
应用弥散张量成像评价支气管肺发育不良早产儿脑白质发育的研究
王银娟, 刘沙沙, 刘彦超, 李潇男, 张瑞丽, 徐发林
中国当代儿科杂志 ›› 2020, Vol. 22 ›› Issue (10) : 1079-1084.
应用弥散张量成像评价支气管肺发育不良早产儿脑白质发育的研究
An assessment of white matter development in preterm infants with bronchopulmonary dysplasia using diffusion tensor imaging
目的 应用磁共振弥散张量成像(DTI)的各项异性分数(FA)和表观弥散系数(ADC)评价支气管肺发育不良(BPD)早产儿的脑白质发育。方法 以2016年8月至2019年4月生后24 h内收住NICU的出生胎龄≤32周、出生体重<1 500 g,且出院前完成头颅MRI及DTI检查的96例早产儿为研究对象。根据出院诊断分为BPD组(n=48)和非BPD组(n=48),比较两组DTI相同感兴趣区的FA值和ADC值。结果 两组早产儿脑室周围-脑室内出血、脑室周围白质软化、局灶性脑白质损伤等发生率差异无统计学意义(P > 0.05)。BPD组早产儿内囊后肢、胼胝体压部、枕叶白质、小脑、大脑脚的FA值低于非BPD组(P < 0.05),各ADC值高于非BPD组(P < 0.05)。与非BPD组相比,BPD组早产儿呼吸暂停次数更多、肺炎发生率和机械通气比例更高、辅助通气时间更长(P < 0.05)。结论 BPD对早产儿脑白质发育具有潜在影响,可导致脑白质发育延迟,因此,需关注该类患儿的神经功能。
Objective To assess white matter development in preterm infants with bronchopulmonary dysplasia (BPD) using fractional anisotropy (FA) and apparent diffusion coefficient (ADC) values of diffusion tensor imaging (DTI). Methods Ninety-six infants with a gestational age of ≤ 32 weeks and a birth weight of < 1 500 g who were admitted to the neonatal intensive care unit within 24 hours after birth from August 2016 to April 2019 and underwent head MRI and DTI before discharge were enrolled. According to the discharge diagnosis, they were divided into BPD group with 48 infants and non-BPD group with 48 infants. The two groups were compared in terms of FA and ADC values of the same regions of interest on DTI image. Results There were no significant differences in the incidence rates of periventricular/intraventricular hemorrhage, periventricular leukomalacia, and punctate white matter lesions between the two groups (P > 0.05). Compared with the non-BPD group, the BPD group had significantly lower FA values and significantly higher ADC values of the posterior limb of the internal capsule, the splenium of the corpus callosum, the occipital white matter, the cerebellum, and the cerebral peduncle (P < 0.05). Compared with the non-BPD group, the BPD group had a significantly higher frequency of apnea, a significantly higher proportion of infants with pneumonia or mechanical ventilation, and a significantly longer duration of assisted ventilation (P < 0.05). Conclusions BPD may has potential adverse effects to white matter development in preterm infants, leading to delayed white matter development. Therefore, it is necessary to pay attention to the neurological function of these infants.
支气管肺发育不良 / 脑白质发育 / 弥散张量成像 / 各项异性分数 / 表观弥散系数 / 早产儿
Bronchopulmonary dysplasia / White matter development / Diffusion tensor imaging / Fractional anisotropy / Apparent diffusion coefficient / Preterm infant
[1] Stoll BJ, Hansen NI, Bell EF, et al. Trends in care practices, morbidity, and mortality of extremely preterm neonates, 1993-2012[J]. JAMA, 2015, 314(10):1039-1051.
[2] Guaman MC, Gien J, Baker CD, et al. Point prevalence, clinical characteristics, and treatment variation for infants with severe bronchopulmonary dysplasia[J]. Am J Perinatol, 2015, 32(10):960-967.
[3] Viscardi RM. Perinatal inflammation and lung injury[J]. Semin Fetal Neonatal Med, 2012, 17(1):30-35.
[4] Trittmann JK, Nelin LD, Klebanoff MA. Bronchopulmonary dysplasia and neurodevelopmental outcome in extremely preterm neonates[J]. Eur J Pediatr, 2013, 172(9):1173-1180.
[5] Lin F, Dong H, Song Y, et al. Effect of bronchopulmonary dysplasia on early intellectual development in preterm infants[J]. Pediatr Int, 2017, 59(6):691-697.
[6] 林颖仪, 黄水清. 早产儿脑损伤影像学及脑电图诊断的研究进展[J]. 临床儿科杂志, 2017, 35(7):548-552.
[7] 张浩然, 黄海云. 早产儿脑损伤的早期评估研究进展[J]. 国际儿科学杂志, 2018, 45(1):28-31.
[8] Schneider J, Kober T, Bickle Graz M, et al. Evolution of T1 relaxation, ADC, and fractional anisotropy during early brain maturation:a serial imaging study on preterm infants[J]. AJNR Am J Neuroradiol, 2016, 37(1):155-162.
[9] Jensen EA, Dysart K, Gantz MG, et al. The diagnosis of bronchopulmonary dysplasia in very preterm infants. an evidence-based approach[J]. Am J Respir Crit Care Med, 2019, 200(6):751-759.
[10] Zulqarnain A, Hussain M, Suleri KM, et al. Comparison of caffeine versus theophylline for apnea of prematurity[J]. Pak J Med Sci, 2019, 35(1):113-116.
[11] 中华医学会儿科学分会新生儿学组, 中国医师协会新生儿科医师分会感染专业委员会. 新生儿败血症诊断及治疗专家共识(2019年版)[J]. 中华儿科杂志, 2019, 57(4):252-257.
[12] 邵肖梅, 叶鸿瑁, 丘小汕. 实用新生儿学[M]. 第5版. 北京:人民卫生出版社, 2019:368-370, 582-588, 632-639, 1025-1029.
[13] 王飞, 刘亚辉, 黄婷婷. PVL脑瘫患儿MRI分级与粗大运动功能分级的相关性分析[J]. 医学影像学杂志, 2019, 29(5):721-725.
[14] Wagenaar N, Chau V, Groenendaal F, et al. Clinical risk factors for punctate white matter lesions on early magnetic resonance imaging in preterm newborns[J]. J Pediatr, 2017, 182:34-40.e1.
[15] Sie LT, van der Knaap MS, van Wezel-Meijler G, et al. Early MR features of hypoxic-ischemic brain injury in neonates with periventricular densities on sonograms[J]. AJNR Am J Neuroradiol, 2000, 21(5):852-861.
[16] Keeney SE, Adcock EW, Mcardle CB. Prospective observations of 100 high-risk neonates by high-field (1.5 Tesla) magnetic resonance imaging of the central nervous system:I. Intraventricular and extracerebral lesions[J]. Pediatrics, 1991, 87(4):421-430.
[17] Papile LA, Burstein J, Burstein R, et al. Incidence and evolution of subependymal and intraventricular hemorrhage:a study of infants with birth weights less than 1,500 gm[J]. J Pediatr, 1978, 92(4):529-534.
[18] Gagliardi L, Bellù R, Zanini R, et al. Bronchopulmonary dysplasia and brain white matter damage in the preterm infant:a complex relationship[J]. Paediatr Perinat Epidemiol, 2009, 23(6):582-590.
[19] Natarajan G, Pappas A, Shankaran S, et al. Outcomes of extremely low birth weight infants with bronchopulmonary dysplasia:impact of the physiologic definition[J]. Early Hum Dev, 2012, 88(7):509-515.
[20] van Pul C, Buijs J, Janssen MJ, et al. Selecting the best index for following the temporal evolution of apparent diffusion coefficient and diffusion anisotropy after hypoxic-ischemic white matter injury in neonates[J]. AJNR Am J Neuroradiol, 2005, 26(3):469-481.
[21] Pieterman K, Plaisier A, Govaert P, et al. Data quality in diffusion tensor imaging studies of the preterm brain:a systematic review[J]. Pediatr Radiol, 2015, 45(9):1372-1381.
[22] Lee JM, Choi YH, Hong J, et al. Bronchopulmonary dysplasia is associated with altered brain volumes and white matter microstructure in preterm infants[J]. Neonatology, 2019, 116(2):163-170.
[23] Boardman JP, Counsell SJ, Rueckert D, et al. Early growth in brain volume is preserved in the majority of preterm infants[J]. Ann Neurol, 2007, 62(2):185-192.
[24] Thompson DK, Warfield SK, Carlin JB, et al. Perinatal risk factors altering regional brain structure in the preterm infant[J]. Brain, 2007, 130(Pt 3):667-677.
[25] Anjari M, Counsell SJ, Srinivasan L, et al. The association of lung disease with cerebral white matter abnormalities in preterm infants[J]. Pediatrics, 2009, 124(1):268-276.
[26] Durand M, Mcevoy C, Macdonald K. Spontaneous desaturations in intubated very low birth weight infants with acute and chronic lung disease[J]. Pediatr Pulmonol, 1992, 13(3):136-142.
[27] 李文丽, 徐发林, 牛铭, 等. 不同程度支气管肺发育不良早产儿的临床特征及预后分析[J]. 中国当代儿科杂志, 2018, 20(4):261-266.