016/j.pedn.2013.11.002. [Epub ahead of print]

    27. te Winkel MLPieters RHop WCRoos JCBökkerink JPLeeuw JA. Bone mineral density at diagnosis determines fracture rate in children with acute lymphoblastic leukemia treated according to the DCOG-ALL9 protocol. Bone. 2014 Feb;59:223-8. doi: 10.1016/j.bone.2013.11.017. Epub 2013 Nov 25.

    28. von Scheven E1, Corbin KJStefano SCimaz R. Glucocorticoid-Associated Osteoporosis in Chronic Inflammatory Diseases: Epidemiology, Mechanisms, Diagnosis, and Treatment. Curr Osteoporos Rep. 2014 Jul 8. [Epub ahead of print]