Paediatrics (RCH) - Research Publications

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    Neonatal DNA methylation profile in human twins is specified by a complex interplay between intrauterine environmental and genetic factors, subject to tissue-specific influence
    Gordon, L ; Joo, JE ; Powel, JE ; Ollikainen, M ; Novakovic, B ; Li, X ; Andronikos, R ; Cruickshank, MN ; Conneely, KN ; Smith, AK ; Alisch, RS ; Morley, R ; Visscher, PM ; Craig, JM ; Saffery, R (COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT, 2012-08)
    Comparison between groups of monozygotic (MZ) and dizygotic (DZ) twins enables an estimation of the relative contribution of genetic and shared and nonshared environmental factors to phenotypic variability. Using DNA methylation profiling of ∼20,000 CpG sites as a phenotype, we have examined discordance levels in three neonatal tissues from 22 MZ and 12 DZ twin pairs. MZ twins exhibit a wide range of within-pair differences at birth, but show discordance levels generally lower than DZ pairs. Within-pair methylation discordance was lowest in CpG islands in all twins and increased as a function of distance from islands. Variance component decomposition analysis of DNA methylation in MZ and DZ pairs revealed a low mean heritability across all tissues, although a wide range of heritabilities was detected for specific genomic CpG sites. The largest component of variation was attributed to the combined effects of nonshared intrauterine environment and stochastic factors. Regression analysis of methylation on birth weight revealed a general association between methylation of genes involved in metabolism and biosynthesis, providing further support for epigenetic change in the previously described link between low birth weight and increasing risk for cardiovascular, metabolic, and other complex diseases. Finally, comparison of our data with that of several older twins revealed little evidence for genome-wide epigenetic drift with increasing age. This is the first study to analyze DNA methylation on a genome scale in twins at birth, further highlighting the importance of the intrauterine environment on shaping the neonatal epigenome.
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    The threat among us: significance and scale of diabetic chronic kidney disease in Australia
    Lecamwasam, A ; Ekinci, EI ; MacIsaac, RJ ; Saffery, R ; Dwyer, KM (WILEY, 2017-12)
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    Genetic variation at the Th2 immune gene IL13 is associated with IgE-mediated paediatric food allergy
    Ashley, SE ; Tan, H-TT ; Peters, R ; Allen, KJ ; Vuillermin, P ; Dharmage, SC ; Tang, MLK ; Koplin, J ; Lowe, A ; Ponsonby, A-L ; Molloy, J ; Matheson, MC ; Saffery, R ; Ellis, JA ; Martino, D (WILEY, 2017-08)
    BACKGROUND: Food allergies pose a considerable world-wide public health burden with incidence as high as one in ten in 12-month-old infants. Few food allergy genetic risk variants have yet been identified. The Th2 immune gene IL13 is a highly plausible genetic candidate as it is central to the initiation of IgE class switching in B cells. OBJECTIVE: Here, we sought to investigate whether genetic polymorphisms at IL13 are associated with the development of challenge-proven IgE-mediated food allergy. METHOD: We genotyped nine IL13 "tag" single nucleotide polymorphisms (tag SNPs) in 367 challenge-proven food allergic cases, 199 food-sensitized tolerant cases and 156 non-food allergic controls from the HealthNuts study. 12-month-old infants were phenotyped using open oral food challenges. SNPs were tested using Cochran-Mantel-Haenszel test adjusted for ancestry strata. A replication study was conducted in an independent, co-located sample of four paediatric cohorts consisting of 203 food allergic cases and 330 non-food allergic controls. Replication sample phenotypes were defined by clinical history of reactivity, 95% PPV or challenge, and IL13 genotyping was performed. RESULTS: IL13 rs1295686 was associated with challenge-proven food allergy in the discovery sample (P=.003; OR=1.75; CI=1.20-2.53). This association was also detected in the replication sample (P=.03, OR=1.37, CI=1.03-1.82) and further supported by a meta-analysis (P=.0006, OR=1.50). However, we cannot rule out an association with food sensitization. Carriage of the rs1295686 variant A allele was also associated with elevated total plasma IgE. CONCLUSIONS AND CLINICAL RELAVANCE: We show for the first time, in two independent cohorts, that IL13 polymorphism rs1295686 (in complete linkage disequilibrium with functional variant rs20541) is associated with challenge-proven food allergy.
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    The skin barrier function gene SPINK5 is associated with challenge-proven IgE-mediated food allergy in infants
    Ashley, SE ; Tan, H-TT ; Vuillermin, P ; Dharmage, SC ; Tang, MLK ; Koplin, J ; Gurrin, LC ; Lowe, A ; Lodge, C ; Ponsonby, A-L ; Molloy, J ; Martin, P ; Matheson, MC ; Saffery, R ; Allen, KJ ; Ellis, JA ; Martino, D (WILEY, 2017-09)
    BACKGROUND: A defective skin barrier is hypothesized to be an important route of sensitization to dietary antigens and may lead to food allergy in some children. Missense mutations in the serine peptidase inhibitor Kazal type 5 (SPINK5) skin barrier gene have previously been associated with allergic conditions. OBJECTIVE: To determine whether genetic variants in and around SPINK5 are associated with IgE-mediated food allergy. METHOD: We genotyped 71 "tag" single nucleotide polymorphisms (tag-SNPs) within a region spanning ~263 kb including SPINK5 (~61 kb) in n=722 (n=367 food-allergic, n=199 food-sensitized-tolerant and n=156 non-food-allergic controls) 12-month-old infants (discovery sample) phenotyped for food allergy with the gold standard oral food challenge. Transepidermal water loss (TEWL) measures were collected at 12 months from a subset (n=150) of these individuals. SNPs were tested for association with food allergy using the Cochran-Mantel-Haenszel test adjusting for ancestry strata. Association analyses were replicated in an independent sample group derived from four paediatric cohorts, total n=533 (n=203 food-allergic, n=330 non-food-allergic), mean age 2.5 years, with food allergy defined by either clinical history of reactivity, 95% positive predictive value (PPV) or challenge, corrected for ancestry by principal components. RESULTS: SPINK5 variant rs9325071 (A⟶G) was associated with challenge-proven food allergy in the discovery sample (P=.001, OR=2.95, CI=1.49-5.83). This association was further supported by replication (P=.007, OR=1.58, CI=1.13-2.20) and by meta-analysis (P=.0004, OR=1.65). Variant rs9325071 is associated with decreased SPINK5 gene expression in the skin in publicly available genotype-tissue expression data, and we generated preliminary evidence for association of this SNP with elevated TEWL also. CONCLUSIONS: We report, for the first time, association between SPINK5 variant rs9325071 and challenge-proven IgE-mediated food allergy.
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    Vitamin D insufficiency in the first 6 months of infancy and challenge-proven IgE-mediated food allergy at 1 year of age: a case-cohort study
    Molloy, J ; Koplin, JJ ; Allen, KJ ; Tang, MLK ; Collier, F ; Carlin, JB ; Saffery, R ; Burgner, D ; Ranganathan, S ; Dwyer, T ; Ward, AC ; Moreno-Betancur, M ; Clarke, M ; Ponsonby, AL ; Vuillermin, P (WILEY, 2017-08)
    BACKGROUND: Ecological evidence suggests vitamin D insufficiency (VDI) due to lower ambient ultraviolet radiation (UVR) exposure may be a risk factor for IgE-mediated food allergy. However, there are no studies relating directly measured VDI during early infancy to subsequent challenge-proven food allergy. OBJECTIVE: To prospectively investigate the association between VDI during infancy and challenge-proven food allergy at 1 year. METHODS: In a birth cohort (n = 1074), we used a case-cohort design to compare 25-hydroxyvitamin D3 (25(OH)D3 ) levels among infants with food allergy vs a random subcohort (n = 274). The primary exposures were VDI (25(OH)D3 <50 nM) at birth and 6 months of age. Ambient UVR and time in the sun were combined to estimate UVR exposure dose. IgE-mediated food allergy status at 1 year was determined by formal challenge. Binomial regression was used to examine associations between VDI, UVR exposure dose and food allergy and investigate potential confounding. RESULTS: Within the random subcohort, VDI was present in 45% (105/233) of newborns and 24% (55/227) of infants at 6 months. Food allergy prevalence at 1 year was 7.7% (61/786), and 6.5% (53/808) were egg-allergic. There was no evidence of an association between VDI at either birth (aRR 1.25, 95% CI 0.70-2.22) or 6 months (aRR 0.93, 95% CI 0.41-2.14) and food allergy at 1 year. CONCLUSIONS: There was no evidence that VDI during the first 6 months of infancy is a risk factor for food allergy at 1 year of age. These findings primarily relate to egg allergy, and larger studies are required.
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    The association between higher maternal pre-pregnancy body mass index and increased birth weight, adiposity and inflammation in the newborn
    McCloskey, K ; Ponsonby, A-L ; Collier, F ; Allen, K ; Tang, MLK ; Carlin, JB ; Saffery, R ; Skilton, MR ; Cheung, M ; Ranganathan, S ; Dwyer, T ; Burgner, D ; Vuillermin, P (WILEY, 2018-01)
    BACKGROUND: Excess adiposity and adiposity-related inflammation are known risk factors for cardiovascular disease in adults; however, little is known regarding the determinants of adiposity-related inflammation at birth. OBJECTIVES: The aim of this study was to investigate the association between maternal pre-pregnancy BMI and newborn adiposity and inflammation. METHODS: Paired maternal (28-week gestation) and infant (umbilical cord) blood samples were collected from a population-derived birth cohort (Barwon Infant Study, n = 1074). Data on maternal comorbidities and infant birth anthropomorphic measures were compiled, and infant aortic intima-media thickness was measured by trans-abdominal ultrasound. In a selected subgroup of term infants (n = 161), matched maternal and cord lipids, high-sensitivity C-reactive protein (hsCRP) and maternal soluble CD14 were measured. Analysis was completed by using pairwise correlation and linear regression. Because of their non-normal distribution, pathology blood measures were log transformed prior to analysis. RESULTS: Maternal pre-pregnancy BMI was positively associated with increased birth weight (mean difference 17.8 g per kg m-2 , 95% CI 6.6 to 28.9; p = 0.002), newborn mean skin-fold thickness (mean difference 0.1 mm per kg m-2 , 95% CI 0.0 to 0.1; p < 0.001) and cord blood hsCRP (mean difference of 4.2% increase in hsCRP per kg m-2 increase in pre-pregnancy BMI, 95% CI 0.6 to 7.7%, p = 0.02), but not cord blood soluble CD14. Inclusion of maternal hsCRP as a covariate attenuated the associations between pre-pregnancy BMI and both newborn skin-fold thickness and cord blood hsCRP. CONCLUSION: Higher maternal pre-pregnancy BMI is associated with increased newborn adiposity and inflammation. These associations may be partially mediated by maternal inflammation during pregnancy.
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    The CODATwins Project: The Current Status and Recent Findings of COllaborative Project of Development of Anthropometrical Measures in Twins
    Silventoinen, K ; Jelenkovic, A ; Yokoyama, Y ; Sund, R ; Sugawara, M ; Tanaka, M ; Matsumoto, S ; Bogl, LH ; Freitas, DL ; Maia, JA ; Hjelmborg, JVB ; Aaltonen, S ; Piirtola, M ; Latvala, A ; Calais-Ferreira, L ; Oliveira, VC ; Ferreira, PH ; Ji, F ; Ning, F ; Pang, Z ; Ordonana, JR ; Sanchez-Romera, JF ; Colodro-Conde, L ; Burt, SA ; Klump, KL ; Martin, NG ; Medland, SE ; Montgomery, GW ; Kandler, C ; McAdams, TA ; Eley, TC ; Gregory, AM ; Saudino, KJ ; Dubois, L ; Boivin, M ; Brendgen, M ; Dionne, G ; Vitaro, F ; Tarnoki, AD ; Tarnoki, DL ; Haworth, CMA ; Plomin, R ; Oncel, SY ; Aliev, F ; Medda, E ; Nistico, L ; Toccaceli, V ; Craig, JM ; Saffery, R ; Siribaddana, SH ; Hotopf, M ; Sumathipala, A ; Rijsdijk, F ; Jeong, H-U ; Spector, T ; Mangino, M ; Lachance, G ; Gatz, M ; Butler, DA ; Gao, W ; Yu, C ; Li, L ; Bayasgalan, G ; Narandalai, D ; Harden, KP ; Tucker-Drob, EM ; Christensen, K ; Skytthe, A ; Kyvik, KO ; Derom, CA ; Vlietinck, RF ; Loos, RJF ; Cozen, W ; Hwang, AE ; Mack, TM ; He, M ; Ding, X ; Silberg, JL ; Maes, HH ; Cutler, TL ; Hopper, JL ; Magnusson, PKE ; Pedersen, NL ; Dahl Aslan, AK ; Baker, LA ; Tuvblad, C ; Bjerregaard-Andersen, M ; Beck-Nielsen, H ; Sodemann, M ; Ullemar, V ; Almqvist, C ; Tan, Q ; Zhang, D ; Swan, GE ; Krasnow, R ; Jang, KL ; Knafo-Noam, A ; Mankuta, D ; Abramson, L ; Lichtenstein, P ; Krueger, RF ; McGue, M ; Pahlen, S ; Tynelius, P ; Rasmussen, F ; Duncan, GE ; Buchwald, D ; Corley, RP ; Huibregtse, BM ; Nelson, TL ; Whitfield, KE ; Franz, CE ; Kremen, WS ; Lyons, MJ ; Ooki, S ; Brandt, I ; Nilsen, TS ; Harris, JR ; Sung, J ; Park, HA ; Lee, J ; Lee, SJ ; Willemsen, G ; Bartels, M ; Van Beijsterveldt, CEM ; Llewellyn, CH ; Fisher, A ; Rebato, E ; Busjahn, A ; Tomizawa, R ; Inui, F ; Watanabe, M ; Honda, C ; Sakai, N ; Hur, Y-M ; Sorensen, TIA ; Boomsma, DI ; Kaprio, J (CAMBRIDGE UNIV PRESS, 2019-12)
    The COllaborative project of Development of Anthropometrical measures in Twins (CODATwins) project is a large international collaborative effort to analyze individual-level phenotype data from twins in multiple cohorts from different environments. The main objective is to study factors that modify genetic and environmental variation of height, body mass index (BMI, kg/m2) and size at birth, and additionally to address other research questions such as long-term consequences of birth size. The project started in 2013 and is open to all twin projects in the world having height and weight measures on twins with information on zygosity. Thus far, 54 twin projects from 24 countries have provided individual-level data. The CODATwins database includes 489,981 twin individuals (228,635 complete twin pairs). Since many twin cohorts have collected longitudinal data, there is a total of 1,049,785 height and weight observations. For many cohorts, we also have information on birth weight and length, own smoking behavior and own or parental education. We found that the heritability estimates of height and BMI systematically changed from infancy to old age. Remarkably, only minor differences in the heritability estimates were found across cultural-geographic regions, measurement time and birth cohort for height and BMI. In addition to genetic epidemiological studies, we looked at associations of height and BMI with education, birth weight and smoking status. Within-family analyses examined differences within same-sex and opposite-sex dizygotic twins in birth size and later development. The CODATwins project demonstrates the feasibility and value of international collaboration to address gene-by-exposure interactions that require large sample sizes and address the effects of different exposures across time, geographical regions and socioeconomic status.
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    Twin's Birth-Order Differences in Height and Body Mass Index From Birth to Old Age: A Pooled Study of 26 Twin Cohorts Participating in the CODATwins Project
    Yokoyama, Y ; Jelenkovic, A ; Sund, R ; Sung, J ; Hopper, JL ; Ooki, S ; Heikkila, K ; Aaltonen, S ; Tarnoki, AD ; Tarnoki, DL ; Willemsen, G ; Bartels, M ; van Beijsterveldt, TCEM ; Saudino, KJ ; Cutler, TL ; Nelson, TL ; Whitfield, KE ; Wardle, J ; Llewellyn, CH ; Fisher, A ; He, M ; Ding, X ; Bjerregaard-Andersen, M ; Beck-Nielsen, H ; Sodemann, M ; Song, Y-M ; Yang, S ; Lee, K ; Jeong, H-U ; Knafo-Noam, A ; Mankuta, D ; Abramson, L ; Burt, SA ; Klump, KL ; Ordonana, JR ; Sanhez-Romera, JF ; Colodro-Conde, L ; Harris, JR ; Brandt, I ; Nilsen, TS ; Craig, JM ; Saffery, R ; Ji, F ; Ning, F ; Pang, Z ; Dubois, L ; Boivin, M ; Brendgen, M ; Dionne, G ; Vitaro, F ; Martin, NG ; Medland, SE ; Montgomery, GW ; Magnusson, PKE ; Pedersen, NL ; Aslan, AKD ; Tynelius, P ; Haworth, CMA ; Plomin, R ; Rebato, E ; Rose, RJ ; Goldberg, JH ; Rasmussen, F ; Hur, Y-M ; Sorensen, TIA ; Boomsma, DI ; Kaprio, J ; Silventoinen, K (CAMBRIDGE UNIV PRESS, 2016-04)
    We analyzed birth order differences in means and variances of height and body mass index (BMI) in monozygotic (MZ) and dizygotic (DZ) twins from infancy to old age. The data were derived from the international CODATwins database. The total number of height and BMI measures from 0.5 to 79.5 years of age was 397,466. As expected, first-born twins had greater birth weight than second-born twins. With respect to height, first-born twins were slightly taller than second-born twins in childhood. After adjusting the results for birth weight, the birth order differences decreased and were no longer statistically significant. First-born twins had greater BMI than the second-born twins over childhood and adolescence. After adjusting the results for birth weight, birth order was still associated with BMI until 12 years of age. No interaction effect between birth order and zygosity was found. Only limited evidence was found that birth order influenced variances of height or BMI. The results were similar among boys and girls and also in MZ and DZ twins. Overall, the differences in height and BMI between first- and second-born twins were modest even in early childhood, while adjustment for birth weight reduced the birth order differences but did not remove them for BMI.
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    Associations between birth size and later height from infancy through adulthood: An individual based pooled analysis of 28 twin cohorts participating in the CODATwins project
    Jelenkovic, A ; Yokoyama, Y ; Sund, R ; Hur, Y-M ; Harris, JR ; Brandt, I ; Nilsen, TS ; Ooki, S ; Ullemar, V ; Almqvist, C ; Magnusson, PKE ; Saudino, KJ ; Stazi, MA ; Fagnani, C ; Brescianini, S ; Nelson, TL ; Whitfield, KE ; Knafo-Noam, A ; Mankuta, D ; Abramson, L ; Cutler, TL ; Hopper, JL ; Llewellyn, CH ; Fisher, A ; Corley, RP ; Huibregtse, BM ; Derom, CA ; Vlietinck, RF ; Bjerregaard-Andersen, M ; -Nielsen, HB ; Sodemann, M ; Krueger, RF ; McGue, M ; Pahlen, S ; Burt, SA ; Klump, KL ; Dubois, L ; Boivin, M ; Brendgen, M ; Dionne, G ; Vitaro, F ; Willemsen, G ; Bartels, M ; van Beijsterveld, CEM ; Craig, JM ; Saffery, R ; Rasmussen, F ; Tynelius, P ; Heikkila, K ; Pietilainen, KH ; Bayasgalan, G ; Narandalai, D ; Haworth, CMA ; Plomin, R ; Ji, F ; Ning, F ; Pang, Z ; Rebato, E ; Tarnoki, AD ; Tarnoki, DL ; Kim, J ; Lee, J ; Lee, S ; Sung, J ; Loos, RJF ; Boomsma, DI ; Sorensen, TIA ; Kaprio, J ; Silventoinen, K (ELSEVIER IRELAND LTD, 2018-05)
    BACKGROUND: There is evidence that birth size is positively associated with height in later life, but it remains unclear whether this is explained by genetic factors or the intrauterine environment. AIM: To analyze the associations of birth weight, length and ponderal index with height from infancy through adulthood within mono- and dizygotic twin pairs, which provides insights into the role of genetic and environmental individual-specific factors. METHODS: This study is based on the data from 28 twin cohorts in 17 countries. The pooled data included 41,852 complete twin pairs (55% monozygotic and 45% same-sex dizygotic) with information on birth weight and a total of 112,409 paired height measurements at ages ranging from 1 to 69 years. Birth length was available for 19,881 complete twin pairs, with a total of 72,692 paired height measurements. The association between birth size and later height was analyzed at both the individual and within-pair level by linear regression analyses. RESULTS: Within twin pairs, regression coefficients showed that a 1-kg increase in birth weight and a 1-cm increase in birth length were associated with 1.14-4.25 cm and 0.18-0.90 cm taller height, respectively. The magnitude of the associations was generally greater within dizygotic than within monozygotic twin pairs, and this difference between zygosities was more pronounced for birth length. CONCLUSION: Both genetic and individual-specific environmental factors play a role in the association between birth size and later height from infancy to adulthood, with a larger role for genetics in the association with birth length than with birth weight.
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    Telomere length and lung function in a population-based cohort of children and mid-life adults
    Minh, TN ; Saffery, R ; Burgner, D ; Lycett, K ; Vryer, R ; Grobler, A ; Dwyer, T ; Ranganathan, S ; Wake, M (WILEY, 2019-12)
    OBJECTIVE: Telomere length is associated with poorer lung health in older adults, possibly from cumulative risk factor exposure, but data are lacking in pediatric and population-based cohorts. We examined associations of telomere length with lung function in children and mid-life adults. METHODS: Data were drawn from a population-based cross-sectional study of 11 to 12 year-olds and mid-life adults. Lung function was assessed by spirometric FEV1 , FVC, FEV 1 /FVC ratio, and MMEF 25-75 . Telomere length was measured by quantitative polymerase chain reaction from blood and expressed as the amount of telomeric genomic DNA to the beta-globin gene (T/S ratio). Associations of telomere length with spirometric parameters were tested by linear and logistic regression models, adjusting for potential confounders of sex, age, body mass index, socioeconomic position, physical activity, inflammation, asthma, pubertal status, and smoking. RESULTS: Mean T/S ratio was 1.09 (n = 1206; SD 0.55) in children and 0.81 (n = 1343; SD 0.38) in adults. In adults, for every additional unit in T/S ratio, FEV 1 /FVC and MMEF 25-75 z-scores were higher (β 0.21 [95% confidence interval, CI; 0.06-0.36] and 0.23 [95% CI; 0.08-0.38], respectively), and the likelihood of being in the lowest quartile for FEV 1 /FVC and MMEF 25-75 z-scores was lower (odds ratios 0.59 [95% CI, 0.39-0.89] and 0.64 [95% CI, 0.41-0.99], respectively). No evidence of association was seen for adult FEV 1 or FVC, or any childhood spirometric index after adjustments. CONCLUSION: Shorter telomere length showed moderate associations with poorer airflow parameters, but not vital capacity (lung volume) in mid-life adults. However, there was no convincing evidence of associations in children.