{"title":"维生素D缺乏及其在多发性硬化中的可能作用","authors":"M. Holick, S. Cook, G. Suárez, M. Rametta","doi":"10.17925/ENR.2015.10.02.131","DOIUrl":null,"url":null,"abstract":"TOUCH MEDICAL MEDIA • Despite a lack of consensus, vitamin D deficiency and insufficiency have been defined as a serum level of 25-hydroxyvitamin D (25[OH]D) <50 nmol/L or 52.5–72.5 nmol/L respectively. • Vitamin D deficiency is widespread. • Vitamin D is probably involved in the prevention of numerous disease states. • Most primary care clinicians are unaware of the recommended dose for vitamin D supplementation or the optimum serum level in multiple sclerosis (MS) patients. • In the general population management of vitamin D deficiency in children and adults can be effectively achieved by administering 50,000 IU vitamin D2 or vitamin D3 once a week for 6 or 8 weeks respectively: – In the general population 600–1,000 IU/d is effective to prevent recurrence in children and 50,000 IU vitamin D3 or vitamin D2 every 2 weeks (equivalent to approximately 3,600 IU daily) in adults. This strategy maintains blood levels of 25(OH)D at approximately 100–150 nmol/L for up to 6 years with no evidence of toxicity. – In pregnant women supplementation with 2,000 and 4,000 IU/d during pregnancy improve maternal/ neonatal vitamin D status. • Considerable evidence exists for the protective effects of vitamin D in MS, with higher sun exposure and vitamin D intake associated with a lower risk of MS. • Improvement in 25(OH)D status appears to additively enhance the beneficial effects of interferon-beta. To date, this effect has not as yet been observed with glatiramer acetate. • Results from the Betaferon/Betaseron in Newly Emerging multiple sclerosis For Initial Treatment (BENEFIT) study showed that patients with vitamin D levels (25[OH]D) <50 nmol/L had more prominent clinical and MRI disease activity.","PeriodicalId":12047,"journal":{"name":"European neurological review","volume":"10 1","pages":"131"},"PeriodicalIF":0.0000,"publicationDate":"2015-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"6","resultStr":"{\"title\":\"Vitamin D Deficiency and Possible Role in Multiple Sclerosis\",\"authors\":\"M. Holick, S. Cook, G. Suárez, M. Rametta\",\"doi\":\"10.17925/ENR.2015.10.02.131\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"TOUCH MEDICAL MEDIA • Despite a lack of consensus, vitamin D deficiency and insufficiency have been defined as a serum level of 25-hydroxyvitamin D (25[OH]D) <50 nmol/L or 52.5–72.5 nmol/L respectively. • Vitamin D deficiency is widespread. • Vitamin D is probably involved in the prevention of numerous disease states. • Most primary care clinicians are unaware of the recommended dose for vitamin D supplementation or the optimum serum level in multiple sclerosis (MS) patients. • In the general population management of vitamin D deficiency in children and adults can be effectively achieved by administering 50,000 IU vitamin D2 or vitamin D3 once a week for 6 or 8 weeks respectively: – In the general population 600–1,000 IU/d is effective to prevent recurrence in children and 50,000 IU vitamin D3 or vitamin D2 every 2 weeks (equivalent to approximately 3,600 IU daily) in adults. This strategy maintains blood levels of 25(OH)D at approximately 100–150 nmol/L for up to 6 years with no evidence of toxicity. – In pregnant women supplementation with 2,000 and 4,000 IU/d during pregnancy improve maternal/ neonatal vitamin D status. • Considerable evidence exists for the protective effects of vitamin D in MS, with higher sun exposure and vitamin D intake associated with a lower risk of MS. • Improvement in 25(OH)D status appears to additively enhance the beneficial effects of interferon-beta. To date, this effect has not as yet been observed with glatiramer acetate. • Results from the Betaferon/Betaseron in Newly Emerging multiple sclerosis For Initial Treatment (BENEFIT) study showed that patients with vitamin D levels (25[OH]D) <50 nmol/L had more prominent clinical and MRI disease activity.\",\"PeriodicalId\":12047,\"journal\":{\"name\":\"European neurological review\",\"volume\":\"10 1\",\"pages\":\"131\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2015-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"6\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"European neurological review\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.17925/ENR.2015.10.02.131\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"European neurological review","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.17925/ENR.2015.10.02.131","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
Vitamin D Deficiency and Possible Role in Multiple Sclerosis
TOUCH MEDICAL MEDIA • Despite a lack of consensus, vitamin D deficiency and insufficiency have been defined as a serum level of 25-hydroxyvitamin D (25[OH]D) <50 nmol/L or 52.5–72.5 nmol/L respectively. • Vitamin D deficiency is widespread. • Vitamin D is probably involved in the prevention of numerous disease states. • Most primary care clinicians are unaware of the recommended dose for vitamin D supplementation or the optimum serum level in multiple sclerosis (MS) patients. • In the general population management of vitamin D deficiency in children and adults can be effectively achieved by administering 50,000 IU vitamin D2 or vitamin D3 once a week for 6 or 8 weeks respectively: – In the general population 600–1,000 IU/d is effective to prevent recurrence in children and 50,000 IU vitamin D3 or vitamin D2 every 2 weeks (equivalent to approximately 3,600 IU daily) in adults. This strategy maintains blood levels of 25(OH)D at approximately 100–150 nmol/L for up to 6 years with no evidence of toxicity. – In pregnant women supplementation with 2,000 and 4,000 IU/d during pregnancy improve maternal/ neonatal vitamin D status. • Considerable evidence exists for the protective effects of vitamin D in MS, with higher sun exposure and vitamin D intake associated with a lower risk of MS. • Improvement in 25(OH)D status appears to additively enhance the beneficial effects of interferon-beta. To date, this effect has not as yet been observed with glatiramer acetate. • Results from the Betaferon/Betaseron in Newly Emerging multiple sclerosis For Initial Treatment (BENEFIT) study showed that patients with vitamin D levels (25[OH]D) <50 nmol/L had more prominent clinical and MRI disease activity.