Impaired Bone Microarchitecture in Patients with Hereditary Hemochromatosis and Skeletal Complications

• Published in: Calcified tissue international 2020-05, Vol.106 (5), p.465-475
• Main Authors: Jandl, Nico Maximilian, Rolvien, Tim, Schmidt, Tobias, Mussawy, Haider, Nielsen, Peter, Oheim, Ralf, Amling, Michael, Barvencik, Florian
• Format: Article
• Language: English
• Subjects: Biochemistry; Biomedical and Life Sciences; Bone density; Bone diseases; Bone marrow; Bone mineral density; Bone turnover; Cell Biology; Computed tomography; Cortical bone; Dual energy X-ray absorptiometry; Edema; Endocrinology; Ferritin; Fractures; Gonads; Hemochromatosis; Intestine; Iron; Life Sciences; Mineralization; Original Research; Orthopedics; Osteonecrosis; Osteoporosis; Pancreas; Parenchyma; Risk assessment; Risk factors; Transferrins
• ISSN: 0171-967X; 1432-0827
• DOI: 10.1007/s00223-020-00658-7

Hereditary hemochromatosis (HHC) is characterized by excessive intestinal iron absorption resulting in a pathological increase of iron levels. Parenchyma damage may be a consequence of iron deposition in affected organs (e.g., liver, pancreas, gonads) as well as bones and joints, leading to osteoporosis with increased fracture risk and arthropathy. Up to date, it is not known whether HHC can also be considered as a risk factor for osteonecrosis. Likewise, the underlying skeletal changes are unknown regarding, e.g., microstructural properties of bone. We aimed to study the spectrum of skeletal complications in HHC and the possible underlying microarchitectural changes. Therefore, we retrospectively analyzed all patients with HHC ( n  = 10) presenting in our outpatient clinic for bone diseases. In addition to dual-energy X-ray absorptiometry (DXA), high-resolution peripheral quantitative computed tomography (HR-pQCT) was performed and bone turnover markers, 25-OH-D3, ferritin and transferrin saturation were measured. Cortical volumetric bone mineral density (Ct.BMD) and cortical thickness (Ct.Th) were reduced, whereas trabecular microstructure (Tb.Th) and volumetric bone mineral density (Tb.BMD) were preserved compared to age- and gender-adjusted reference values from the literature. Interestingly, the occurrence of bone complications was age dependent; while younger patients presented with osteonecroses or transient bone marrow edema, patients older than 65 years presented with fractures. Our study provides first insights into altered bone microarchitecture in HHC and sheds new light on the occurrence of osteonecrosis. If available, HR-pQCT is a useful complement to fracture risk assessment and to determine microstructural deterioration and volumetric bone mineralization deficits.