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妊娠期间的骨质疏松性椎体骨折:警惕潜在的遗传病因。

Osteoporotic vertebral fractures during pregnancy: be aware of a potential underlying genetic cause.

机构信息

Department of Internal Medicine (N.C.-O., L.O., M.C.Z.), Erasmus MC, 3015 CE Rotterdam, The Netherlands; Department of Human Genetics (L.H.H.), Radboud Medical Center, 6500 HC Nijmegen, The Netherlands; Department of Internal Medicine (R.M.K.), Albert Schweitzer Hospital, 3318 AT Dordrecht, The Netherlands; and Departments of Ophthalmology (C.C.W.K.) and Clinical Genetics (M.E.H.S.), Erasmus MC, 3015 CE Rotterdam, The Netherlands.

出版信息

J Clin Endocrinol Metab. 2014 Apr;99(4):1107-11. doi: 10.1210/jc.2013-3238. Epub 2014 Jan 13.

Abstract

CONTEXT

Although the baby growing in its mother's womb needs calcium for skeletal development, osteoporosis and fractures very rarely occur during pregnancy.

CASE PRESENTATION

A 27-year-old woman in the seventh month of her first pregnancy contracted midthoracic back pain after lifting an object. The pain was attributed to her pregnancy, but it remained postpartum. Her past medical history was uneventful, except for severely reduced vision of her left eye since birth. Family history revealed that her maternal grandmother had postmenopausal osteoporosis and her half-brother had three fractures during childhood after minor trauma. Her height was 1.58 m; she had no blue sclerae or joint hyperlaxity. Laboratory examination including serum calcium, phosphate, alkaline phosphatase, creatinine, β-carboxyterminal cross-linking telopeptide of type I collagen, 25-hydroxyvitamin D, and TSH was normal. Multiple thoracic vertebral fractures were diagnosed on x-ray examination, and dual-energy x-ray absorptiometry scanning showed severe osteoporosis (Z-scores: L2-L4, -5.6 SD; femur neck, -3.9 SD). DNA analyses revealed two compound heterozygous missense mutations in LRP5. The patient's mother carried one of the LRP5 mutations and was diagnosed with osteoporosis. Her half-brother, treated with cabergoline for a microprolactinoma, also had osteoporosis of the lumbar spine on dual-energy x-ray absorptiometry and carried the same LRP5 mutation. The patient was treated with risedronate for 2.5 years. Bone mineral density and back pain improved. She stopped bisphosphonate use 6 months before planning a second pregnancy.

CONCLUSION

Our patient was diagnosed with osteoporosis pseudoglioma syndrome/familial exudative vitreoretinopathy. Potential underlying genetic causes should be considered in pregnancy-associated osteoporosis with implications for patients and relatives. More studies regarding osteoporosis treatment preceding conception are desirable.

摘要

背景

尽管胎儿在母亲子宫中生长时需要钙来进行骨骼发育,但妊娠期间很少发生骨质疏松症和骨折。

病例介绍

一位 27 岁的初产妇,在妊娠第七个月时,提重物后出现中胸背部疼痛。疼痛归因于妊娠,但产后仍持续存在。她既往无特殊病史,仅左眼视力自出生以来严重下降。家族史显示,其外祖母患有绝经后骨质疏松症,同父异母的弟弟在童年时因轻微外伤发生了 3 次骨折。她的身高为 1.58 m,无巩膜蓝色变或关节过度松弛。实验室检查包括血清钙、磷、碱性磷酸酶、肌酐、I 型胶原羧基端交联肽、25-羟维生素 D 和 TSH,均正常。X 线检查诊断为多发性胸椎骨折,双能 X 线吸收仪扫描显示严重骨质疏松症(Z 评分:L2-L4,-5.6 SD;股骨颈,-3.9 SD)。DNA 分析显示 LRP5 存在两个复合杂合错义突变。该患者的母亲携带其中一个 LRP5 突变,被诊断为骨质疏松症。其同父异母的弟弟因微催乳素瘤接受卡麦角林治疗,双能 X 线吸收仪也显示腰椎骨质疏松症,携带相同的 LRP5 突变。该患者接受利塞膦酸钠治疗 2.5 年。骨密度和背痛均改善。她在计划第二次妊娠前 6 个月停止使用双膦酸盐。

结论

该患者诊断为骨质疏松假瘤综合征/家族性渗出性玻璃体视网膜病变。对于与妊娠相关的骨质疏松症,应考虑潜在的遗传原因,这对患者及其亲属均有影响。在受孕前进行骨质疏松症治疗的相关研究更有必要。

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