洪珊珊,趙中,韓伯軍,王慶廣,姜歧濤,鄭勇強(qiáng),劉定華
(1南京醫(yī)科大學(xué)附屬蘇州醫(yī)院,江蘇蘇州215001;2東南大學(xué)醫(yī)學(xué)院附屬江陰醫(yī)院)
酒依賴患者胼胝體纖維的磁共振彌散張量成像檢查結(jié)果分析
洪珊珊1,2,趙中1,韓伯軍2,王慶廣2,姜歧濤2,鄭勇強(qiáng)2,劉定華2
(1南京醫(yī)科大學(xué)附屬蘇州醫(yī)院,江蘇蘇州215001;2東南大學(xué)醫(yī)學(xué)院附屬江陰醫(yī)院)
目的 通過(guò)磁共振彌散張量成像的纖維跟蹤技術(shù),觀察分析酒依賴患者胼胝體纖維數(shù)量及結(jié)構(gòu)的變化。方法 酒依賴患者(病例組)48例,年齡、性別、受教育年限與之相匹配的正常志愿者(對(duì)照組)50例。對(duì)兩組患者進(jìn)行頭部T1加權(quán)三維磁共振成像及彌散張量成像檢查,計(jì)算并比較兩組胼胝體纖維數(shù)目及其各向異性分?jǐn)?shù)(FA)、表面擴(kuò)散系數(shù)(ADC)。結(jié)果 病例組總胼胝體纖維數(shù)為(2 587±654)條,對(duì)照組為(2 875±758)條,兩組相比,P<0.05;病例組胼胝體前1/3部纖維數(shù)目為(782±254)條,對(duì)照組為(987±244)條,兩組相比,P<0.01。病例組總胼胝體FA值為0.61±0.02,對(duì)照組為0.62±0.02,兩組相比,P<0.05;病例組胼胝體前1/3部FA值為0.59±0.03,對(duì)照組為0.61±0.03,兩組相比,P<0.01。病例組總胼胝體ADC值為(0.94±0.07)×10-3mm2/s,對(duì)照組為(0.91±0.07)×10-3mm2/s,兩組相比,P<0.05;病例組胼胝體前1/3部ADC值為(0.94±0.06)×10-3mm2/s,對(duì)照組為(0.87±0.08)×10-3mm2/s,兩組相比,P<0.01。結(jié)論 酒依賴患者胼胝體纖維數(shù)目及結(jié)構(gòu)異常,這種異常在胼胝體前1/3部纖維更明顯。
酒依賴;胼胝體;胼胝體纖維;磁共振成像;彌散張量成像;纖維跟蹤技術(shù)
Magnetic resonance diffusion tensor imaging of the fiber of corpus callosum in alcohol-dependent patients
酒依賴是不可忽視的社會(huì)問(wèn)題和醫(yī)學(xué)問(wèn)題。酒依賴可導(dǎo)致多種軀體疾病、精神障礙及認(rèn)知功能損害[1,2]。近年來(lái)隨著神經(jīng)影像學(xué)技術(shù)的不斷發(fā)展,為我們揭示了酒依賴的神經(jīng)生物學(xué)基礎(chǔ)。國(guó)外已有研究[3~5]發(fā)現(xiàn)酒依賴患者存在胼胝體結(jié)構(gòu)異常。然而迄今為止國(guó)內(nèi)尚無(wú)基于磁共振彌散張量成像(DTI)的纖維跟蹤技術(shù)研究酒依賴患者胼胝體纖維結(jié)構(gòu)的報(bào)道,本研究通過(guò)該技術(shù)對(duì)酒依賴患者胼胝體纖維的數(shù)量及結(jié)構(gòu)進(jìn)行了觀察。現(xiàn)將結(jié)果分析如下。
1.1 臨床資料 選取2009年8月~2014年8月東南大學(xué)醫(yī)學(xué)院附屬江陰醫(yī)院確診的酒依賴患者48例(病例組),男40例、女8例,年齡40~60歲,智商(92.59±8.43)分,受教育年限(12.4±3.5) a,日飲酒量(363.32±75.50)mL(受檢前近期日飲酒量200~700 mL),日飲酒量折合純酒精(185±67)g,持續(xù)飲酒時(shí)間(18.92±7.53)a。符合Sacanella關(guān)于慢性過(guò)量飲酒的標(biāo)準(zhǔn)[6]:每日飲酒中酒精量>100 g,連續(xù)飲酒超過(guò)24個(gè)月。符合國(guó)際疾病分類(ICD-10)酒依賴診斷標(biāo)準(zhǔn)及《中國(guó)精神障礙分類與診斷標(biāo)準(zhǔn)》(第3版)中酒精依賴綜合征的診斷標(biāo)準(zhǔn)。治療時(shí)間>1周,無(wú)明顯戒斷癥狀,排除重大軀體疾病、弱智、外傷、其他可能影響認(rèn)知的精神系統(tǒng)疾病等。同時(shí)在社區(qū)隨機(jī)招募正常志愿者50例(對(duì)照組),男38例、女12例,年齡41~58歲,智商評(píng)分(95.48±9.78)分,受教育年限(12.58±3.82) a年,無(wú)大量飲酒史,無(wú)意識(shí)障礙和精神障礙,通過(guò)詳細(xì)的體格檢查和精神檢查排除軀體疾病、神經(jīng)精神疾病。兩組受試者均為右利手,無(wú)特殊藥物服用史。兩組年齡、性別、智商、受教育年限有可比性(P均>0.05)。本研究均取得受檢者本人簽署的知情同意書(shū)并經(jīng)醫(yī)院醫(yī)學(xué)倫理委員會(huì)批準(zhǔn)。
1.2 磁共振DTI檢查及圖像處理與分析 受試者接受荷蘭飛利浦(中國(guó))PHILIPS ACHIEVA 3.0T超導(dǎo)型磁共振儀檢查。經(jīng)常規(guī)磁共振檢查定位并排除腦部肉眼可見(jiàn)病變后再行頭部軸位DTI檢查。DTI數(shù)據(jù)采集采用單次激發(fā)自旋回波EPI脈沖序列,具體參數(shù):TR 8 000 ms,TE 79.3 ms,矩陣128×128, FOV 24 cm×24 cm,層厚2 mm,層距0 mm,擴(kuò)散加權(quán)系數(shù)b=1 000 s/mm2,擴(kuò)散敏感梯度方向25個(gè),掃描時(shí)間5 min,掃描前進(jìn)行勻場(chǎng)以減少靜磁場(chǎng)強(qiáng)度不勻引起的圖像變形。
將DTI原始數(shù)據(jù)傳輸至工作站,用Functool2軟件進(jìn)行后處理,所有圖像經(jīng)移動(dòng)校正去除掃描過(guò)程中因受檢者頭部移動(dòng)所致的圖像配準(zhǔn)不良。采用DTIStudio2.4.01版軟件(https: //www.mristudio.org/)處理DTI數(shù)據(jù),獲得各向異性分?jǐn)?shù)(FA)圖和表面擴(kuò)散系數(shù)(ADC)圖,采用DTIStudio軟件的纖維跟蹤功能跟蹤重建腦內(nèi)白質(zhì)纖維束:起始條件為FA值>0.25的像素點(diǎn),終止條件為FA值<0.25的像素點(diǎn)或者主方向轉(zhuǎn)角>70°,以保證能跟蹤到所有可能的腦內(nèi)白質(zhì)纖維[7]。然后手工勾劃正中矢狀面上胼胝體的輪廓并根據(jù)Witelson范式分割為5個(gè)亞區(qū),同時(shí)作為感興趣區(qū)[7]。最后采用DTIStudio軟件自動(dòng)計(jì)算出總胼胝體及胼胝體5個(gè)亞區(qū)纖維束的纖維數(shù)目、長(zhǎng)度、FA值及ADC值。
2.1 兩組胼胝體纖維數(shù)目、長(zhǎng)度、FA值及ADC值比較 兩組胼胝體纖維數(shù)目、長(zhǎng)度、FA值、ADC值比較見(jiàn)表1。對(duì)照組相比,病例組總胼胝體纖維數(shù)目減少(P<0.05)、FA值下降(P<0.05)、ADC值升高(P<0.05),其胼胝體前1/3部纖維數(shù)目減少(P<0.01)、FA值下降(P<0.01)、ADC值升高(P<0.01)。兩組總胼胝體及胼胝體各部分纖維長(zhǎng)度相近(P均>0.05);兩組胼胝體前體部、后體部、峽部、壓部的纖維數(shù)目、FA值、ADC值相近(P均>0.05)。
2.2 病例組平均持續(xù)飲酒時(shí)間、日飲酒量折合純酒精與胼胝體纖維數(shù)目、FA值、ADC值的相關(guān)性 病例組平均持續(xù)飲酒時(shí)間與胼胝體前1/3部的纖維數(shù)目呈負(fù)相關(guān)(r=-0.561,P<0.05),日飲酒量折合純酒精與胼胝體前1/3部的纖維數(shù)目呈負(fù)相關(guān)(r=-0.625,P<0.05);病例組平均持續(xù)飲酒時(shí)間與胼胝體前1/3部的纖維ADC值呈正相關(guān)(r=0.657,P<0.05),日飲酒量折合純酒精與與胼胝體前1/3部的纖維ADC值呈正相關(guān)(r=0.503,P<0.05)。病例組平均持續(xù)飲酒時(shí)間、日飲酒量折合純酒精與胼胝體其余部位的纖維數(shù)目、纖維長(zhǎng)度、FA值、ADC值之間無(wú)相關(guān)關(guān)系(P均>0.05)。
表1 兩組胼胝體纖維數(shù)目、長(zhǎng)度、FA值、ADC值比較
注:與對(duì)照組相應(yīng)部位相比,*P<0.05,**P<0.01。
既往的神經(jīng)影像學(xué)及神經(jīng)病理學(xué)研究結(jié)果均提示酒精特異性腦損傷主要發(fā)生在額上回、下丘腦及小腦[8, 9]。李金鋒等[10]采用基于體素的全腦形態(tài)測(cè)量學(xué)研究發(fā)現(xiàn)酒精成癮者腦部早期變化可表現(xiàn)為局部腦灰質(zhì)、白質(zhì)結(jié)構(gòu)的萎縮,額葉灰質(zhì)及白質(zhì)是酒精性腦損傷相對(duì)特異的腦區(qū)。趙珊珊等[11]測(cè)量慢性酒精中毒患者額葉白質(zhì)、半卵圓中心、胼胝體膝部、壓部、丘腦等5個(gè)感興趣區(qū)的FA值,結(jié)果顯示慢性酒精中毒患者存在胼胝體膝部、壓部、半卵圓中心和額葉白質(zhì)纖維的異常。國(guó)外一項(xiàng)功能磁共振成像研究表明酒依賴患者的認(rèn)知功能損害與腦白質(zhì)連通性異常存在相關(guān)性[12]。
腦白質(zhì)纖維跟蹤技術(shù)是近年來(lái)磁共振成像技術(shù)的一項(xiàng)重大進(jìn)展,它是利用彌散張量數(shù)據(jù),在活體上三維顯示腦白質(zhì)纖維束的一種無(wú)創(chuàng)性成像方法。由于該技術(shù)具有真實(shí)、客觀顯示神經(jīng)纖維束走向和分布的能力,將有助于理解正常腦功能和多種影響腦功能的病理過(guò)程[7]。胼胝體是連接兩側(cè)大腦半球新皮層的主要聯(lián)絡(luò)纖維,胼胝體前1/3部聯(lián)絡(luò)著雙側(cè)前額葉纖維;胼胝體前體部纖維主要聯(lián)系雙側(cè)額葉的運(yùn)動(dòng)前區(qū)和中央前回,后體部纖維聯(lián)系雙側(cè)頂葉;峽部聯(lián)系雙側(cè)顳葉;胼胝體壓部纖維聯(lián)系雙側(cè)枕葉。作為人腦中最大的神經(jīng)通路,胼胝體與大腦半球之間的信息傳送密切相關(guān),纖維投射至各個(gè)功能腦區(qū),共同參與了感覺(jué)、記憶、學(xué)習(xí)和運(yùn)動(dòng)等功能活動(dòng)[13]。以胼胝體為研究對(duì)象能直觀觀察到腦內(nèi)各神經(jīng)解剖結(jié)構(gòu)與白質(zhì)纖維束的關(guān)系。
本研究發(fā)現(xiàn),與對(duì)照相比,病例組總胼胝體與胼胝體前1/3部的纖維數(shù)目下降、FA值下降、ADC值升高,且胼胝體前1/3部的纖維損害與飲酒持續(xù)時(shí)間、飲酒量密切相關(guān)。FA值的下降、ADC值的升高反映了軸突密度、髓鞘形成的下降及大腦軸突組織的異常。提示酒依賴患者雙側(cè)大腦纖維連接異常,尤其是前額葉纖維受累明顯。Pfefferbaum等[5]采用纖維跟蹤技術(shù)定量分析了87例酒依賴患者的胼胝體纖維,發(fā)現(xiàn)除了前體部纖維外,其他各部胼胝體纖維均存在異常,且與患者的精神運(yùn)動(dòng)功能、平衡功能損害相關(guān)。Willi等[14]的研究發(fā)現(xiàn)可卡因?yàn)E用患者存在額葉-顳葉、額葉-丘腦以及胼胝體白質(zhì)纖維束異常,且研究者認(rèn)為該通路的異??赡苁俏镔|(zhì)濫用者共同的病理生理學(xué)基礎(chǔ)。
值得指出的是,本研究所采用的“纖維數(shù)目”并非指真正意義上的纖維數(shù)目,該指標(biāo)的大小與纖維跟蹤時(shí)設(shè)定的跟蹤起始條件及終止條件有關(guān),如設(shè)定的跟蹤起始及終止條件中FA的閾值越低、轉(zhuǎn)角越小,得出的纖維數(shù)目越多,也越容易得到一些實(shí)際上不存在的纖維連接。故本研究采用Mori等[15]描述的標(biāo)準(zhǔn)閾值,使得結(jié)果更可信,更具有可重復(fù)性。
本研究通過(guò)基于DTI的纖維跟蹤技術(shù)測(cè)量跟蹤出的胼胝體纖維的各個(gè)指標(biāo),是評(píng)價(jià)胼胝體纖維連通性最為直接有效指標(biāo)。但纖維跟蹤技術(shù)本身仍然存在一些局限性,如部分容積效應(yīng)會(huì)影響到纖維跟蹤的結(jié)果,當(dāng)不同纖維束在同一體素內(nèi)交叉、緊貼、分叉或融合時(shí),將難以反映纖維的真正軌跡;同時(shí),噪聲、偽影等也可對(duì)纖維跟蹤產(chǎn)生不利的影響[16, 17]。采用更為先進(jìn)的纖維跟蹤技術(shù)進(jìn)行大樣本的胼胝體纖維跟蹤研究是有必要的。
[1] 杜好瑞,穆俊林,張寧,等.男性酒依賴患者執(zhí)行功能與事件相關(guān)電位P300研究[J].中國(guó)神經(jīng)精神疾病雜志,2015,41(2):102-105.
[2] 徐亞輝,王瑛,劉暉,等.酒依賴患者神經(jīng)肽Y與焦慮、抑郁及渴求的相關(guān)性[J].中國(guó)神經(jīng)精神疾病雜志,2015,41(11):690-693.
[3] Pfefferbaum A, Rosenbloom MJ, Chu W, et al. White matter microstructural recovery with abstinence and decline with relapse in alcohol dependence interacts with normal ageing: a controlled longitudinal DTI study[J]. Lancet Psychiatry, 2014,1(3):202-212.
[4] Trivedi R, Bagga D, Bhattacharya D, et al. White matter damage is associated with memory decline in chronic alcoholics: a quantitative diffusion tensor tractography study[J]. Behav Brain Res, 2013,250(6):192-198.
[5] Pfefferbaum A, Rosenbloom MJ, Fama R, et al. Transcallosal white matter degradation detected with quantitative fiber tracking in alcoholic men and women: selective relations to dissociable functions[J] . Alcohol Clin Exp Res, 2010,34(7):1201-1211.
[6] Sacanella E, Fernández-Solà J, Cofan M, et al. Chronic alcoholic myopathy: diagnostic clues and relationship with other ethanol-related diseases[J]. QJM, 1995,88(11):811-817.
[7] 儲(chǔ)康康,洪珊珊,柯曉燕,等.高功能孤獨(dú)障礙患兒胼胝體和額葉纖維的對(duì)照研究[J].中華精神科雜志,2010,43(3):156-160.
[8] Mechtcheriakov S, Brenneis C, Egger K, et al. A widespread distinct pattern of cerebral atrophy in patients with alcohol addiction revealed by voxel-based morphometry[J]. J Neurol Neurosurg Psychiatry, 2007,78(6):610-614.
[9] Harper C. The neuropathology of alcohol-specific brain damage, or does alcohol damage the brain[J]. J Neuropathol Exp Neurol, 1998,57(2):101-110.
[10] 李金鋒,陳志曄,馬林.酒精成癮者的體素全腦形態(tài)測(cè)量學(xué)分析[J].中華放射學(xué)雜志,2011,45(9):827-830.
[11] 趙珊珊,甘萬(wàn)崇,陳軍,等.磁共振擴(kuò)散張量成像在慢性酒精中毒性腦病的初步臨床應(yīng)用[J].武漢大學(xué)學(xué)報(bào)(醫(yī)學(xué)版),2008,29(2):235-238.
[12] Jansen JM, van Holst RJ, van den Brink W, et al. Brain function during cognitive flexibility and white matter integrity in alcohol-dependent patients, problematic drinkers and healthy controls[J]. Addict Biol, 2015,20(5):979-989.
[13] Paul LK, Brown WS, Adolphs R, et al. Agenesis of the corpus callosum: genetic, developmental and functional aspects of connectivity[J]. Nat Rev Neurosci, 2007,8(4):287-299.
[14] Willi TS, Barr AM, Gicas K, et al. Characterization of white matter integrity deficits in cocaine-dependent individuals with substance-induced psychosis compared with non-psychotic cocaine users[J]. Addict Biol, 2016. doi: 10.1111/adb.12363. [Epub ahead of print]
[15] Mori S, Crain BJ, Chacko VP, et al. Three-dimensional tracking of axonal projections in the brain by magnetic resonance imaging[J]. Ann Neurol, 1999,45(2):265-269.
[16] Poupon C, Mangin J, Clark CA, et al. Towards inference of human brain connectivity from MR diffusion tensor data[J]. Med Image Anal, 2001,5(1):1-15.
[17] Cabeen RP, Bastin ME, Laidlaw DH. Kernel regression estimation of fiber orientation mixtures in diffusion MRI[J]. Neuroimage, 2016,127(15):158-172.
HONGShanshan1,ZHAOZhong,HANBojun,WANGQingguang,JIANGQitao,
ZHENYongqiang,LIUDinghua
(1SoochowHospitalAffiliatedtoNanjingMedicalUniversity,Suzhou215001,China)
Objective To observe the changes in fiber number and structure of corpus callosum in patients with alcohol dependence through fiber tractography of magnetic resonance diffusion tensor imaging.Methods T1-weighted magnetic resonance imaging and diffusion tensor imaging were obtained from 48 alcohol-dependent patients (observation group) and 50 cases of age, sex, education year-matched normal controls (control group). The fiber number, fiber fractional anisotropy (FA), and fiber apparent diffusion coefficient (ADC) of the corpus callosum between the two groups were calculated. Results The fiber number of total corpus callosum in the observation group was 2587±654, which was 2875±758 in the control group, and significant difference was found between these two groups (P<0.05). The fiber number in anterior one third of corpus callosum in the observation group was 782±254, which was 987±244 in the control group, there was significant difference between the two groups (P<0.01). The FA values of total corpus callosum in the observation group were 0.61±0.02, which were significantly decreased as compared with than that (0.62±0.02) of the control group (P<0.05). FA values of anterior one third of corpus callosum in the observation group (0.59±0.03) were decreased as compared with that (0.61±0.03) of the control group (P<0.01). Compared with the control group [(0.91±0.07) ×10-3mm2/s], the ADC values of total corpus callosum in the observation group [(0.94±0.07) ×10-3mm2/s] were significantly increased (P<0.05). The ADC values of anterior one third of corpus callosum in the observation group [(0.94±0.06) ×10-3mm2/s] were increased as compared with that [(0.87±0.08) ×10-3mm2/s] of the control group (P<0.01). Conclusion Fiber number and structure of the corpus callosum is abnormal in alcohol-dependent patients and this anomaly in the anterior one third of corpus callosum is more obvious.
alcohol dependence; corpus callosum; fiber of corpus callosum; magnetic resonance imaging; diffusion tensor imaging; fiber tractography
江蘇省蘇州市科技發(fā)展計(jì)劃項(xiàng)目(SYS201426)。
洪珊珊(1983-),女,碩士,主治醫(yī)師,主要研究方向?yàn)樯窠?jīng)影像學(xué)。E-mail: 13914190005@163.com
簡(jiǎn)介:趙中(1963-),男,碩士,主任醫(yī)師,主要研究方向?yàn)樯窠?jīng)影像學(xué)。E-mail: zhaozhong1963@sina.com
10.3969/j.issn.1002-266X.2016.43.004
R741.02
A
1002-266X(2016)43-0011-04
2016-07-15)