Diagnosis |
Key Points |
DXA Recommendations |
Celiac Disease |
- Celiac disease is a risk factor for low BMD secondary to malabsorption
- Children with concomitant autoimmune endocrinopathy (type 1 diabetes, Addison’s disease, etc.) may be at higher risk of impaired bone health2
- Strict adherence to a gluten-free diet typically results in resolution of low bone density
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- There is no strong evidence for routine DXA scans at baseline or follow-up
- Consider DXA 1-2 yrs after diagnosis or when anti-TTG antibody normalizes.
|
Cystic Fibrosis |
- Children with cystic fibrosis are at increased risk of low BMD due to malnutrition, steroid use, and concurrent disease (cirrhosis, short bowel syndrome, celiac disease)3
- Children without concurrent disease or malnutrition are at low risk for low BMD
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|
Inflammatory Bowel Disease |
- Inflammation from IBD has an adverse effect on bone modeling and the muscle-bone unit
- Chronic steroid use also increases the risk of low bone density
- Low bone density often resolves with control of inflammation related to disease treatment4
|
- Consider baseline at diagnosis
- Repeat as needed with risk factors:
- Persistent malnutrition
- Short stature
- Significant glucocorticoid therapy
- Amenorrhea
- Delayed puberty
- Persistent inflammation
- Increased CRP, ESR, or low albumin
- Clinically significant fractures
- Repeat every 1-2 yrs for height-adjusted Z-score < -1
|
Diagnosis |
Key Points |
DXA Recommendations |
Chemotherapy for Childhood Cancer |
- Children treated with methotrexate and/or steroids are at increased risk for low BMD
- Children who have undergone a hematopoietic cell transplant are at risk for low BMD5
|
- Baseline DXA by 18 yrs old or 2 yrs after the end of chemotherapy
- Screening DXA for high-risk children:
- Severe disease
- Low body weight
- Chronic glucocorticoid therapy
- Delayed puberty
- Gonadal failure
- History of fracture
|
Hematopoietic Cell Transplant (HSCT) |
Children who have undergone a hematopoietic cell transplant are at risk for low BMD9 |
Annual DXA screening and monitoring should be considered before and 12 mos after HSCT |
Sickle Cell Anemia |
Sickle cell leads to a significantly reduced BMD compared with healthy subjects |
Screening DXA, follow up as clinically indicated |
Thalassemia |
Children with thalassemia have lower BMD than healthy children and suboptimal peak bone mass |
Consider DXA and follow up as indicated based on Z-score |
Diagnosis |
Key Points |
DXA Recommendations |
Duchenne’s Muscular Dystrophy |
- DMD is associated with low BMD and increased fracture rates, especially in the setting of glucocorticoids6
|
- Annual lateral spine radiograph for vertebral fracture recommended in all children on steroids
- Annual DXA starting at age 5 yrs; frequency can be spaced to every 2-3 yrs in ambulatory males with Z-scores > 0
|
Ketogenic Diet |
Children on long-term ketogenic diet at risk for impaired bone accrual, as well as abnormalities in calcium metabolism7 |
- Screening DXA in all children after 2 yrs on ketogenic diet
- Follow-up frequency as indicated based on Z-score and other clinical risk factors
|
Neurodevelopmental Disorders (Autism, Rett Syndrome, etc) |
Children with autism and Rett syndrome at risk for low bone density d/t limited physical activity, restricted dietary intake8, 9 |
- Indications for screening DXA in children with autism unclear; consider in children with fracture, limited activity or impaired dietary intake
- Baseline DXA after age 5 recommended in all children with Rett syndrome
- Follow-up frequency for both conditions as indicated based on Z-score, other clinical risk factors
|
Neuromuscular Weakness (Cerebral Palsy, Spinal Muscular Atrophy, Spinal Cord Injury, etc.) |
Children with neuromuscular disorders of any type have increased fracture rates and reduced DXA BMD Z-scores due to muscle weakness and immobilization10 |
- Indications for screening DXA unclear; consider in high-risk children:
- Fracture
- Quadriplegia
- Limited ambulation
- Previous fracture
- Anticonvulsant use
- Low body weight/BMI
- Follow-up frequency as indicated based on Z-score, other clinical risk factors
|
Diagnosis |
Key Points |
DXA Recommendations |
Eating Disorders |
- Defined as female adolescent with excessive exercise or
> 6 mos of amenorrhea
- Imbalance of the gonadal sex hormones increases the risk of low BMD
|
- Indications for screening unclear; consider screening DXA in children with duration of illness 9-12 mos, fracture
- Follow-up frequency as indicated based upon Z-score, other clinical factors
|
Gender Dysphoria/Transgender Health |
- The treatment of gender dysphoria in youth includes the use of gonadotropin releasing hormone analogs that may impair bone mineral accrual
- Children with delayed onset or inconsistent sex steroid hormone administration may be at greater risk12
|
- Indications for screening and monitoring with DXA are emerging
- Current recommendations suggest monitoring DXA every
1-2 yrs in children on puberty blockers
- Z-scores should be reported respective to both assigned and affirmed gender
|
Steroid Exposure |
Chronic high dose steroid use decreases bone density and increases fracture risk |
- Consider screening DXA in children on chronic therapy for 90 days of hydrocortisone, prednisone/prednisolone, or dexamethasone at doses that exceed physiological replacement
-
Chronic Steroid Use
- Follow-up frequency as indicated based upon Z-score, other clinical factors
|