Wang Lulu, Wang Qian, Sun Junyan, Huang Yuanxin, Zhang Qiuwan, Wei Liutong, Yin Shengju, Lai Dongmei
The International Peace Maternity and Child Health Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Shanghai Key Laboratory of Embryo Original Diseases, Shanghai, China.
Hum Reprod. 2025 Jan 3. doi: 10.1093/humrep/deae297.
Is elevated plasma molybdenum level associated with increased risk for idiopathic premature ovarian insufficiency (POI)?
Elevated plasma molybdenum level is associated with an increased risk of idiopathic POI through vascular endothelial injury and inhibition of granulosa cell proliferation.
Excessive molybdenum exposure has been associated with ovarian oxidative stress in animals but its role in the development of POI remains unknown.
STUDY DESIGN, SIZE, DURATION: Case-control study of 30 women with idiopathic POI and 31 controls enrolled from August 2018 to May 2019. In vitro experimentation. Animal studies using distilled water containing sodium molybdate.
PARTICIPANTS/MATERIALS, SETTING, METHODS: Logistic regression analysis of the association between plasma concentrations of molybdenum and calcium and POI odds ratio. Plasma samples were from 30 patients with idiopathic POI and 31 controls. Both groups were comparable in terms of age and body mass index. Proliferation assay, flow cytometry analyses for cell cycle, nitric oxide and calcium, gene expression, and protein analysis using human umbilical vein endothelial cells and KGN (human ovarian granulosa-like tumor cell line) cells. Sexual hormones, ovarian function, vascular injury, and platelet activation were evaluated in mice exposed to excessive molybdenum.
Case-control study showed that the elevation of plasma concentrations of molybdenum and calcium was positively associated with the POI odds ratio. In vitro study showed that molybdenum treatment increased the permeability of human umbilical vein endothelial cells through enhancing nitric oxide generation and cytosolic calcium influx. In vivo study showed that increased vascular permeability induced by molybdenum resulted in platelet activation and serotonin release within mouse ovaries. Serotonin decreased granulosa cell proliferation by inducing cellular quiescence. Molybdenum also directly inhibited granulosa cell proliferation by downregulating isocitrate dehydrogenase (IDH1). Inhibition of granulosa cell proliferation ultimately led to ovarian dysfunction in mice, including altered estrus cycles, serum sex hormone concentrations, ovarian morphology, and ovarian reserve.
LIMITATIONS, REASONS FOR CAUTION: There are two limitations in the current study. First, it remains unclear whether the elevation of plasma molybdenum content is due to environmental exposure or altered metabolism. Second, rigorous and multicenter studies, with a larger sample size, should be carried out to confirm the elevation of plasma molybdenum and calcium concentrations in patients with idiopathic POI.
Our findings highlight an association between elevated plasma concentrations of molybdenum and calcium and increased risk of idiopathic POI. This discovery offers crucial insights into the pathogenesis of idiopathic POI and the search for effective preventive measures.
STUDY FUNDING/COMPETING INTEREST(S): This work was supported by the National Natural Science Foundation of China (82271664), the interdisciplinary program of Shanghai Jiao Tong University (YG2022ZD028), the Research Projects of Shanghai Municipal Health Committee (202240343), and Shanghai Clinical Research Center for Cell Therapy (23J41900100). None of the authors has any conflict of interest to disclose.
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血浆钼水平升高是否与特发性卵巢早衰(POI)风险增加有关?
血浆钼水平升高与特发性POI风险增加有关,其机制是通过血管内皮损伤和抑制颗粒细胞增殖。
在动物中,过量的钼暴露与卵巢氧化应激有关,但其在POI发生发展中的作用尚不清楚。
研究设计、规模、持续时间:2018年8月至2019年5月开展的病例对照研究,纳入30例特发性POI女性和31例对照。体外实验。使用含钼酸钠的蒸馏水进行动物研究。
研究对象/材料、地点、方法:对钼和钙的血浆浓度与POI比值比之间的关联进行逻辑回归分析。血浆样本来自30例特发性POI患者和31例对照。两组在年龄和体重指数方面具有可比性。使用人脐静脉内皮细胞和KGN(人卵巢颗粒样肿瘤细胞系)细胞进行增殖试验、细胞周期的流式细胞术分析、一氧化氮和钙分析、基因表达分析以及蛋白质分析。对暴露于过量钼的小鼠的性激素、卵巢功能、血管损伤和血小板活化进行评估。
病例对照研究表明,钼和钙的血浆浓度升高与POI比值比呈正相关。体外研究表明,钼处理通过增强一氧化氮生成和胞质钙内流增加人脐静脉内皮细胞的通透性。体内研究表明,钼诱导的血管通透性增加导致小鼠卵巢内血小板活化和5-羟色胺释放。5-羟色胺通过诱导细胞静止减少颗粒细胞增殖。钼还通过下调异柠檬酸脱氢酶(IDH1)直接抑制颗粒细胞增殖。颗粒细胞增殖的抑制最终导致小鼠卵巢功能障碍,包括发情周期改变、血清性激素浓度改变、卵巢形态改变和卵巢储备改变。
局限性、注意事项:本研究有两个局限性。第一,尚不清楚血浆钼含量升高是由于环境暴露还是代谢改变。第二,应开展更严格的多中心研究,纳入更大样本量,以确认特发性POI患者血浆钼和钙浓度升高。
我们的研究结果突出了血浆钼和钙浓度升高与特发性POI风险增加之间的关联。这一发现为特发性POI的发病机制及寻找有效的预防措施提供了关键见解。
研究资金/利益冲突:本研究得到中国国家自然科学基金(82271664)、上海交通大学交叉学科项目(YG2022ZD028)、上海市卫生健康委员会科研项目(202240343)以及上海细胞治疗工程技术研究中心(23J41900100)的支持。作者均无利益冲突需披露。
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