Skoczek-Rubińska Aleksandra, Cisek-Woźniak Angelika, Molska Marta, Heyser Martyna, Trocholepsza Martyna, Pietrzak Sebastian, Mruczyk Kinga
Department of Dietetics, Faculty of Physical Culture in Gorzów Wielkopolski, Poznan University of Physical Education, 66-400 Gorzów Wielkopolski, Poland.
Sebastian Pietrzak Company, 66-400 Gorzów Wielkopolski, Poland.
Nutrients. 2025 Aug 16;17(16):2655. doi: 10.3390/nu17162655.
BACKGROUND/OBJECTIVES: Vitamin D deficiency is prevalent in higher-latitude regions and among older adults, and has been linked to depressive symptoms and cognitive decline, although the neurobiological link remains unclear. Brain-derived neurotrophic factor (BDNF) may be a key modulator and mediator of vitamin D-related neuroprotection.
Selected databases (2009-2025) were searched for specific studies reporting vitamin D exposure, BDNF, and mood or cognitive outcomes. Risk of bias was appraised with RoB 2, Newcastle-Ottawa Scale or SYRCLE.
Thirteen studies were included. High-dose vitamin D improves mood primarily when levels are low. Supplementation of at least 2000 IU/day for 12 weeks reduced BDI scores by 1.7-7.6 points and increased BDNF levels by ~7%. Each 1 ng/mL increase in 25(OH)D levels decreased the likelihood of depressive symptoms, especially when BDNF levels were high. In animal studies vitamin D increases hippocampal BDNF and reverses stress-induced depressive behavioral deficits. Adequate vitamin D intake is associated with improved cognitive performance and a dose-dependent increase in BDNF. Each 10 ng/mL increase in 25(OH)D was associated with a 0.6-point increase in MMSE scores and a 15% increase in serum BDNF. Low vitamin D status in children may predict cognitive decline. Animal studies have shown that supplementation with 500-10,000 IU/kg for at least 3 weeks increased hippocampal BDNF and improved biochemical markers of aging.
Vitamin D supplementation may support mood and cognition via BDNF modulation, especially in people with insufficient vitamin D levels (<30 ng/mL), but long-term, adequately powered studies with objective tools are required.
背景/目的:维生素D缺乏在高纬度地区和老年人中普遍存在,并且与抑郁症状和认知衰退有关,尽管其神经生物学联系尚不清楚。脑源性神经营养因子(BDNF)可能是维生素D相关神经保护的关键调节因子和介质。
检索选定的数据库(2009 - 2025年),查找报告维生素D暴露、BDNF以及情绪或认知结果的特定研究。使用RoB 2、纽卡斯尔-渥太华量表或SYRCLE评估偏倚风险。
纳入13项研究。高剂量维生素D主要在水平较低时改善情绪。每天补充至少2000 IU,持续12周,可使BDI评分降低1.7 - 7.6分,并使BDNF水平提高约7%。25(OH)D水平每升高1 ng/mL,抑郁症状的可能性降低,尤其是当BDNF水平较高时。在动物研究中,维生素D可增加海马体中的BDNF,并逆转应激诱导的抑郁行为缺陷。充足的维生素D摄入量与改善认知表现以及BDNF的剂量依赖性增加有关。25(OH)D每升高10 ng/mL,与MMSE评分增加0.6分以及血清BDNF增加15%相关。儿童维生素D水平低可能预示认知衰退。动物研究表明,补充500 - 10,000 IU/kg至少3周可增加海马体中的BDNF,并改善衰老的生化指标。
补充维生素D可能通过调节BDNF来支持情绪和认知,特别是在维生素D水平不足(<30 ng/mL)的人群中,但需要长期、有足够样本量且使用客观工具的研究。