Shahid Beheshti University of Medical Sciences, International Branch, Tehran, Iran.
J Am Coll Nutr. 2013;32(1):26-30. doi: 10.1080/07315724.2013.767659.
Cardiovascular disease (CVD) is the major morbidity and cause of death in diabetic subjects. Observational studies have shown the association of low vitamin D status with poor glycemic control, atherogenic lipid profile, and CVD. However, the possible link between circulating 25-hydroxycholecalciferol and apoproteins (Apo A1 and B) and the atherogenic lipoprotein (a) [Lp(a)] has not been documented to date.
Ninety subjects with type 2 diabetes (T2D) aged 30-60 years from both sexes were randomly allocated to one of the 3 groups to receive 2 bottles a day of either (1) plain doogh (PD; containing 150 mg calcium and no detectable vitamin D/250 mL); (2) vitamin D-fortified doogh (DD; containing 150 mg calcium and 500 IU vitamin D/250 mL); or (3) calcium- and vitamin D-fortified doogh (CDD; containing 250 mg calcium and 500 IU vitamin D/250 mL) for 12 weeks. Anthropometric, dietary, and laboratory assessments, including Apo A1, Apo B, and Lp(a), were done.
Improvement of vitamin D status in DD and CDD groups, compared to PD, resulted in a significant increase in Apo A1 (mean changes 0.22 ± 0.38, 0.20 ± 0.27 and 0.01 ± 0.35 g/L, respectively, p = 0.047) and a significant decrease in serum Lp(a) (mean changes -0.08 ± 0.30, -0.08 ± 0.31, and 0.14 ± 0.25 μmol/L, respectively, p = 0.011). There was no significant difference between DD and CDD groups. Serum Apo B did not change significantly in any of the groups.
Significant amelioration of serum Apo A1 and Lp(a) following improvement of vitamin D status in T2D subjects may have preventive implications against long-term diabetic complications, notably CVD. This trial was registered at ClinicalTrials.gov as NTC01229891.
心血管疾病(CVD)是糖尿病患者的主要发病率和死亡原因。观察性研究表明,维生素 D 状态低下与血糖控制不佳、致动脉粥样硬化脂质谱和 CVD 有关。然而,目前尚未记录到循环 25-羟胆钙化醇与载脂蛋白(Apo A1 和 B)和致动脉粥样脂蛋白(a)[Lp(a)]之间的可能联系。
将 90 名年龄在 30-60 岁的 2 型糖尿病(T2D)患者随机分配到以下 3 组中的一组,每天服用 2 瓶:(1)普通乳清(PD;含 150mg 钙,检测不到维生素 D/250mL);(2)维生素 D 强化乳清(DD;含 150mg 钙和 500IU 维生素 D/250mL);或(3)钙和维生素 D 强化乳清(CDD;含 250mg 钙和 500IU 维生素 D/250mL),共 12 周。进行人体测量、饮食和实验室评估,包括载脂蛋白 A1、载脂蛋白 B 和 Lp(a)。
与 PD 相比,DD 和 CDD 组维生素 D 状况的改善导致载脂蛋白 A1 显著增加(平均变化分别为 0.22±0.38、0.20±0.27 和 0.01±0.35g/L,p=0.047),血清 Lp(a)显著降低(平均变化分别为-0.08±0.30、-0.08±0.31 和 0.14±0.25μmol/L,p=0.011)。DD 和 CDD 组之间没有显著差异。各组血清载脂蛋白 B 均无明显变化。
T2D 患者维生素 D 状态改善后,血清 Apo A1 和 Lp(a)显著改善,可能对长期糖尿病并发症,特别是 CVD 具有预防意义。该试验在 ClinicalTrials.gov 上注册为 NTC01229891。