Anthony Jeremy R, Ioachimescu Adriana G
aDivision of Endocrinology, Department of Internal Medicine bDepartment of Neurosurgery, Emory University, Atlanta, Georgia, USA.
Curr Opin Endocrinol Diabetes Obes. 2014 Dec;21(6):476-82. doi: 10.1097/MED.0000000000000109.
To provide an update on current understanding of osteoporosis associated with acromegaly.
Patients with acromegaly have an increased risk of morphometric vertebral fractures. This seems to correlate with acromegaly activity and its duration, but it persists after biochemical control is achieved. Coexistent hypogonadism, diabetes mellitus and over-replacement with glucocorticoids have additional detrimental effects. Bone mineral density can be normal, increased or decreased, and is usually discordant with occurrence of fractures. However, a decrease in the hip bone mineral density during follow-up has been associated with development of new vertebral fractures. Bone turnover markers are increased and tend to normalize after biochemical control of acromegaly. Hypercalcemia rarely occurs in acromegaly and may be parathyroid hormone-dependent or 1,25 dihydroxy-vitamin D dependent. The latter improves with biochemical control of acromegaly.
Screening with thoracic and lumbar vertebral radiographs is indicated in patients with acromegaly. We recommend biochemical control of acromegaly, treatment of hypogonadism and other risk factors of osteoporosis and avoiding supraphysiologic doses of glucocorticoids. Further studies are needed to understand mechanisms of skeletal fragility in acromegaly and clinical impact of vertebral fractures. Further studies of tailored therapy for patients with acromegaly and osteoporosis are also needed.
提供关于肢端肥大症相关骨质疏松症当前认识的最新进展。
肢端肥大症患者发生形态计量学椎体骨折的风险增加。这似乎与肢端肥大症的活动及其持续时间相关,但在生化指标得到控制后仍会持续存在。并存的性腺功能减退、糖尿病以及糖皮质激素替代过量会产生额外的有害影响。骨矿物质密度可正常、升高或降低,且通常与骨折的发生不一致。然而,随访期间髋部骨矿物质密度的降低与新的椎体骨折的发生有关。骨转换标志物升高,在肢端肥大症生化指标得到控制后往往会恢复正常。高钙血症在肢端肥大症中很少见,可能依赖甲状旁腺激素或1,25-二羟维生素D。后者在肢端肥大症生化指标得到控制后会改善。
肢端肥大症患者应进行胸腰椎X线片筛查。我们建议控制肢端肥大症的生化指标,治疗性腺功能减退和骨质疏松症的其他危险因素,并避免使用超生理剂量的糖皮质激素。需要进一步研究以了解肢端肥大症中骨骼脆弱的机制以及椎体骨折的临床影响。还需要对肢端肥大症和骨质疏松症患者的定制治疗进行进一步研究。