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钴胺素缺乏、高同型半胱氨酸血症与痴呆。

Cobalamin deficiency, hyperhomocysteinemia, and dementia.

机构信息

Kansas University School of Medicine - Wichita, Wichita, KS, USA.

出版信息

Neuropsychiatr Dis Treat. 2010 May 6;6:159-95. doi: 10.2147/ndt.s6564.

Abstract

INTRODUCTION

Although consensus guidelines recommend checking serum B12 in patients with dementia, clinicians are often faced with various questions: (1) Which patients should be tested? (2) What test should be ordered? (3) How are inferences made from such testing? (4) In addition to serum B12, should other tests be ordered? (5) Is B12 deficiency compatible with dementia of the Alzheimer's type? (6) What is to be expected from treatment? (7) How is B12 deficiency treated?

METHODS

On January 31st, 2009, a Medline search was performed revealing 1,627 citations related to cobalamin deficiency, hyperhomocysteinemia, and dementia. After limiting the search terms, all abstracts and/or articles and other references were categorized into six major groups (general, biochemistry, manifestations, associations and risks, evaluation, and treatment) and then reviewed in answering the above questions.

RESULTS

The six major groups above are described in detail. Seventy-five key studies, series, and clinical trials were identified. Evidence-based suggestions for patient management were developed.

DISCUSSION

Evidence is convincing that hyperhomocysteinemia, with or without hypovitaminosis B12, is a risk factor for dementia. In the absence of hyperhomocysteinemia, evidence is less convincing that hypovitaminosis B12 is a risk factor for dementia. B12 deficiency manifestations are variable and include abnormal psychiatric, neurological, gastrointestinal, and hematological findings. Radiological images of individuals with hyperhomocysteinemia frequently demonstrate leukoaraiosis. Assessing serum B12 and treatment of B12 deficiency is crucial for those cases in which pernicious anemia is suspected and may be useful for mild cognitive impairment and mild to moderate dementia. The serum B12 level is the standard initial test: 200 picograms per milliliter or less is low, and 201 to 350 picograms per milliliter is borderline low. Other tests may be indicated, including plasma homocysteine, serum methylmalonic acid, antiparietal cell and anti-intrinsic factor antibodies, and serum gastrin level. In B12 deficiency dementia with versus without pernicious anemia, there appear to be different manifestations, need for further workup, and responses to treatment. Dementia of the Alzheimer's type is a compatible diagnosis when B12 deficiency is found, unless it is caused by pernicious anemia. Patients with pernicious anemia generally respond favorably to supplemental B12 treatment, especially if pernicious anemia is diagnosed early in the course of the disease. Some patients without pernicious anemia, but with B12 deficiency and either mild cognitive impairment or mild to moderate dementia, might show some degree of cognitive improvement with supplemental B12 treatment. Evidence that supplemental B12 treatment is beneficial for patients without pernicious anemia, but with B12 deficiency and moderately-severe to severe dementia is scarce. Oral cyanocobalamin is generally favored over intramuscular cyanocobalamin.

摘要

简介

尽管共识指南建议在痴呆患者中检查血清 B12,但临床医生经常面临各种问题:(1)应检查哪些患者?(2)应订购哪些检查?(3)如何从这些检查中得出推论?(4)除了血清 B12,还应订购其他检查吗?(5)B12 缺乏症是否与阿尔茨海默病型痴呆兼容?(6)可以期待什么样的治疗效果?(7)如何治疗 B12 缺乏症?

方法

2009 年 1 月 31 日,进行了 Medline 搜索,揭示了与钴胺素缺乏,高同型半胱氨酸血症和痴呆有关的 1627 条引文。在限制搜索词后,将所有摘要和/或文章和其他参考文献分为六个主要组(一般,生化,表现,关联和风险,评估和治疗),然后对其进行了回顾,以回答上述问题。

结果

详细描述了上述六个主要组。确定了 75 项关键研究,系列和临床试验。为患者管理制定了循证建议。

讨论

有令人信服的证据表明,高同型半胱氨酸血症,无论是否伴有维生素 B12 缺乏,都是痴呆症的危险因素。在没有高同型半胱氨酸血症的情况下,证据不太令人信服,表明维生素 B12 缺乏症是痴呆症的危险因素。B12 缺乏症的表现多种多样,包括异常的精神,神经,胃肠道和血液学发现。高同型半胱氨酸血症患者的影像学图像经常显示出脑白质疏松症。评估血清 B12 和治疗 B12 缺乏症对于怀疑恶性贫血的病例至关重要,并且可能对轻度认知障碍和轻度至中度痴呆症有用。血清 B12 水平是标准的初始检查:每毫升 200 皮克或更低为低,201 至 350 皮克/毫升为边缘低。其他检查可能包括血浆同型半胱氨酸,血清甲基丙二酸,壁细胞和内因子抗体以及血清胃泌素水平。在伴有或不伴有恶性贫血的 B12 缺乏性痴呆症中,似乎存在不同的表现,需要进一步检查以及对治疗的反应。当发现 B12 缺乏症时,阿尔茨海默病型痴呆症是一种相容的诊断,除非它是由恶性贫血引起的。恶性贫血患者通常对补充 B12 治疗有良好的反应,尤其是在疾病早期诊断出恶性贫血时。一些没有恶性贫血但 B12 缺乏且有轻度认知障碍或轻度至中度痴呆症的患者,可能会因补充 B12 治疗而在认知上有一定程度的改善。缺乏恶性贫血但有 B12 缺乏和中度至重度痴呆症的患者补充 B12 治疗有益的证据很少。口服氰钴胺通常优于肌肉内氰钴胺。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f668/2874340/a07349ae6355/ndt-6-159f1.jpg

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