The Faculty of Education, Health and Wellbeing, University of Wolverhampton, Gorway Rd, Walsall, WS1 3BD, UK.
Centre of Research, Education, Innovation and Intervention in Sport, Faculty of Sports, University of Porto, Porto, Portugal.
Osteoporos Int. 2018 Oct;29(10):2261-2274. doi: 10.1007/s00198-018-4610-x. Epub 2018 Jul 5.
The association of genetic polymorphisms with low bone mineral density in elite athletes have not been considered previously. The present study found that bone mass phenotypes in elite and pre-elite dancers are related to genetic variants at the Wnt/β-catenin and ER pathways.
Some athletes (e.g. gymnasts, dancers, swimmers) are at increased risk for low bone mineral density (BMD) which, if untreated, can lead to osteoporosis. To investigate the association of genetic polymorphisms in the oestrogen receptor (ER) and the Wnt/β-catenin signalling pathways with low BMD in elite and pre-elite dancers (impact sport athletes).
The study included three phases: (1) 151 elite and pre-elite dancers were screened for the presence of low BMD and traditional osteoporosis risk factors (low body weight, menstrual disturbances, low energy availability); (2) a genetic association study was conducted in 151 elite and pre-elite dancers and age- and sex- controls; (3) serum sclerostin was measured in 101 pre-elite dancers and age- and sex-matched controls within a 3-year period.
Eighty dancers revealed low BMD: 56.3% had at least one traditional osteoporosis risk factor, whereas 28.6% did not display any risk factor (37.2% revealed traditional osteoporosis risk factors, but had normal BMD). Body weight, menstrual disturbances and energy availability did not fully predict bone mass acquisition. Instead, genetic polymorphisms in the ER and Wnt/β-catenin pathways were found to be risk factors for low BMD in elite dancers. Sclerostin was significantly increased in dancers compared to controls during the 3-year follow-up (p < 0.05).
Elite and pre-elite dancers demonstrate high prevalence of low BMD, which is likely related to genetic variants at the Wnt/β-catenin and ER pathways and not to factors usually associated with BMD in athletes (body weight, menstrual disturbances, energy deficiency).
以前没有考虑过遗传多态性与精英运动员低骨密度之间的关系。本研究发现,精英和准精英舞者的骨量表型与 Wnt/β-catenin 和 ER 通路的遗传变异有关。
一些运动员(如体操运动员、舞蹈演员、游泳运动员)患低骨密度(BMD)的风险增加,如果不治疗,可能导致骨质疏松症。为了研究雌激素受体(ER)和 Wnt/β-catenin 信号通路中的遗传多态性与精英和准精英舞者(冲击运动运动员)低 BMD 的关系。
该研究包括三个阶段:(1)筛查 151 名精英和准精英舞者是否存在低 BMD 和传统骨质疏松症危险因素(低体重、月经紊乱、能量供应不足);(2)在 151 名精英和准精英舞者以及年龄和性别匹配的对照组中进行遗传关联研究;(3)在 3 年内,测量 101 名准精英舞者和年龄、性别匹配的对照组的血清硬化素。
80 名舞者的 BMD 较低:56.3%至少有一个传统骨质疏松症危险因素,而 28.6%没有任何危险因素(37.2%有传统骨质疏松症危险因素,但 BMD 正常)。体重、月经紊乱和能量供应并不能完全预测骨量的获得。相反,ER 和 Wnt/β-catenin 通路中的遗传多态性被发现是精英舞者低 BMD 的危险因素。在 3 年的随访中,舞者的硬化素明显高于对照组(p<0.05)。
精英和准精英舞者的低 BMD 患病率较高,这可能与 Wnt/β-catenin 和 ER 通路的遗传变异有关,而与运动员通常与 BMD 相关的因素(体重、月经紊乱、能量缺乏)无关。