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1.
Vaccine ; 42(9): 2135-2137, 2024 Apr 02.
Article in English | MEDLINE | ID: mdl-38453618

ABSTRACT

The COVID-19 pandemic has affected people of all ages worldwide. However, there is still no information on the vaccine effectiveness (VE) of inactivated COVID-19 vaccines in children aged less than 3 years old. This study highlighted that 2 doses of CoronaVac were effective in preventing COVID-19, with a VE of 83.1 %.


Subject(s)
COVID-19 Vaccines , COVID-19 , Vaccines, Inactivated , Child , Humans , Child, Preschool , COVID-19/prevention & control , Hong Kong/epidemiology , Pandemics
3.
Public Health ; 226: 80-83, 2024 Jan.
Article in English | MEDLINE | ID: mdl-38016199

ABSTRACT

OBJECTIVE: This study is to evaluate if there is any difference in the balance between incidence of and remission from overweight/obesity in Hong Kong school-age children before and during the COVID-19 pandemic over three years. METHODS: This is a retrospective longitudinal study that involved children aged 6-16 years from a database of the School Physical Fitness Award Scheme. RESULTS: 2765 students were longitudinally followed up for two years. The prevalence of childhood overweight/obesity was increased between the 2019 and 2021 academic years (P < 0.001). During the COVID-19 pandemic, the rate of obesity remission significantly reduced by 7.9 % (P = 0.003), at a background of a plateau of obesity among children and adolescents. CONCLUSIONS: Our study provides evidence on the impact of school closure and home confinement as a standard infection control measure for the prevention of COVID-19, which are likely to break the balance between incidence of and remission from childhood obesity.


Subject(s)
COVID-19 , Pediatric Obesity , Adolescent , Humans , Child , Pediatric Obesity/epidemiology , COVID-19/epidemiology , COVID-19/prevention & control , Longitudinal Studies , Retrospective Studies , Hong Kong/epidemiology , Pandemics , Overweight/epidemiology
5.
Vaccine ; 40(7): 967-969, 2022 02 11.
Article in English | MEDLINE | ID: mdl-35063284

ABSTRACT

Vaccines against COVID-19 are now available for adolescents in Hong Kong but vaccine hesitancy is a major barrier to herd immunity. This survey study explores Hong Kong adolescents' attitudes towards the COVID-19 vaccination. 2609 adolescents from across Hong Kong completed an online survey focused on the intent to vaccinate and the reasons for their choice. 39% of adolescents intended to take the COVID-19 vaccination and significant factors for this decision include: having at least one parent vaccinated, knowing somebody diagnosed with COVID-19 and receiving the influenza vaccine. Adolescents' major concerns were either the safety and efficacy of the vaccine or the risk of infection. This study has proved that even in adolescents the vaccine hesitancy model is prominent with adolescents' intentions highly related to confidence in the vaccine and perception of disease risk. Future interventions should target these specific concerns to ensure adolescents are well educated to overcome vaccine hesitancy.


Subject(s)
COVID-19 , Influenza Vaccines , Adolescent , Attitude , COVID-19 Vaccines , Cross-Sectional Studies , Humans , SARS-CoV-2 , Vaccination
6.
ScientificWorldJournal ; 2012: 542983, 2012.
Article in English | MEDLINE | ID: mdl-22927783

ABSTRACT

OBJECTIVE: We examined the hypothesis that foetal exposure to maternal passive smoking is associated with childhood asthma, allergic rhinitis, and eczema. METHODS. The study was a population-based cross-sectional survey of Hong Kong Chinese children aged ≤14 years carried out in 2005 to 2006. RESULTS. Foetal exposure to maternal passive smoking was significantly associated with wheeze ever (OR 2.05; 95% CI 1.58-2.67), current wheeze (OR 2.06; 95% CI 1.48-2.86), allergic rhinitis ever (OR 1.22; 95% CI 1.09-1.37), and eczema ever (OR 1.61; 95% CI 1.38-1.87). Foetal exposure to maternal active smoking was significantly associated with asthma ever (OR 2.10; 95% CI 1.14-3.84), wheeze ever (OR 2.46; 95% CI 1.27-4.78), and current wheeze (OR 2.74; 95% CI 1.24-6.01) but not with allergic rhinitis ever (OR 1.01; 95% CI 0.70-1.46) or eczema ever (OR 1.38; 95% CI 0.87-2.18). The dose response relationship between wheeze ever and current wheeze with increasing exposure, from no exposure to maternal passive smoking and then to maternal active smoking, further supports causality. CONCLUSION. There is significant association between foetal exposure to maternal passive smoking and maternal active smoking with childhood asthma and related atopic illnesses. Further studies are warranted to explore the potential causal relationship.


Subject(s)
Asthma/etiology , Eczema/etiology , Prenatal Exposure Delayed Effects/etiology , Rhinitis, Allergic, Perennial/etiology , Tobacco Smoke Pollution/adverse effects , Asthma/epidemiology , Child , Child, Preschool , Confidence Intervals , Cross-Sectional Studies , Dose-Response Relationship, Drug , Eczema/epidemiology , Female , Hong Kong/epidemiology , Humans , Infant , Male , Odds Ratio , Pregnancy , Prenatal Exposure Delayed Effects/epidemiology , Prevalence , Rhinitis, Allergic , Rhinitis, Allergic, Perennial/epidemiology , Surveys and Questionnaires
7.
Lupus ; 21(1): 75-83, 2012 Jan.
Article in English | MEDLINE | ID: mdl-22004975

ABSTRACT

OBJECTIVE: Systemic lupus erythematosus (SLE) is a prototypic autoimmune disease with complex genetic inheritance. CD247 (CD3Z, TCRZ) plays a vital role in antigen recognition and signal transduction in antigen-specific immune responses, and is known to be involved in SLE pathogenesis. Weak disease association was reported for genetic variants in this gene in Caucasian studies for SLE, Crohn's disease and systemic sclerosis, but its role as a genetic risk factor was never firmly established. METHODS: In this study, using a collection of 612 SLE patients and 2193 controls of Chinese ethnicity living in Hong Kong in a genome-wide study, single nucleotide polymorphisms (SNPs) in and around CD247 were identified as being associated with SLE. The two most significant SNPs in this locus were selected for further replication using TaqMan genotyping assay in 3339 Asian patients from Hong Kong, Mainland China, and Thailand, as well as 4737 ethnically and geographically matched controls. RESULTS: The association of CD247 with SLE in Asian populations was confirmed (rs704853: odds ratio [OR] = 0. 81, p = 2.47 × 10(-7); rs858543: OR = 1.10, p = 0.0048). Patient-only analysis suggested that rs704853 is also linked to oral ulcers, hematologic disorders and anti-double-stranded DNA (dsDNA) antibody production. CONCLUSION: A significant association between variants in CD247 and SLE was demonstrated in Asian populations. Understanding the involvement of CD247 in SLE may shed new light on disease mechanisms and development of new treatment paradigms.


Subject(s)
Asian People/genetics , CD3 Complex/genetics , Lupus Erythematosus, Systemic/genetics , Lupus Erythematosus, Systemic/immunology , Adult , China , Genetic Predisposition to Disease , Genome-Wide Association Study , Genotype , Hong Kong , Humans , Linkage Disequilibrium , Odds Ratio , Polymorphism, Single Nucleotide , Thailand
8.
Genes Immun ; 12(3): 231-4, 2011 Apr.
Article in English | MEDLINE | ID: mdl-21326321

ABSTRACT

UHRF1BP1 encodes a highly conserved protein with unknown function. Previously, a coding variant in this gene was found to be associated with systemic lupus erythematosus (SLE) in populations of European ancestry (rs11755393, R454Q, P=2.22 x 10⁻8, odds ratio=1.17). In this study, by a combination of genome-wide study and replication involving a total of 1230 patients and 3144 controls, we confirmed the association of this coding variant to SLE in Hong Kong Chinese. We also identified another coding variant in this gene that independently contributes to SLE susceptibility (rs13205210, M1098T, P=4.44 x 10⁻9, odds ratio=1.49). Cross-population confirmation establishes the involvement of this locus in SLE and indicates that distinct alleles are contributing to disease susceptibility.


Subject(s)
Asian People/genetics , CCAAT-Enhancer-Binding Proteins/genetics , Lupus Erythematosus, Systemic/genetics , Mutation, Missense/genetics , Alleles , Amino Acid Sequence , Gene Frequency , Gene Order , Genetic Predisposition to Disease/genetics , Genome-Wide Association Study , Hong Kong , Humans , Linkage Disequilibrium , Polymorphism, Single Nucleotide/genetics , Ubiquitin-Protein Ligases
10.
Genes Immun ; 10(5): 414-20, 2009 Jul.
Article in English | MEDLINE | ID: mdl-19357697

ABSTRACT

Systemic lupus erythematosus (SLE) is a prototypic autoimmune disease with complex genetic inheritance. Recently, single nucleotide polymorphisms (SNPs) in BANK1 and TNFSF4 have been shown to be associated with SLE in Caucasian populations, but it is not known whether they are also involved in the disease in other ethnic groups. Recent data from our genome-wide association study (GWAS) for 314 SLE cases and 920 controls collected in Hong Kong identified SNPs in and around BANK1 and TNFSF4 to be associated with SLE risk. On the basis of the results of the reported studies and our GWAS, SNPs were selected for further genotyping in 949 SLE patients (overlapping with the 314 cases in our GWAS) and non-overlapping 1042 healthy controls. We confirmed the associations of BANK1 and TNFSF4 with SLE in Chinese (BANK1, rs3733197, odds ratio (OR)=0.84, P=0.021; BANK1, rs17266594, OR=0.61, P=4.67 x 10(-9); TNFSF4, rs844648, OR=1.22, P=2.47 x 10(-3); TNFSF4, rs2205960, OR=1.30, P=2.41 x 10(-4)). Another SNP located in intron 1 of BANK1, rs4522865, was separately replicated by Sequenom in 360 cases and 360 controls and was also confirmed to be associated with SLE (OR=0.725, P=2.93 x 10(-3)). Logistic regression analysis showed that rs3733197 (A383T in ankyrin domain) and rs17266594 (a branch point-site SNP) from BANK1 had independent contributions towards the disease association (P=0.037 and 6.63 x 10(-8), respectively). In TNFSF4, rs2205960 was associated with SLE independently from the effect of rs844648 (P=6.26 x 10(-3)), but not vice versa (P=0.55). These findings suggest that multiple independent genetic variants may be present within the gene locus, which exert their effects on SLE pathogenesis through different mechanisms.


Subject(s)
Adaptor Proteins, Signal Transducing/genetics , Asian People/genetics , Lupus Erythematosus, Systemic/ethnology , Lupus Erythematosus, Systemic/genetics , Membrane Proteins/genetics , OX40 Ligand/genetics , Epistasis, Genetic , Genome-Wide Association Study , Hong Kong/epidemiology , Humans , Polymorphism, Single Nucleotide , White People/genetics
11.
Genes Immun ; 10(3): 219-26, 2009 Apr.
Article in English | MEDLINE | ID: mdl-19225526

ABSTRACT

In this study, we compared the association of several newly discovered susceptibility genes for systemic lupus erythematosus (SLE) between populations of European origin and two Asian populations. Using 910 SLE patients and 1440 healthy controls from Chinese living in Hong Kong, and 278 SLE patients and 383 controls in Thailand, we studied association of STAT4, BLK and PXK with the disease. Our data confirmed association of STAT4 (rs7574865, odds ratio (OR) =1.71, P=3.55 x 10(-23)) and BLK (rs13277113, OR=0.77, P=1.34 x 10(-5)) with SLE. It was showed that rs7574865 of STAT4 is also linked to hematologic disorders and potentially some other subphenotypes of the disease. More than one genetic variant in STAT4 were found to be associated with the disease independently in our populations (rs7601754, OR=0.59, P=1.39 x 10(-9), and P=0.00034 when controlling the effect of rs7574865). With the same set of samples, however, our study did not detect any significant disease association for PXK, a risk factor for populations of European origin (rs6445975, joint P=0.36, OR=1.06, 95% confidence interval: 0.93-1.21). Our study indicates that some of the susceptibility genes for this disease may be population specific.


Subject(s)
Genetic Predisposition to Disease , Intracellular Signaling Peptides and Proteins/genetics , Lupus Erythematosus, Systemic/genetics , Nerve Tissue Proteins/genetics , Protein Serine-Threonine Kinases/genetics , STAT4 Transcription Factor/genetics , Adult , Female , Genotype , Hong Kong , Humans , Linkage Disequilibrium , Male , Middle Aged , Polymorphism, Single Nucleotide/genetics
13.
Rheumatology (Oxford) ; 46(8): 1290-6, 2007 Aug.
Article in English | MEDLINE | ID: mdl-17522097

ABSTRACT

OBJECTIVES: We postulate that patients with systemic lupus erythematosus (SLE) having recurrent infections are more likely to have poorer disease outcome. The aim of this study is to describe the pattern of infections and disease damage that occurred in a cohort of patients with juvenile-onset SLE, and to find out whether cumulative disease damage was associated with recurrent infections in these patients. METHOD: We retrospectively reviewed (1988-2004) the clinical characteristics, infective complications, and disease damage as measured by the Systemic Lupus International Collaborating Clinics/American College of Rheumatology (SLICC/ACR) Damage Index (SDI) in 47 juvenile-onset SLE patients. Potential risk factors for disease damage were evaluated by univariate analysis and logistic regression. The correlation between number of major infections and disease damage was determined. RESULTS: Thirty-two (68.1%) patients had lupus nephropathy and 16 patients (34%) had neuropsychiatric lupus. Sixty-one episodes of major infections, defined as infections requiring more than 1 week of antimicrobial agents, occurred in 27 patients (57.4%), and 18 patients (31.4%) had recurrent major infections (>/= 2 episodes). Organ damage (SDI >/= 1) was documented in 21 subjects (44.7%). By logistic regression, occurrence of major infections (P < 0.001) was the only significant risk factor for disease damage. There was a positive correlation between SDI score with the number of recurrent major infections (Spearman's correlation coefficient = 0.50, P < 0.001). CONCLUSION: Infections and disease damage are common co-morbidities in juvenile-onset SLE. Recurrent infections could predict poorer disease outcome and associated organ damage in SLE.


Subject(s)
Lupus Erythematosus, Systemic/complications , Opportunistic Infections/complications , Adolescent , Child , Child, Preschool , Female , Humans , Lupus Nephritis/complications , Lupus Vasculitis, Central Nervous System/complications , Male , Prognosis , Recurrence , Retrospective Studies , Risk Factors
14.
J Dent Res ; 86(5): 431-5, 2007 May.
Article in English | MEDLINE | ID: mdl-17452563

ABSTRACT

The prevalence of root-surface caries is increasing. We hypothesized that some restorative materials are protective against cariogenic challenge on root surfaces. Our goal was to study the effects of different restorative materials on root surfaces incubated with an oral biofilm generated in an artificial mouth. A biofilm of Streptococcus mutans, Streptococcus sobrinus, Lactobacillus rhamnosus, and Actinomyces naeslundii was co-cultured for 21 days on 24 glass-ionomer cement, resin-modified glass-ionomer cement, or resin-composite-restored root surfaces. These surfaces were then examined with Fourier transform infrared spectroscopy and scanning electron energy-dispersive spectroscopy. Only glass-ionomer restorations showed a significant increase in log calcium-to-phosphorus ratio (P < 0.01), and a significantly lower log amide I-to-hydrogen phosphate ratio on the root surface after incubation in the artificial mouth. Glass-ionomer restoratives conferred a preventive effect on the root surfaces against initial cariogenic challenge with a mixed-species oral biofilm without therapeutic intervention.


Subject(s)
Cariostatic Agents/therapeutic use , Dental Plaque/microbiology , Dental Plaque/prevention & control , Glass Ionomer Cements/therapeutic use , Root Caries/prevention & control , Actinomyces , Biofilms , Calcium/analysis , Composite Resins/therapeutic use , Dental Restoration, Permanent , Electron Probe Microanalysis , Humans , Lacticaseibacillus rhamnosus , Phosphorus/analysis , Resins, Synthetic/therapeutic use , Spectroscopy, Fourier Transform Infrared , Streptococcus mutans , Streptococcus sobrinus
15.
Ultrasound Obstet Gynecol ; 29(4): 395-400, 2007 Apr.
Article in English | MEDLINE | ID: mdl-17330321

ABSTRACT

OBJECTIVE: To determine fetal myocardial performance in pregnancies complicated by mild gestational impaired glucose tolerance (GIGT). METHODS: Ultrasound examinations were performed in 37 pregnant women with mild GIGT (36 did not require insulin) and in 44 controls at 18-24, 26-30 and 34-37 weeks of gestation. The thickness of the fetal ventricular walls and interventricular septum were measured by M-mode echocardiography. Using conventional Doppler echocardiography, the mitral and tricuspid early (E) and late (A) diastolic velocities and the ventricular myocardial performance index (MPI) were determined. RESULTS: The fetuses of women with GIGT had a greater abdominal circumference (P = 0.02), a larger amniotic fluid index (P = 0.03), and a tendency to be heavier (P = 0.058) at the third scan. There were no significant differences in myocardial thickness, mitral and tricuspid E and A velocities, and E/A ratios between study and control groups. The left and right ventricular MPIs, while similar between the two groups in the first and second scans, had decreased significantly by late gestation in the GIGT fetuses (P for trend = 0.018 and 0.014, respectively) and were significantly lower than those of the control group (P = 0.002 and 0.0008, respectively). CONCLUSIONS: Fetuses of women with mild GIGT lack the ventricular hypertrophy and diastolic dysfunction that is common in fetuses of diabetic mothers, and they have a decreased MPI late in gestation. Published by John Wiley & Sons, Ltd.


Subject(s)
Diabetes, Gestational , Fetal Heart/physiopathology , Glucose Intolerance , Adult , Blood Flow Velocity , Echocardiography, Doppler , Female , Fetal Development , Fetal Heart/diagnostic imaging , Gestational Age , Glucose Tolerance Test , Heart Rate, Fetal , Humans , Mitral Valve/diagnostic imaging , Pregnancy , Tricuspid Valve/diagnostic imaging , Ultrasonography, Prenatal
16.
Rheumatology (Oxford) ; 46(2): 220-6, 2007 Feb.
Article in English | MEDLINE | ID: mdl-16837471

ABSTRACT

OBJECTIVE: Cyclin-dependent kinase inhibitor 1A (p21) is a negative regulator in the cell cycle. Development of sex-linked lupus-like syndrome in p21-/- mice and reduced p21 gene expression in patients with systemic lupus erythematosus (SLE) compared with those in healthy controls suggested that p21 is a susceptibility gene of SLE. We investigated the same by a case-control association study. METHODS: Six single nucleotide polymorphisms, p21US G/A, p21DS C/A, p21-1022 G/A, p21C31 C/A, p21In2 G/C and p21UTR T/C, were genotyped in 516 SLE patients and 693 healthy controls. Association of genotypes and alleles with disease, disease phenotypes, haplotypes construction, linkage disequilibrium analysis and p21 mRNA expression were performed. RESULTS: We found a significant association of p21US A allele (OR = 0.23, 95% CI: 0.14-0.38, P < 0.001) and p21-1022 A allele (OR = 1.95, 95% CI: 1.37-2.78, P < 0.001) with SLE. We identified significant differences in the frequencies of haplotypes ht1-ACACCC, which contains p21US A allele, and ht2-GCACCC, which contains p21-1022 A allele, between SLE patients and controls (P < 0.0001). Besides, the p21US GA was associated with SLE patients suffering from arthritis (P = 0.003). We also observed differential p21 mRNA expressions among different genotypes of p21US and p21-1022 which were statistically significant. CONCLUSION: Our results suggested that the p21US A allele and p21-1022 A allele were both associated with the development of SLE, and the p21US A allele was associated with arthritis in SLE patients.


Subject(s)
Cyclin-Dependent Kinase Inhibitor p21/genetics , Lupus Erythematosus, Systemic/genetics , Polymorphism, Single Nucleotide , Adult , Case-Control Studies , Cyclin-Dependent Kinase Inhibitor p21/biosynthesis , Female , Gene Expression , Gene Frequency , Genetic Predisposition to Disease , Genotype , Haplotypes , Humans , Linkage Disequilibrium , Lupus Erythematosus, Systemic/blood , Male , Middle Aged , Phenotype , RNA, Messenger/genetics
17.
J Dent ; 35(5): 377-82, 2007 May.
Article in English | MEDLINE | ID: mdl-17174463

ABSTRACT

OBJECTIVES: There is increasing prevalence of root caries. We hypothesized different biofilms will cause varying demineralization in cementum. This study investigated the extent of demineralization of cementum by oral biofilm formed from three major cariogenic microorganisms: Streptococcus mutans, Lactobacillus acidophilus, and Actinomyces israelii. Sound cementum tooth blocks were incubated with mono-, bi-, and tri-species combinations of the bacteria under investigation. MATERIALS AND METHODS: The matrix (amide I) and phosphate content of the lesions was analyzed by Fourier-transform infrared spectroscopy (FTIR), and calcium and phosphorus levels were analyzed by scanning electron microscopy and energy-dispersive spectroscopy (SEM-EDX). RESULTS: The log[amide I:HPO(4)(2-) absorbance] values showed that A. israelii mono-culture caused significantly more demineralization than the other bacterial cultures. log[Ca:P] showed that all carious lesions were confined to the cementum. CONCLUSIONS: Oral biofilm arising from bacterial species A. israelii alone was the most cariogenic of those tested and produced the most demineralization in incipient carious lesions in cementum.


Subject(s)
Actinomyces/pathogenicity , Dental Cementum/microbiology , Lactobacillus acidophilus/pathogenicity , Root Caries/microbiology , Streptococcus mutans/pathogenicity , Analysis of Variance , Bicuspid , Biofilms , Coculture Techniques , Dental Cementum/pathology , Electron Probe Microanalysis , Humans , Spectroscopy, Fourier Transform Infrared , Tooth Demineralization/microbiology
18.
Clin Exp Allergy ; 36(9): 1138-46, 2006 Sep.
Article in English | MEDLINE | ID: mdl-16961713

ABSTRACT

OBJECTIVE: To examine the association of air pollutants with hospital admission for childhood asthma in Hong Kong. METHODS: Data on hospital admissions for asthma, influenza and total hospital admissions in children aged < or =18 years at all Hospital Authority hospitals during 1997-2002 were obtained. Data on daily mean concentrations of particles with aerodynamic diameter <10 microm (i. e. PM10) and <2.5 microm (i. e. PM2.5), nitrogen dioxide (NO2), sulphur dioxide (SO2), and ozone (O3) and data on meteorological variables were associated with asthma hospital admissions using Poisson's regression with generalized additive models for correction of yearly trend, temperature, humidity, day-of-week effect, holiday, influenza admissions and total hospital admission. The possibility of a lag effect of each pollutant and the interaction of different pollutants were also examined. RESULTS: The association between asthma admission with change of NO2, PM10, PM2.5 and O3 levels remained significant after adjustment for multi-pollutants effect and confounding variables, with increase in asthma admission rate of 5.64% (3.21-8.14) at lag 3 for NO2, 3.67% (1.52-5.86) at lag 4 for PM10, 3.24% (0.93-5.60) at lag 4 for PM2.5 and 2.63% (0.64-4.67) at lag 2 for O3. Effect of SO2 was lost after adjustment. CONCLUSION: Ambient levels of PM10, PM2.5) NO2 and O3 are associated with childhood asthma hospital admission in Hong Kong.


Subject(s)
Air Pollutants/toxicity , Asthma/chemically induced , Adolescent , Asthma/epidemiology , Child , Environmental Exposure/adverse effects , Hong Kong/epidemiology , Hospitalization , Humans , Humidity , Nitrogen Dioxide/toxicity , Oxidants, Photochemical/toxicity , Ozone/toxicity , Particle Size , Rain , Seasons , Sulfur Dioxide/toxicity , Temperature
19.
AJNR Am J Neuroradiol ; 27(1): 51-4, 2006 Jan.
Article in English | MEDLINE | ID: mdl-16418355

ABSTRACT

BACKGROUND AND PURPOSE: By using a neonatal rat hypoxia-ischemia (HI) model, we studied the relationship between lesion volume-measured by diffusion-weighted imaging (DWI) and T2-weighted imaging (T2WI) at an early time point-and irreversible infarct volume. We also evaluated the optimal apparent diffusion coefficient (ADC) threshold that provides the best correlation with irreversible infarct size. MATERIALS AND METHODS: Twenty-three neonatal rats underwent right common carotid artery ligation and hypoxia. MR imaging was performed 1-2 hours post-HI by using DWI and T2WI and at day 4 post-HI by using T2WI. Lesion volumes relative to whole brain (%LV) were measured on ADC maps by using different relative ADC thresholds 60%-80% of mean contralateral ADC and T2WI. Pearson correlation and multiple linear regression analysis were used to study the relationships between ln(%LV) at MR imaging and %LV at histopathology. RESULTS: At 1-2 hours post-HI, all lesion volume measurements on DWI were significantly correlated with the infarct volume on histopathology, with the best correlation attained at the 80% ADC threshold (r = 0.738; P < .001). The estimated regression formula was %LV on histopathology = 20.60 + 3.33 ln(%LV on 80% ADC threshold) (adjusted R(2) = 0.523; P < .001). Lesion volume at 1-2 hours post-HI tended to underestimate the final infarct volume. CONCLUSION: Early post-HI MR imaging by using DWI correlates moderately well with the size of irreversible infarct, especially when measured by using a relative ADC threshold of 80% mean contralateral ADC.


Subject(s)
Brain/pathology , Cerebral Infarction/diagnosis , Hypoxia-Ischemia, Brain/diagnosis , Magnetic Resonance Imaging , Animals , Animals, Newborn , Cerebral Infarction/etiology , Cerebral Infarction/pathology , Diffusion Magnetic Resonance Imaging , Hypoxia-Ischemia, Brain/complications , Hypoxia-Ischemia, Brain/pathology , Rats , Rats, Sprague-Dawley
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