目的研究血清中25(OH)D水平对隐匿型原发性卵巢功能不全(occult primary ovarian insufficiency,oPOI)患者妊娠结局的影响。方法回顾性分析2018年9月至2022年12月在广东省妇幼保健院生殖中心行辅助生殖治疗的218例患者的临床资料。将符...目的研究血清中25(OH)D水平对隐匿型原发性卵巢功能不全(occult primary ovarian insufficiency,oPOI)患者妊娠结局的影响。方法回顾性分析2018年9月至2022年12月在广东省妇幼保健院生殖中心行辅助生殖治疗的218例患者的临床资料。将符合纳入标准的对照组和oPOI组患者按孕产妇的年龄节点分为≤35岁和>35岁,比较各组的25(OH)D浓度及妊娠结局的差异,随后对oPOI患者进行维生素D补充,追踪助孕结局。结果在≤35岁患者中,oPOI组的25(OH)D水平及妊娠率显著低于对照组(41.62±11.90 vs 63.04±16.26,42.37±4.62 vs 53.33±1.97,P<0.05),在>35岁患者中,25(OH)D水平及妊娠率均无显著性差异。在≤35岁oPOI患者中,25(OH)D干预组的血清25(OH)D浓度和优质胚胎率显著高于25(OH)D未干预组,差异具有统计学意义(42.13±12.91 vs 78.26±23.91,55.74±25.16 vs 80.39±29.05,P<0.05),但两组间的获卵数、受精率、临床妊娠率和着床率均没有显著差异;在>35岁的oPOI患者中,25(OH)D干预组与未干预组的血清25(OH)D浓度、获卵数、受精率、优质胚胎率、临床妊娠率和着床率均未见显著差异。结论≤35岁的女性不孕患者中,oPOI患者的维生素D水平低于其他因素不孕的患者,给予维生素D补充后可改善oPOI患者25(OH)D水平及优质胚胎率,但未改变oPOI患者的妊娠结局。展开更多
目的:探讨儿童原发性激素敏感型肾病综合征(SSNS)患儿血清25羟基维生素D_(3)[25-(OH)D_(3)]与T淋巴细胞亚群及实验室相关指标的表达水平特点及相关性。方法:选取2021年8月—2022年8月在山西省儿童医院肾内科初治的确诊为原发性肾病综合...目的:探讨儿童原发性激素敏感型肾病综合征(SSNS)患儿血清25羟基维生素D_(3)[25-(OH)D_(3)]与T淋巴细胞亚群及实验室相关指标的表达水平特点及相关性。方法:选取2021年8月—2022年8月在山西省儿童医院肾内科初治的确诊为原发性肾病综合征且经过标准剂量激素治疗4周后尿蛋白阴转的SSNS组患儿45例。同时选取同期年龄、性别相匹配的健康对照组儿童30例。比较两组儿童血清25-(OH)D_(3)、T淋巴细胞亚群、血浆白蛋白(Alb)、血脂测定[总胆固醇(TC)、三酰甘油(TG)]及24 h尿蛋白定量(24 h TPU)水平,分析25-(OH)D_(3)与T淋巴细胞亚群及实验室相关指标的相关性。结果:(1)SSNS组血清25-(OH)D_(3)、Treg细胞、CD_(3)^(+)CD_(8)^(+)(%)、Alb水平均低于健康对照组,差异有统计学意义(P<0.05);24 h TPU、TC、TG、CD_(3)^(+)CD_(4)^(+)(%)、CD_(4)^(+)/CD_(8)^(+)均高于健康对照组,差异有统计学意义(P<0.05)。(2)SSNS组中,血清25-(OH)D_(3)与Treg细胞、CD_(4)^(+)/CD_(8)^(+)、Alb水平呈正相关(β=0.335、0.458、0.343,P<0.05),与CD_(3)^(+)CD_(8)^(+)(%)、24 h TPU、TG、TC呈负相关(β=-0.437、-0.323、-0.325、-0.325,P<0.05)。结论:SSNS患儿存在25-(OH)D_(3)降低及T淋巴细胞亚群失衡,25-(OH)D_(3)与CD_(8)^(+)、CD_(4)^(+)/CD_(8)^(+)、Treg细胞、24 h TPU、Alb、血脂代谢密切相关。展开更多
Objective To study the effect of oral vitamin D (VD) supplementation on VD status and serum lipid in Chinese obese and healthy normal-weight men. Methods Twenty-one obese men with their body mass index (BMI)〉28 k...Objective To study the effect of oral vitamin D (VD) supplementation on VD status and serum lipid in Chinese obese and healthy normal-weight men. Methods Twenty-one obese men with their body mass index (BMI)〉28 kg/m2 served as an obese group and 22 healthy normal-weight men with their BMI〈24 kg/m2 served as a control group in this study. After they were given 50 000 IU of oral VD, once a week for 8 weeks, the serum 25-hydroxyvitamin D [25(OH)D] concentration was measured with an enzyme-immunoassay kit. Results After oral VD supplementation, the serum 25(OH)D concentration significantly increased from 46.1+9.1 nmol/L to 116.7_+20.3 nmol/L in the obese subjects (P〈O.01) and from 52.8_+17.8 nmol/L to 181.3_+30.2 nmol/L in the control ones (P=0.13). The serum high-density lipoprotein cholesterol (HDL-C) level was reduced within the normal reference range in the obese group. However, no significant change was observed in the level of other serum lipids (triglycerides, total cholesterol, and low-density lipoprotein cholesterol) in either of the two groups. Conclusion The effect of high-dose oral VD supplementation is weaker on VD status in the obese group than in the control group. High-dose oral VD supplementation has no side effect on serum lipid level in obese and control groups.展开更多
文摘目的:对25(OH)D3、甲状旁腺激素(PTH)与慢性心力衰竭心衰(CHF)严重程度的相关性进行系统研究。方法:选取住院CHF患者186例,其中HFpEF 96例,HFmrEF 30例,HFrEF 60例;研究同时选取同期健康人群42例作为对照组,收集一般资料、血清25(OH)D3、PTH、NT-proBNP水平、常规生化指标、心脏彩超结果等,另根据CHF组患者的不同亚型将186例CHF患者分为HFpEF组(96例患者)、HFmrEF组(30例患者)和HFrEF组(60例患者),对比HFpEF组、HFmrEF组和HFrEF组患者血清25(OH)D3和PTH表达水平差异,并进行统计分析。结果:CHF组和对照组一般资料和常规生化指标等资料对比差异无统计学意义(P > 0.05);而CHF组和对照组在25(OH)D3、PTH以及NT-proBNP等资料对比差异有统计学意义(P 3表达水平与CHF疾病的发生呈负相关(r = −0.442, P r = 0.521, P 3表达水平明显低于HFpEF组和HFmrEF组,而PTH表达水平明显高于HFpEF组和HFmrEF组(P P > 0.05)。结论:25‐羟维生素D3和PTH表达水平与心衰严重程度密切相关。25‐羟维生素D3和PTH联合检测对CHF疾病的诊断及病情严重程度评估具有重要的临床意义。
文摘目的研究血清中25(OH)D水平对隐匿型原发性卵巢功能不全(occult primary ovarian insufficiency,oPOI)患者妊娠结局的影响。方法回顾性分析2018年9月至2022年12月在广东省妇幼保健院生殖中心行辅助生殖治疗的218例患者的临床资料。将符合纳入标准的对照组和oPOI组患者按孕产妇的年龄节点分为≤35岁和>35岁,比较各组的25(OH)D浓度及妊娠结局的差异,随后对oPOI患者进行维生素D补充,追踪助孕结局。结果在≤35岁患者中,oPOI组的25(OH)D水平及妊娠率显著低于对照组(41.62±11.90 vs 63.04±16.26,42.37±4.62 vs 53.33±1.97,P<0.05),在>35岁患者中,25(OH)D水平及妊娠率均无显著性差异。在≤35岁oPOI患者中,25(OH)D干预组的血清25(OH)D浓度和优质胚胎率显著高于25(OH)D未干预组,差异具有统计学意义(42.13±12.91 vs 78.26±23.91,55.74±25.16 vs 80.39±29.05,P<0.05),但两组间的获卵数、受精率、临床妊娠率和着床率均没有显著差异;在>35岁的oPOI患者中,25(OH)D干预组与未干预组的血清25(OH)D浓度、获卵数、受精率、优质胚胎率、临床妊娠率和着床率均未见显著差异。结论≤35岁的女性不孕患者中,oPOI患者的维生素D水平低于其他因素不孕的患者,给予维生素D补充后可改善oPOI患者25(OH)D水平及优质胚胎率,但未改变oPOI患者的妊娠结局。
文摘目的:探讨儿童原发性激素敏感型肾病综合征(SSNS)患儿血清25羟基维生素D_(3)[25-(OH)D_(3)]与T淋巴细胞亚群及实验室相关指标的表达水平特点及相关性。方法:选取2021年8月—2022年8月在山西省儿童医院肾内科初治的确诊为原发性肾病综合征且经过标准剂量激素治疗4周后尿蛋白阴转的SSNS组患儿45例。同时选取同期年龄、性别相匹配的健康对照组儿童30例。比较两组儿童血清25-(OH)D_(3)、T淋巴细胞亚群、血浆白蛋白(Alb)、血脂测定[总胆固醇(TC)、三酰甘油(TG)]及24 h尿蛋白定量(24 h TPU)水平,分析25-(OH)D_(3)与T淋巴细胞亚群及实验室相关指标的相关性。结果:(1)SSNS组血清25-(OH)D_(3)、Treg细胞、CD_(3)^(+)CD_(8)^(+)(%)、Alb水平均低于健康对照组,差异有统计学意义(P<0.05);24 h TPU、TC、TG、CD_(3)^(+)CD_(4)^(+)(%)、CD_(4)^(+)/CD_(8)^(+)均高于健康对照组,差异有统计学意义(P<0.05)。(2)SSNS组中,血清25-(OH)D_(3)与Treg细胞、CD_(4)^(+)/CD_(8)^(+)、Alb水平呈正相关(β=0.335、0.458、0.343,P<0.05),与CD_(3)^(+)CD_(8)^(+)(%)、24 h TPU、TG、TC呈负相关(β=-0.437、-0.323、-0.325、-0.325,P<0.05)。结论:SSNS患儿存在25-(OH)D_(3)降低及T淋巴细胞亚群失衡,25-(OH)D_(3)与CD_(8)^(+)、CD_(4)^(+)/CD_(8)^(+)、Treg细胞、24 h TPU、Alb、血脂代谢密切相关。
基金supported by grants from Danone Institute,China Diet Nutrition Research & Communication (DIC2010-03)National Natural Science Foundation of China (81172669)+1 种基金Medical Scientific Research Foundation of Guangdong Province (A2012581)National Key Technology Research and Development Program of China (2012BAI02B02)
文摘Objective To study the effect of oral vitamin D (VD) supplementation on VD status and serum lipid in Chinese obese and healthy normal-weight men. Methods Twenty-one obese men with their body mass index (BMI)〉28 kg/m2 served as an obese group and 22 healthy normal-weight men with their BMI〈24 kg/m2 served as a control group in this study. After they were given 50 000 IU of oral VD, once a week for 8 weeks, the serum 25-hydroxyvitamin D [25(OH)D] concentration was measured with an enzyme-immunoassay kit. Results After oral VD supplementation, the serum 25(OH)D concentration significantly increased from 46.1+9.1 nmol/L to 116.7_+20.3 nmol/L in the obese subjects (P〈O.01) and from 52.8_+17.8 nmol/L to 181.3_+30.2 nmol/L in the control ones (P=0.13). The serum high-density lipoprotein cholesterol (HDL-C) level was reduced within the normal reference range in the obese group. However, no significant change was observed in the level of other serum lipids (triglycerides, total cholesterol, and low-density lipoprotein cholesterol) in either of the two groups. Conclusion The effect of high-dose oral VD supplementation is weaker on VD status in the obese group than in the control group. High-dose oral VD supplementation has no side effect on serum lipid level in obese and control groups.