年龄和性别对非退行性帕金森病患者纹状体多巴胺转运体密度和脑灌注的影响:18F-FP-CIT PET 双相研究。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Ji-Young Kim, Seo Young Kang, Byung Seok Moon, Bom Sahn Kim, Jee Hyang Jeong, Hai-Jeon Yoon
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引用次数: 0

摘要

背景:双相氟-18标记的N-3-氟丙基-2β-碳甲氧基-3β-(4-碘苯基)正丙烷(18F-FP-CIT)正电子发射断层扫描(PET)可用于支持帕金森病(PD)等疾病。多巴胺转运体(DAT)结合和脑灌注与年龄和性别有关。我们研究了年龄和性别对非退行性帕金森病的影响,在纹状体中使用了自动量化技术:延迟期 PET(dCIT)中 DAT 结合的特异性结合率(SBR)和早期 PET(eCIT)中脑灌注的标准化摄取值比(SUVR)。我们还研究了 SBR 和 SUVR 之间的相关性:这项回顾性研究分析了接受双相 18F-FP-CIT PET 扫描的受试者。eCIT 图像在注射后立即采集,dCIT 图像在 120 分钟后采集。利用 Brightonix 软件,从视觉正常的扫描图像中自动量化了 dCIT 的 SBR 和 eCIT 的 SUVR。通过将 SBR 和 SUVR 与年龄进行回归,评估了衰老和性别的影响。评估了 SUVR 与 SBR 之间的相关性:我们研究了 79 名受试者(34 名男性和 45 名女性)。在背侧纹状体、腹侧纹状体、尾状核和普坦中观察到与年龄相关的 SBRs 减少。研究发现,男性背侧纹状体、腹侧纹状体、尾状核和丘脑的 SUVR 与年龄呈负相关,女性背侧纹状体和尾状核的 SUVR 与年龄呈正相关。男性背侧纹状体、腹侧纹状体、尾状核和丘脑,女性背侧纹状体、尾状核和丘脑的SBR与SUVR之间呈正相关:利用单次注射的双相18F-FP-CIT PET的量化值,我们证明了年龄对男女性纹状体中的SBRs(DAT结合)和男女性背侧纹状体和尾状核以及男性腹侧纹状体和正中丘脑中的SUVRs(脑灌注)的负面影响。此外,我们还发现 SBR 与背侧纹状体、尾状核和丘脑的 SUVR 值之间存在正相关,其中背侧纹状体、尾状核和丘脑的 SUVR 值与腹侧纹状体的 SUVR 值之间存在正相关,而腹侧纹状体和丘脑的 SUVR 值与男性的 SUVR 值之间存在正相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Age and gender effects on striatal dopamine transporter density and cerebral perfusion in individuals with non-degenerative parkinsonism: a dual-phase 18F-FP-CIT PET study.

Background: Dual-phase fluorine-18 labeled N-3-fluoropropyl-2β-carbomethoxy-3β-(4-iodophenyl) nortropane (18F-FP-CIT) positron emission tomography (PET) scans could be used to support disorders like Parkinson's disease (PD). Dopamine transporter (DAT) binding and cerebral perfusion are associated with ageing and gender. We investigated the effects of age and gender on non-degenerative parkinsonism, using automated quantification in striatum: specific binding ratios (SBRs) for DAT binding in delayed phase PET (dCIT) and standardized-uptake-value ratios (SUVRs) for cerebral perfusion in early phase PET (eCIT). We also examined the correlations between SBR and SUVR.

Methods: This retrospective study analyzed subjects with dual-phase 18F-FP-CIT PET scans. The eCIT images were acquired immediately post-injection, and dCIT images were taken 120 min later. With Brightonix software, automated quantification of SBRs for dCIT and SUVRs for eCIT were acquired from visually normal scans. The effects of aging and gender were assessed by regressing SBRs and SUVRs on age for both genders. The correlations between SUVRs and SBRs were evaluated.

Results: We studied 79 subjects (34 males and 45 females). An age-related reduction in SBRs was observed in the dorsal striatum, ventral striatum, caudate nucleus, and putamen for both genders. SUVRs were found to negatively correlate with age in the dorsal striatum, ventral striatum, caudate nucleus, and putamen for males and in the dorsal striatum and caudate nucleus for females. Positive correlations between SBRs and SUVRs in the dorsal striatum, ventral striatum, caudate nucleus, and putamen for male and in the dorsal striatum, caudate nucleus, and putamen for females.

Conclusions: Using quantified values from dual-phase 18F-FP-CIT PET with a single injection, we demonstrate a negative impact of age on SBRs (DAT binding) in the striatum for both genders and SUVRs (cerebral perfusion) in the dorsal striatum and caudate nucleus for both genders and in the ventral striatum and putamen for males. Additionally, we found positive associations between SBR and SUVR values in the dorsal striatum, caudate nucleus, and putamen for both genders and in the ventral striatum for males.

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