Discrepancy between regional cerebral blood flow and glucose metabolism of the brain in systemic lupus erythematosus patients with normal brain magnetic resonance imaging findings

IF 10.9 1区 医学 Q1 RHEUMATOLOGY Arthritis & Rheumatology Pub Date : 2001-05-22 DOI:10.1002/1529-0131(199901)42:1<61::AID-ANR8>3.0.CO;2-9
Chia-Hung Kao, Yung-Jen Ho, Jung-Liang Lan, Sheng-Ping Changlai, Ko-Kaung Liao, Poon-Ung Chieng
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引用次数: 86

Abstract

Objective

In this study, 2 updated brain-imaging modalities, technetium-99m hexamethylpropylene amine oxime–single-photon–emission computed tomography (HMPAO-SPECT) and fluorine-18 2-fluoro-2-deoxy-D-glucose–positron emission tomography (FDG-PET), were used to simultaneously detect regional cerebral blood flow (rCBF) and glucose metabolism of the brain in patients with systemic lupus erythematosus (SLE).

Methods

Twenty-five female SLE patients, ages 25–40 years, were enrolled in this study and assigned to 1 of 2 groups. Group 1 consisted of 13 patients with neuropsychiatric manifestations (7 had major and 6 had minor manifestations). Group 2 consisted of 12 patients without neuropsychiatric manifestations. Serum levels of anticardiolipin antibodies (aCL) and anti–ribosomal P antibodies (anti-P) were measured. All patients had normal brain magnetic resonance imaging (MRI) findings. Ten healthy female volunteers also underwent brain MRI, HMPAO-SPECT, and FDG-PET for comparison.

Results

99mTc-HMPAO-SPECT revealed hypoperfusion lesions in 11 (44%) of 25 SLE patients, including 9 (69%) of the 13 patients in group 1, 7 (100%) of the 7 patients with major manifestations, 2 (33%) of the 6 patients with minor manifestations, and 2 (17%) of the 12 patients in group 2. Parietal lobes were the areas most commonly involved. FDG-PET revealed hypometabolism in 7 (54%) of the group 1 patients, 6 (86%) of the 7 patients with major manifestations, and 1 (17%) of the 6 patients with minor manifestations. Temporal lobes were the most commonly involved areas. However, no significant hypometabolism brain lesions were found in group 2 patients. All of the 4 patients with headaches and dizziness or headaches alone had normal findings on HMPAO-SPECT and FDG-PET. Nine (36%) of the 25 patients were positive for aCL. However, the presence of aCL was not related to neuropsychiatric manifestations or to HMPAO-SPECT or FDG-PET findings. Five (20%) of the 25 patients had anti-P antibodies and psychosis/depression.

Conclusion

In patients with normal brain MRI findings, decreases in glucose metabolism coupled with decreases in rCBF are associated with serious neuropsychiatric SLE (NPSLE) presentations, while normal glucose metabolism with decreases in rCBF may be found in SLE patients with or without NPSLE.

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脑磁共振成像正常的系统性红斑狼疮患者脑区域血流量和脑糖代谢的差异
目的采用两种最新的脑成像方式,即锝-99m六亚甲基丙烯胺肟-单光子发射计算机断层扫描(hpao - spect)和氟-18 2-氟-2-脱氧-d -葡萄糖-正电子发射断层扫描(FDG-PET),同时检测系统性红斑狼疮(SLE)患者的脑区域血流量(rCBF)和脑葡萄糖代谢。方法选取25例女性SLE患者,年龄25 ~ 40岁,分为2组。第一组有神经精神表现的患者13例,其中重度7例,轻度6例。第二组12例无神经精神症状。测定血清抗心磷脂抗体(aCL)和抗核糖体P抗体(anti-P)水平。所有患者的脑磁共振成像(MRI)结果正常。10名健康女性志愿者也接受了脑MRI、hpao - spect和FDG-PET进行比较。结果25例SLE患者中,99mtc - hpao - spect显示低灌注病变11例(44%),其中1组13例患者中9例(69%),7例主要表现患者中7例(100%),6例轻微表现患者中2例(33%),2组12例患者中2例(17%)。顶叶是最常受累的区域。FDG-PET显示1组7例(54%)、7例重度表现患者6例(86%)、6例轻度表现患者1例(17%)存在低代谢。颞叶是最常见的受累区域。然而,2组患者未发现明显的低代谢脑损伤。4例头痛合并头晕或单纯头痛患者hpao - spect和FDG-PET检查均正常。25例患者中有9例(36%)aCL阳性。然而,aCL的存在与神经精神表现或hpao - spect或FDG-PET结果无关。25例患者中有5例(20%)存在抗p抗体和精神病/抑郁症。在脑MRI表现正常的患者中,糖代谢降低并rCBF减少与严重的神经精神性SLE (NPSLE)表现相关,而在伴有或不伴有NPSLE的SLE患者中,可能发现糖代谢正常但rCBF减少。
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来源期刊
Arthritis & Rheumatology
Arthritis & Rheumatology RHEUMATOLOGY-
CiteScore
20.90
自引率
3.00%
发文量
371
期刊介绍: Arthritis & Rheumatology is the official journal of the American College of Rheumatology and focuses on the natural history, pathophysiology, treatment, and outcome of rheumatic diseases. It is a peer-reviewed publication that aims to provide the highest quality basic and clinical research in this field. The journal covers a wide range of investigative areas and also includes review articles, editorials, and educational material for researchers and clinicians. Being recognized as a leading research journal in rheumatology, Arthritis & Rheumatology serves the global community of rheumatology investigators and clinicians.
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