Share:
Share this content in WeChat
X
Clinical Articles
Cerebral blood flow perfusion characteristics in preterm infants with bronchopulmonary dysplasia based on 3D-ASL and its correlation with duration of mechanical ventilation
WANG Ning  LI Xinqi  CHENG Zhiwei  FU Yiwei  DING Tan  LIU Xueyan  LI Tianyu  WANG Kefan  LU Lin 

Cite this article as WANG N, LI X Q, CHENG Z W, et al. Cerebral blood flow perfusion characteristics in preterm infants with bronchopulmonary dysplasia based on 3D-ASL and its correlation with duration of mechanical ventilation[J]. Chin J Magn Reson Imaging, 2026, 17(8): 64-70, 97. DOI:10.12015/issn.1674-8034.2026.08.006.


[Abstract] Objective Using three-dimensional arterial spin labeling (3D-ASL) technology to investigate cerebral blood flow perfusion characteristics and their correlation with mechanical ventilation duration in preterm infants with bronchopulmonary dysplasia (BPD).Materials and Methods A total of 122 preterm infants who were hospitalized in the Neonatal Intensive Care Unit of the Third Affiliated Hospital of Zhengzhou University from January 2024 to September 2024 and underwent magnetic resonance imaging (MRI) examination in the Department of Radiology were prospectively and consecutively enrolled as study subjects. According to the diagnostic criteria for BPD, the patients were divided into a BPD group (n = 61) and a control group (n = 61). All subjects underwent conventional cranial MRI sequences and ASL sequence scanning at a corrected gestational age of 35 to 39 weeks. Cerebral blood flow (CBF) values were quantitatively measured in regions of interest, including the bilateral frontal, parietal, temporal, and occipital cortices and white matter, basal ganglia, and thalamus. Clinical data and CBF values were compared between the two groups. The effect of sex on CBF in the BPD group was analyzed, and partial correlation and subgroup-stratified analyses were performed within the BPD group to explore the correlation between CBF in the brain regions showing significant intergroup differences and the duration of mechanical ventilation.Results The duration of mechanical ventilation, invasive ventilation, and non-invasive ventilation in the BPD group was longer than that in the control group (P < 0.05). Compared with the control group, the CBF values in the bilateral frontal cortex, bilateral parietal cortex, bilateral temporal cortex, bilateral occipital cortex, right frontal white matter, left parietal white matter, bilateral temporal white matter, right occipital white matter, bilateral basal ganglia and bilateral thalamus of the BPD group increased (P < 0.05). Gender had no significant effect on CBF levels in various brain regions of preterm infants with BPD (P > 0.05). In the overall BPD group (corrected gestational age 35~38 weeks), there was no significant correlation between CBF in the brain regions showing significant intergroup differences and the duration of mechanical ventilation (P > 0.05); stratified analysis showed that in the subgroup with a corrected gestational age of 37 to 38 weeks, CBF in the left parietal white matter (r = 0.421, P = 0.040) and right occipital white matter (r = 0.476, P = 0.019) was significantly positively correlated with the duration of mechanical ventilation.Conclusions 3D-ASL can reveal CBF perfusion abnormalities in preterm infants with BPD. In preterm infants with BPD at corrected gestational age of 37 to 38 weeks, there is a positive correlation between left parietal white matter and right occipital white matter CBF and mechanical ventilation duration. Clinical attention should be paid to the blood flow changes in the aforementioned brain regions of children undergoing long-term mechanical ventilation, optimizing respiratory support strategies, and strengthening neurodevelopmental follow-up.
[Keywords] bronchopulmonary dysplasia;preterm infants;magnetic resonance imaging;arterial spin labeling;cerebral blood flow;mechanical ventilation

WANG Ning1   LI Xinqi1   CHENG Zhiwei2   FU Yiwei1   DING Tan1   LIU Xueyan1   LI Tianyu1   WANG Kefan1   LU Lin1*  

1 Department of Medical Imaging, the Third Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China

2 Department of Medical Records Management, the Third Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China

Corresponding author: LU L, E-mail: lulin3186@126.com

Conflicts of interest   None.

Received  2026-03-31
Accepted  2026-07-14
DOI: 10.12015/issn.1674-8034.2026.08.006
Cite this article as WANG N, LI X Q, CHENG Z W, et al. Cerebral blood flow perfusion characteristics in preterm infants with bronchopulmonary dysplasia based on 3D-ASL and its correlation with duration of mechanical ventilation[J]. Chin J Magn Reson Imaging, 2026, 17(8): 64-70, 97. DOI:10.12015/issn.1674-8034.2026.08.006.

[1]
AMBALAVANAN N, DEUTSCH G, PRYHUBER G, et al. The evolving pathophysiology of bronchopulmonary dysplasia[J]. Physiol Rev, 2026, 106(1): 197-237. DOI: 10.1152/physrev.00042.2024.
[2]
VARGHESE N P, ALTIT G, GUBICHUK M M, et al. Navigating diagnostic and treatment challenges of pulmonary hypertension in infants with bronchopulmonary dysplasia[J/OL]. J Clin Med, 2024, 13(12): 3417 [2026-03-30]. https://pubmed.ncbi.nlm.nih.gov/38929946/. DOI: 10.3390/jcm13123417.
[3]
LÖFBERG L, ABRAHAMSSON T, BJÖRKLUND L J, et al. Respiratory support and bronchopulmonary dysplasia in infants born at 22-26 weeks gestation in Sweden, 2004-2007 and 2014-2016[J/OL]. Eur Respir J, 2025, 65(1): 2401203 [2026-03-30]. https://pubmed.ncbi.nlm.nih.gov/39510555/. DOI: 10.1183/13993003.01203-2024.
[4]
JEON G W, OH M, CHANG Y S. Increased bronchopulmonary dysplasia along with decreased mortality in extremely preterm infants[J/OL]. Sci Rep, 2025, 15: 8720 [2026-03-30]. https://pubmed.ncbi.nlm.nih.gov/40082666/. DOI: 10.1038/s41598-025-93466-8.
[5]
MOREIRA A, NORONHA M, JOY J, et al. Rates of bronchopulmonary dysplasia in very low birth weight neonates: a systematic review and meta-analysis[J/OL]. Respir Res, 2024, 25(1): 219 [2026-03-30]. https://pubmed.ncbi.nlm.nih.gov/38790002/. DOI: 10.1186/s12931-024-02850-x.
[6]
MARTIN M, SMITH L, HOFHEIMER J A, et al. Bronchopulmonary dysplasia and neurobehavioural outcomes at birth and 2 years in infants born before 30 weeks[J]. Arch Dis Child Fetal Neonatal Ed, 2023, 108(2): 142-148. DOI: 10.1136/archdischild-2021-323405.
[7]
TRÉLUYER L, NUYTTEN A, GUELLEC I, et al. Neurodevelopment and healthcare utilisation at age 5-6 years in bronchopulmonary dysplasia: an EPIPAGE-2 cohort study[J]. Arch Dis Child Fetal Neonatal Ed, 2023, 109(1): 26-33. DOI: 10.1136/archdischild-2023-325376.
[8]
EVES R, MENDONÇA M, BAUMANN N, et al. Association of very preterm birth or very low birth weight with intelligence in adulthood: an individual participant data meta-analysis[J/OL]. JAMA Pediatr, 2021, 175(8): e211058 [2026-03-30]. https://pubmed.ncbi.nlm.nih.gov/34047752/. DOI: 10.1001/jamapediatrics.2021.1058.
[9]
KIM H G, CHOI J W, LEE J H, et al. Association of cerebral blood flow and brain tissue relaxation time with neurodevelopmental outcomes of preterm neonates: multidelay arterial spin labeling and synthetic MRI study[J]. Invest Radiol, 2022, 57(4): 254-262. DOI: 10.1097/RLI.0000000000000833.
[10]
OUYANG M H, DETRE J A, HYLAND J L, et al. Spatiotemporal cerebral blood flow dynamics underlies emergence of the limbic-sensorimotor-association cortical gradient in human infancy[J/OL]. Nat Commun, 2024, 15: 8944 [2026-03-30]. https://pubmed.ncbi.nlm.nih.gov/39414859/. DOI: 10.1038/s41467-024-53354-7.
[11]
HU X Q, SONG R, DASGUPTA C, et al. Fetal hypoxia suppresses TRPC6 and impairs cerebral autoregulation in neonatal rats[J]. Stroke, 2025, 56(12): 3454-3467. DOI: 10.1161/STROKEAHA.125.052524.
[12]
GLASER K, JENSEN E A, WRIGHT C J. Prevention of inflammatory disorders in the preterm neonate: an update with a special focus on bronchopulmonary dysplasia[J]. Neonatology, 2024, 121(5): 636-645. DOI: 10.1159/000539303.
[13]
TORTORA D, SEVERINO M, ROSSI A. Arterial spin labeling perfusion in neonates[J/OL]. Semin Fetal Neonatal Med, 2020, 25(5): 101130 [2026-03-30]. https://pubmed.ncbi.nlm.nih.gov/32591228/. DOI: 10.1016/j.siny.2020.101130.
[14]
FU Y W, DING D, QIN C, et al. Application of 3D-pCASL in evaluating cerebral perfusion and early prognosis in extremely preterm infants with HIBD[J]. Chin J Magn Reson Imaging, 2025, 16(11): 49-55, 63. DOI: 10.12015/issn.1674-8034.2025.11.007.
[15]
DING D, FU Y W, LI S K, et al. Association between gestational diabetes mellitus and brain development in very preterm infants: a quantitative 3D-ASL study[J]. Chin J Magn Reson Imaging, 2026, 17(1): 1-7, 28. DOI: 10.12015/issn.1674-8034.2026.01.001.
[16]
HIJMAN A S, WEHRLE F M, LATAL B, et al. Cerebral perfusion differences are linked to executive function performance in very preterm-born children and adolescents[J/OL]. Neuroimage, 2024, 285: 120500 [2026-03-30]. https://pubmed.ncbi.nlm.nih.gov/38135171/. DOI: 10.1016/j.neuroimage.2023.120500.
[17]
CIRILLO M, PUZONE S, DE ROSA A P, et al. ASL reveals regional brain perfusion impairment in neonates with mild hypoxic ischemic encephalopathy[J/OL]. Sci Rep, 2025, 15: 31676 [2026-03-30]. https://pubmed.ncbi.nlm.nih.gov/40866485/. DOI: 10.1038/s41598-025-17246-0.
[18]
GEORGOPOULOS D, TARAN S, BOLAKI M, et al. Mechanical ventilation in patients with acute brain injuries: a pathophysiology-based approach[J]. Am J Respir Crit Care Med, 2025, 211(6): 932-945. DOI: 10.1164/rccm.202409-1813SO.
[19]
SHARIE S AL, ALMARI R, AZZAM S, et al. Brain protective ventilation strategies in severe acute brain injury[J/OL]. Curr Neurol Neurosci Rep, 2025, 25: 68 [2026-03-30]. https://pubmed.ncbi.nlm.nih.gov/41082009/. DOI: 10.1007/s11910-025-01462-2.
[20]
ZHANG C, LI W L, LU L, et al. Influence of bronchopulmonary dysplasia on cerebral blood flow in preterm infants: a prospective study based on arterial spin labeling[J]. Chin J Contemp Pediatr, 2023, 25(1): 31-37. DOI: 10.7499/j.issn.1008-8830.2208068.
[21]
Chinese Medical Association Neonatology Branch, Beijing Medical Association Neonatology Branch, LI Q P, et al. Expert consensus on prevention of intraventricular hemorrhage in preterm infants(2025) [J/OL]. Chin J Obstet Gynecol Pediatr Electron Ed, 2025, 21(1): 1-14. DOI: 10.3877/cma.j.issn.1673-5250.2025.01.001.
[22]
HIGGINS R D, JOBE A H, KOSO-THOMAS M, et al. Bronchopulmonary dysplasia: executive summary of a workshop[J/OL]. J Pediatr, 2018, 197: 300-308 [2026-03-30]. https://pubmed.ncbi.nlm.nih.gov/29551318/. DOI: 10.1016/j.jpeds.2018.01.043.
[23]
KIM C, UFKES S, GUO T, et al. Associations of bronchopulmonary dysplasia and infection with school-age brain development in children born preterm[J/OL]. J Pediatr, 2025, 281: 114524 [2026-03-30]. https://pubmed.ncbi.nlm.nih.gov/41389653/. DOI: 10.1016/j.jpeds.2025.114524.
[24]
SHIMOTSUMA T, TOMOTAKI S, AKITA M, et al. Severe bronchopulmonary dysplasia adversely affects brain growth in preterm infants[J]. Neonatology, 2024, 121(6): 724-732. DOI: 10.1159/000538527.
[25]
MUKERJI A, READ B, SU Y C, et al. Severity of bronchopulmonary dysplasia using a contemporary Canadian definition and early childhood outcomes: a population-based cohort study[J/OL]. J Pediatr, 2025, 287: 114763 [2026-03-30]. https://pubmed.ncbi.nlm.nih.gov/40783050/. DOI: 10.1016/j.jpeds.2025.114763.
[26]
KLINE J E, ILLAPANI V S P, HE L L, et al. Retinopathy of prematurity and bronchopulmonary dysplasia are independent antecedents of cortical maturational abnormalities in very preterm infants[J/OL]. Sci Rep, 2019, 9: 19679 [2026-03-30]. https://pubmed.ncbi.nlm.nih.gov/31873183/. DOI: 10.1038/s41598-019-56298-x.
[27]
LEE J M, CHOI Y H, 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. DOI: 10.1159/000499487.
[28]
PETERSON B S, DELAVARI S, SADIK J, et al. Brain tissue microstructure in a prospective, longitudinal, population-based cohort of preterm and term-born young adults[J]. J Child Psychol Psychiatry, 2025, 66(5): 635-649. DOI: 10.1111/jcpp.14069.
[29]
WANG Y J, LIU S S, LIU Y C, et al. An assessment of white matter development in preterm infants with bronchopulmonary dysplasia using diffusion tensor imaging[J]. Chin J Contemp Pediatr, 2020, 22(10): 1079-1084. DOI: 10.7499/j.issn.1008-8830.2004236.
[30]
BASU S K, KAPSE K J, MURNICK J, et al. Impact of bronchopulmonary dysplasia on brain GABA concentrations in preterm infants: Prospective cohort study[J/OL]. Early Hum Dev, 2023, 186: 105860 [2026-03-30]. https://pubmed.ncbi.nlm.nih.gov/37757548/. DOI: 10.1016/j.earlhumdev.2023.105860.
[31]
BARNES E A, KNUTSEN C, KINDT A, et al. Hypoxia-inducible factor-1α in SM22α-expressing cells modulates alveolarization[J]. Am J Respir Cell Mol Biol, 2023, 69(4): 470-483. DOI: 10.1165/rcmb.2023-0045OC.
[32]
GONZALEZ M, CLAYTON S, WAUSON E, et al. Promotion of nitric oxide production: mechanisms, strategies, and possibilities[J/OL]. Front Physiol, 2025, 16: 1545044 [2026-03-30]. https://pubmed.ncbi.nlm.nih.gov/39917079/. DOI: 10.3389/fphys.2025.1545044.
[33]
KANAAN A, FARAHANI R, DOUGLAS R M, et al. Effect of chronic continuous or intermittent hypoxia and reoxygenation on cerebral capillary density and myelination[J/OL]. Am J Physiol Regul Integr Comp Physiol, 2006, 290(4): R1105-R1114 [2026-03-30]. https://pubmed.ncbi.nlm.nih.gov/16322350/. DOI: 10.1152/ajpregu.00535.2005.
[34]
THÉBAUD B, GOSS K N, LAUGHON M, et al. Bronchopulmonary dysplasia[J/OL]. Nat Rev Dis Primers, 2019, 5: 78 [2026-03-30]. https://pubmed.ncbi.nlm.nih.gov/31727986/. DOI: 10.1038/s41572-019-0127-7.
[35]
ALVAREZ-FUENTE M, MORENO L, LOPEZ-ORTEGO P, et al. Exploring clinical, echocardiographic and molecular biomarkers to predict bronchopulmonary dysplasia[J/OL]. PLoS One, 2019, 14(3): e0213210 [2026-03-30]. https://pubmed.ncbi.nlm.nih.gov/30840669/. DOI: 10.1371/journal.pone.0213210.
[36]
ASHBY J W, MACK J J. Endothelial control of cerebral blood flow[J]. Am J Pathol, 2021, 191(11): 1906-1916. DOI: 10.1016/j.ajpath.2021.02.023.
[37]
CLAASSEN J A H R, THIJSSEN D H J, PANERAI R B, et al. Regulation of cerebral blood flow in humans: physiology and clinical implications of autoregulation[J]. Physiol Rev, 2021, 101(4): 1487-1559. DOI: 10.1152/physrev.00022.2020.
[38]
LEARY S, DAS P, PONNALAGU D, et al. Genetic strain and sex differences in a hyperoxia-induced mouse model of varying severity of bronchopulmonary dysplasia[J]. Am J Pathol, 2019, 189(5): 999-1014. DOI: 10.1016/j.ajpath.2019.01.014.
[39]
GUILLOT M, GUO T, UFKES S, et al. Mechanical ventilation duration, brainstem development, and neurodevelopment in children born preterm: a prospective cohort study[J/OL]. J Pediatr, 2020, 226: 87-95.e3 [2026-03-30]. https://pubmed.ncbi.nlm.nih.gov/32454115/. DOI: 10.1016/j.jpeds.2020.05.039.
[40]
LAHR B E, BRUNSCH C L, DIKKERS R, et al. Cerebrovascular autoregulation in preterm infants using heart rate or blood pressure: a pilot study[J/OL]. Children (Basel), 2024, 11(7): 765 [2026-03-30]. https://pubmed.ncbi.nlm.nih.gov/39062215/. DOI: 10.3390/children11070765.

PREV Evaluation of white matter microstructural impairment in temporal lobe epilepsy using peak width of skeletonized mean diffusivity
NEXT Predictive value of DTI-ALPS combined with FA and standard MRI quantitative parameters for IDH mutation in adult-type diffuse high-grade gliomas
  



Tel & Fax: +8610-67113815    E-mail: editor@cjmri.cn