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Birth size and gestational age in opposite-sex twins as compared to same-sex twins: An individual-based pooled analysis of 21 cohorts

Scientific Reportsvolume 8, Article number: 6300 (2018) | Download Citation


It is well established that boys are born heavier and longer than girls, but it remains unclear whether birth size in twins is affected by the sex of their co-twin. We conducted an individual-based pooled analysis of 21 twin cohorts in 15 countries derived from the COllaborative project of Development of Anthropometrical measures in Twins (CODATwins), including 67,850 dizygotic twin individuals. Linear regression analyses showed that boys having a co-twin sister were, on average, 31 g (95% CI 18 to 45) heavier and 0.16 cm (95% CI 0.045 to 0.274) longer than those with a co-twin brother. In girls, birth size was not associated (5 g birth weight; 95% CI −8 to −18 and −0.089 cm birth length; 95% CI −0.202 to 0.025) with the sex of the co-twin. Gestational age was slightly shorter in boy-boy pairs than in boy-girl and girl-girl pairs. When birth size was standardized by gestational age, the magnitude of the associations was attenuated in boys, particularly for birth weight. In conclusion, boys with a co-twin sister are heavier and longer at birth than those with a co-twin brother. However, these differences are modest and partly explained by a longer gestation in the presence of a co-twin sister.


Birth weight is an indicator of foetal growth and predicts short-term survival of the newborn1. It is also an indicator of processes that influence long-term health; for example, birth weight has been inversely associated with adult mortality, especially cardiovascular mortality, and positively associated with the risk of cancer deaths2. It is well established that boys are born heavier than girls, in both singletons3,4 and twins5,6,7. However, there is an ongoing debate as to whether birth weight in twins is affected not only by their own sex but also by the sex of their co-twin. Dizygotic twinning rate has shown a steep increase since the 1980s in most industrialized countries, mainly due to the widespread use of in vitro fertilization and other fertility treatments8,9. Therefore, the study of the association between birth weight and the sex of the co-twin is of clinical and epidemiological interest.

Some studies have shown that boys from opposite-sex (OS) pairs are significantly heavier at birth than boys from same-sex (SS) pairs10,11,12, but this difference did not reach significance in other studies13,14,15,16. The greater birth weight of boys from OS pairs has generally been ascribed to a more successful in utero competition for nutrients of boys in the presence of a sister rather than a brother co-twin17. For girls, findings are less consistent. Girls from OS pairs were heavier at birth than those from SS pairs in Canadian twins18; similar but non-significant differences were observed in other populations13,15,19. Since androgens have shown to exert a positive effect on fetal growth20, a so-called twin testosterone transfer (TTT) hypothesis has been proposed15, by which females who develop with a male co-twin are potentially exposed to higher levels of prenatal testosterone (the most potent androgen) than females who develop with a female co-twin. This would then explain the greater birth weight in girls from OS than from SS pairs. However, other studies have reported roughly similar mean birth weight in girls from SS and OS pairs11,12 and, although non-significant, greater birth weight in SS twins14. Part of the discrepancy between findings might be explained by the different criteria used to select SS twins in the studies (all SS twins (monozygotic and dizygotic), SS dichorionic twins or only SS dizygotic twins).

According to studies in singletons showing that mean duration of gestation is shorter in boys than in girls21,22, there is evidence that boy-boy pairs have a shorter gestation than boy-girl pairs and girl-girl pairs; however, it is not clear whether gestational age differs between boy-girl pairs and girl-girl pairs11,12,16. Loos et al.12 observed that when controlling for the length of gestation, the birth weight differences between boys from SS and boys from OS pairs attenuated, suggesting that gestational age has an important role and that boys from OS pairs benefited from the slightly longer gestation. This study12 additionally showed that gestational age difference between boys and girls is smaller with greater birth weight, which confirmed the findings in singletons22.

Although birth weight is the most widely used measure of birth size in epidemiological studies23, alternative measures, such as birth length and ponderal index (PI), have also been of interest. PI is a measure of relative weight (assessed as birth weight per birth length cubed) that is more appropriate for newborns than body mass index. For example, short birth length has been found to be associated with adult all-cause mortality24,25 and greater PI with a higher risk of breast cancer mortality26. Birth length is also greater in boys than in girls6, but only one study compared SS and OS twins showing no differences18. Using only dizygotic (SS and OS) twins from 21 cohorts in 15 countries, we conducted an individual-based analysis of pooled twin cohorts (i) to analyze the association of co-twin’s sex with birth weight, length and PI, (ii) to ascertain whether gestational age differs between the three twin pair types (boy-boy, boy-girl and girl-girl) and (iii) to examine whether gestational age plays a role in the association between co-twin’s sex and the three indicators of birth size.

Material and Methods


All participants were volunteers and they or their parents gave informed consent when participating in their original studies. No experimental data were asked and thus we did not ask ethical approval. Only a limited set of observational variables and anonymized data were delivered to the data management center at University of Helsinki. The pooled analysis was approved by the ethical committee of Department of Public Health, University of Helsinki, and the methods were carried out in accordance with the approved guidelines.


This study is based on the data from the COllaborative project of Development of Anthropometrical measures in Twins (CODATwins), which was intended to pool data from all twin projects in the world having information on height and weight27. Information on birth weight of both SS and OS dizygotic twins was available for 21 twin cohorts from 15 countries (OS/SS ratio range = 0.3–2.2). Birth length and gestational age were available in 12 and 13 of these cohorts, respectively. The participating twin cohorts are identified in Table 1 (footnote) and were previously described in detail27.

Table 1 Descriptive statistics and regression coefficients for the difference in birth size of dizygotic twin boys and girls according to the sex of their co-twin (reference group same-sex dizygotic twins).

After excluding monozygotic twins (n = 39,590), we had 70,814 dizygotic twin individuals with information on birth weight (Fig. 1). We removed individuals with birth weight <0.5 or >5 kg, or born before 1940 because there were too few of them for meaningful analyses. We next excluded individuals without data on their co-twins or with intra-pair difference in birth weight >1.5 kg leaving 67,850 individuals (33,925 complete twin pairs; 52% SS and 48% OS). For the analyses on birth length and PI [weight (kg)/height (m3)], we additionally excluded individuals without data on birth length, with birth length <25 or >60 cm, PI <12 or >38 kg/m3, intrapair difference in birth length >10 cm or PI >12 kg/m3, or born before 1970 leaving 33,170 individuals (16,585 complete twin pairs; 51% SS and 49% OS). These cut-off limits were defined based on the visual inspection of histograms for both birth size measures and intrapair differences in birth size.

Figure 1
Figure 1

Flow chart of sample selection in the study. CODATwins: COllaborative project of Development of Anthropometrical measures in Twins; individuals: twin individuals; pairs: twin pairs.

For the analyses involving gestational age, from the 67,850 individuals with information on birth weight, we excluded twin individuals without data on gestational age and gestational age <25 or >45 weeks resulting in 23,923 twin pairs. Gestational age was defined as a categorical variable indicating completed weeks of gestation. We visually inspected histograms for each gestational week and removed unrealistic values for birth weight, length and PI for a given gestation (<0.2% for birth weight and <0.4% for birth length and PI). We further calculated birth weight, length and PI standardized by gestational age. These three measures of size at birth were expressed as SD scores of the respective means/weeks of gestation (z-scores; i.e., mean = 0 and SD = 1) to estimate their relative value for a given gestational age. Finally, birth weight standardized by gestational age was available for 23,870 twin pairs and birth length and PI standardized by gestational age for 14,890 twin pairs.

Statistical analyses

Statistical analyses were conducted using the Stata statistical software package (version 12.0; StataCorp, College Station, Texas, USA). To compare the birth size (both unstandardized and standardized by gestational age) of individuals from OS pairs with that of individuals from SS pairs, we used linear regression models (twin type was used as the explanatory variable and birth size measures as the outcomes) adjusted for birth year and twin cohort separately by sex. The non-independence within twin pairs was taken into account by using the “cluster” option available in Stata. The association between twin pair type (boy-boy, boy-girl and girl-girl) and gestational age was analyzed using linear regression models (twin pair type was used as the explanatory variable and gestational age as the outcome variable) adjusted for birth year and twin cohort. To calculate the odds ratios (OR) for the risk of delivery at less than 37, 34 and 31 weeks (“preterm delivery” will be used as general term) between the three twin pair types, we used logistic regression models adjusted for birth year and twin cohort.

Finally, we compared gestational age between boys and girls separately by 7 birth weight classes of 0.5 kg (0.75–1.25, …, 3.75–4.25 kg) and 5 birth length classes of 5 cm (32.5–37.5, …, 52.5–57.5 cm). For these analyses, in addition to the exclusion of unrealistic birth size values for a given gestational age, we removed birth weight values <0.75 and ≥4.25 (n = 54) and birth length values <32.5 and ≥57.5 (n = 39) because the sample size was too small to create more categories. Linear regression models (sex was used as the explanatory variable and gestational age as the outcome variable) adjusted for birth year, twin cohort and non-independence within twin pairs were used.


Descriptive statistics for the three birth size measures of twin individuals in relation to the sex of their co-twin are presented in Table 1. The four twin type and sex groups had similar sample sizes ranging from 16,417 to 17,584 for birth weight and from 8,128 to 8,702 for birth length and PI. As expected, mean birth weight and length were greater in boys than in girls, with a difference of 83 g and 0.48 cm in SS twins and 111 g and 0.75 cm in OS twins, whereas PI was very similar in both sexes. Boys having a co-twin sister were, on average, 31 g (95% CI 18 to 45, p < 0.001) heavier and 0.16 cm (95% CI 0.045 to 0.274, p = 0.006) longer than those with a co-twin brother; however, PI at birth was similar in SS and OS twins. In girls, the sex of the co-twin was not associated with birth size.

We then compared mean gestational age and the risk of preterm delivery between twin pair types (boy-boy, boy-girl and girl-girl) (Table 2). Compared to boy-boy pairs, mean gestational age was greater in both boy-girl [0.13 weeks; 95% CI 0.06 to 0.21 (p = 0.001)] and girl-girl [(0.20 weeks; 95% CI 0.11 to 0.28 (p < 0.001)] pairs. In additional analyses using girl-girl pairs as the reference group (results not shown), gestational age was not significantly different between girl-girl and boy-girl pairs [−0.06 weeks; 95% CI −0.14 to 0.02 (p = 0.121)]. Further, both boy-girl and girl-girl pairs showed a lower risk (OR) of delivery before 37 weeks [0.92; 95% CI 0.86 to 0.98 (p = 0.007) and 0.88; 95% CI 0.82 to 0.95 (p = 0.001), respectively] and 34 weeks [0.89; 95% CI 0.81 to 0.99 (p = 0.024) and 0.80; 95% CI 0.71 to 0.90 (p = <0.001), respectively] than boy-boy pairs; a similar trend was observed for the risk before 31 weeks but did not reach statistical significance [0.88; 95% CI 0.73 to 1.06 (p = 0.165) and 0.82; 95% CI 0.66 to 1.02 (p = 0.078), respectively)]. Using girl-girl pairs as the reference group, boy-girl pairs showed slightly higher risk of delivery before 34 weeks [1.12; 95% CI 1.01 to 1.24 (p = 0.036)] than girl-girl pairs, but not before 37 weeks [1.04; 95% CI 0.97 to 1.11 (p = 0.291)] or 31 weeks [1.07; 95% CI 0.88 to 1.31 (p = 0.510)].

Table 2 Gestational age and risk of preterm delivery by dizygotic twin pair type (reference group boy-boy pairs).

In Table 3, we present the descriptive statistics and regression coefficients for the difference in gestational age standardized birth size measures of twins in relation to the sex of their co-twin. Birth weight was 0.028 z-score greater in OS than in SS twins of both sexes, that is, standardization by gestational age attenuated the magnitude of the association to half of the unstandardized value in boys and created a positive difference in girls. When regression coefficients were back-transformed to original values, maximum differences of 15 g in boys and 12 g in girls were observed. For birth length, the association was significant only in boys and the attenuation after the standardization by gestational age was modest; boys from OS pairs had 0.052 z-score (0.11–0.16 cm depending on gestational age) greater length than boys from SS pairs. In agreement with the unstandardized results, PI was not associated with the sex of the co-twin.

Table 3 Descriptive statistics and regression coefficients for the difference in gestational age standardized birth size of dizygotic twin boys and girls according to the sex of their co-twin (reference group same-sex dizygotic twins).

Figure 2 shows, per birth weight and length class, the difference of gestational age between boys from SS pairs (reference group) and boys from OS pairs, girls from OS pairs, and girls from SS pairs. For any given birth weight and length class, the gestational age of boys from SS pairs and boys from OS pairs was very similar. Gestation of girls was longer than that of boys for birth weights ranging between 0.75 kg and 3.75 kg and birth lengths ranging between 32.5 and 52.5 cm. The difference in gestational age between boys and girls was greatest for the smaller birth size classes and decreased with increasing birth weight and length from 2.5 kg and 45 cm classes.

Figure 2
Figure 2

Difference in gestational age (weeks) between individuals of the four twin type groups. Indicated weights and lengths are midpoint values of birth weight classes of 0.5 kg and 5 cm, respectively. B: regression coefficient for the difference in gestational age between sexes.


The present study, based on a multinational database of 21 twin cohorts from 15 countries, showed that birth weight and length are associated with the sex of the co-twin in boys. Differences in birth size between twins from SS and OS dizygotic twin pairs were of small magnitude and partly explained by differences in gestational age between boys and girls. Our results thus support the role of gestational age in the associations between co-twin’s sex and birth size and refine previous findings by considering, in addition to birth weight, also birth length and PI.

Boys with a co-twin sister were, on average, 31 g heavier at birth than those with a co-twin brother. Our findings are in line with previous studies showing a difference of 57 g10, 64 g11 and 78 g12, even when different inclusion criteria for SS twins were used. For girls, birth weight was very similar in SS and OS twins, which is also in agreement with these studies10,11,12. Boys with a co-twin sister were 0.16 cm longer than those with a co-twin brother, but differences were not significant in girls. Similar birth length in girls from SS and OS pairs was also observed in Canadian twins18. The lack of association of PI at birth with the sex of the co-twin may be because PI is a mathematical ratio of weight-to-length and proportional reduction in both birth weight and birth length will keep the ratio fairly unaffected. The attenuation of the associations between birth weight and co-twin’s sex after controlling for gestational age in boys was also observed in the study of Belgian twins12 (a part of this sample is included in the CODATwins project as the East Flanders Prospective Twin Survey), and has been attributed to a longer gestation in the presence of a co-twin sister.

Although Luke et al.16 found longer mean gestational age in OS pairs than in SS pairs in both sexes, our findings of shortest gestations in boy-boy pairs, intermediate in boy-girl pairs and longest in girl-girl pairs (36.6, 36.7 and 36.9 weeks, respectively) are in line with those observed in Belgian12 (36.4, 36.8 and 36.9 weeks, respectively) and Israeli11 (34.8, 35.1 and 35.2 weeks, respectively) twins. In the present study, the mean gestational ages between boy-girl and girl-girl pairs were not significantly different. Loos et al.12 reported a similar pattern for gestational age and concluded that it is the girl who governs the length of gestation, in such a way that there is a female-protective factor that prolongs gestation. However, Melamed et al.11 observed that mean gestational age and the risk of delivery before 31 and 28 weeks were significantly different between boy-girl and girl-girl pairs and they suggested that a potential “dose-dependent male-offending factor” might increase the risk of prematurity. Since in this multinational study the risk of delivery before 34 weeks was lower in girl-girl than in boy-girl pairs, this interpretation concerning a “dose-dependent male-offending factor” could also be applied to our results.

Although elucidating the mechanisms behind the association between the sex of the co-twin and birth size was not an objective of the present study, our results are opposite in direction to that predicted by the TTT hypothesis, at least in boys. We showed that gestational age has a role in the association between the co-twin’s sex and birth size. Melamed et al.11 speculated that the shortest gestational age in boy-boy pairs might be explained by the higher level of androgens in pregnancies with boys, which has been implicated in the onset of preterm labor28. Moreover, we do not know by which mechanisms, even after adjustment for gestational age, boys from OS pairs are significantly heavier and longer than boys from SS pairs. It has been suggested that, if the amount of nutrient available in boy-boy and boy-girl pregnancies are equal, boys in boy-girl pregnancies compared with those in boy-boy pregnancies will be more successful in the competition for nutrient because girls are programmed to grow slower29. However, girls from OS pairs were slightly heavier than those from SS pairs (after adjustment for gestational age), which is in opposite direction to the hypothesis of such maternal constraint. Moreover, and in agreement with previous studies in singletons22 and twins12, we showed that, to attain a given birth weight and length, the gestation of boys is shorter than that of girls, and the gestational age differences between boys and girls are smallest for the heaviest and longest children, which is not in accordance with this hypothesis either. This suggests that boys grow at a faster pace than girls, but that girls catch-up late in gestation. Pergament et al.30 found that female embryos, compared to male embryos, are already delayed in early embryonic development. It has been speculated that some critical time windows of development may be slightly different for boys and girls, and that this phenomenon may be one of the reasons for sex differences in sensitivity to fetal programming. In order to shed new light into the mechanisms behind the association between birth size and the co-twin’s sex, an interesting starting point for future studies would be to collect measures of fetal growth by ultrasound imaging at different stages of pregnancy to elucidate when these differences emerge.

The main strength of the present study is the large sample size of our multinational database of twin cohorts with information on birth weight, length and gestational age. We performed an individual-based pooled analysis to provide results for this sample including the large majority of existing twin cohorts having birth related measures. Generalization for the global population is, however, not possible because countries or regions are not equally represented and the database is heavily weighted towards European ancestry populations following westernized lifestyle. Another limitation of the data is that most of the measures were parentally reported27. However, the accuracy between reported birth weights and medical records of birth weights (in singletons) reached high kappa values (~0.90)31,32. Zygosity was also self-reported and not verified by DNA testing in the majority of studies. It is thus possible that misclassification of a small fraction of MZ twins as SS dizygotic twins could have contributed to part of the observed small differences in birth size between twin type groups. Finally, distinction between spontaneous and iatrogenic preterm birth (e.g. by caesarean section) is lacking.

We conclude from this multinational study that boys with a co-twin sister are heavier and longer at birth than those with a co-twin brother, but birth size in girls is not associated with the co-twin’s sex. The differences in boys are modest and partly explained by a longer gestation in the presence of a co-twin sister. Boy-boy pairs have a shorter length of gestation and a higher risk of preterm delivery than boy-girl and girl-girl pairs, and the difference in gestational age between boys and girls was generally smaller with greater birth size. Although the effects are too small to be of clinical significance, these findings have theoretical significance and might help to shed light on the underlying mechanisms linking birth size and the sex of the co-twin in future research.

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This study was conducted within the CODATwins project (Academy of Finland #266592).The Australian Twin Registry is supported by a Centre of Research Excellence (grant ID 1079102) from the National Health and Medical Research Council administered by the University of Melbourne.The Carolina African American Twin Study of Aging (CAATSA) was funded by a grant from the National Institute on Aging (grant 1RO1-AG13662-01A2) to K. E. Whitfield. The CATSS-Study is supported by the Swedish Research Council through the Swedish Initiative for Research on Microdata in the Social And Medical Sciences (SIMSAM) framework grant no 340-2013-5867, grants provided by the Stockholm County Council (ALF-projects), the Swedish Heart-Lung Foundation and the Swedish Asthma and Allergy Association’s Research Foundation. Since its origin the East Flanders Prospective Survey has been partly supported by grants from the Fund of Scientific Research, Flanders and Twins, a non-profit Association for Scientific Research in Multiple Births (Belgium). Data collection and analyses in Finnish twin cohorts have been supported by ENGAGE – European Network for Genetic and Genomic Epidemiology, FP7-HEALTH-F4-2007, grant agreement number 201413, National Institute of Alcohol Abuse and Alcoholism (grants AA-12502, AA-00145, and AA-09203 to R J Rose, the Academy of Finland Center of Excellence in Complex Disease Genetics (grant numbers: 213506, 129680), and the Academy of Finland (grants 100499, 205585, 118555, 141054, 265240, 263278 and 264146 to J Kaprio). Gemini was supported by a grant from Cancer Research UK (C1418/A7974). Anthropometric measurements of the Hungarian twins were supported by Medexpert Ltd., Budapest, Hungary. Longitudinal Israeli Study of Twins was funded by the Starting Grant no. 240994 from the European Research Council (ERC) to Ariel Knafo. The Michigan State University Twin Registry has been supported by Michigan State University, as well as grants R01-MH081813, R01-MH0820-54, R01-MH092377-02, R21-MH070542-01, R03-MH63851-01 from the National Institute of Mental Health (NIMH), R01-HD066040 from the Eunice Kennedy Shriver National Institute for Child Health and Human Development (NICHD), and 11-SPG-2518 from the MSU Foundation. The content of this manuscript is solely the responsibility of the authors and does not necessarily represent the official views of the NIMH, the NICHD, or the National Institutes of Health. PETS was supported by grants from the Australian National Health and Medical Research Council (grant numbers 437015 and 607358 to JC, and RS), the Bonnie Babes Foundation (grant number BBF20704 to JMC), the Financial Markets Foundation for Children (grant no. 032-2007 to JMC), and by the Victorian Government’s Operational Infrastructure Support Program. The Quebec Newborn Twin Study acknowledges financial support from the Fonds Québécois de la Recherche sur la Société et la Culture, the Fonds de la Recherche en Santé du Québec, the Social Science and Humanities Research Council of Canada, the National Health Research Development Program, the Canadian Institutes for Health Research, Sainte-Justine Hospital’s Research Center, and the Canada Research Chair Program (Michel Boivin). The Twins Early Development Study (TEDS) is supported by a program grant (G0901245) from the UK Medical Research Council and the work on obesity in TEDS is supported in part by a grant from the UK Biotechnology and Biological Sciences Research Council (31/D19086). Currently TEDS is supported by MRC grant ‘MR/M021475/1’. The West Japan Twins and Higher Order Multiple Births Registry was supported by Grant-in-Aid for Scientific Research (B) (grant number 15H05105) from the Japan Society for the Promotion of Science. Netherlands Twin Register acknowledges the Netherlands Organization for Scientific Research (NWO) and MagW/ZonMW grants 904-61-090, 985-10-002, 912-10-020, 904-61-193,480-04-004, 463-06-001, 451-04-034, 400-05-717, Addiction-31160008, Middelgroot-911-09-032, Spinozapremie 56-464-14192; VU University’s Institute for Health and Care Research (EMGO+); the European Research Council (ERC − 230374), the Avera Institute, Sioux Falls, South Dakota (USA).

Author information


  1. Department of Social Research, University of Helsinki, Helsinki, Finland

    • Aline Jelenkovic
    • , Reijo Sund
    •  & Karri Silventoinen
  2. Department of Genetics, Physical Anthropology and Animal Physiology, University of the Basque Country UPV/EHU, Leioa, Spain

    • Aline Jelenkovic
    •  & Esther Rebato
  3. Institute of Clinical Medicine, University of Eastern Finland, Kuopio, Finland

    • Reijo Sund
  4. Department of Public Health Nursing, Osaka City University, Osaka, Japan

    • Yoshie Yokoyama
  5. Department of Education, Mokpo National University, Jeonnam, South Korea

    • Yoon-Mi Hur
  6. Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden

    • Vilhelmina Ullemar
    • , Catarina Almqvist
    •  & Patrik KE Magnusson
  7. Pediatric Allergy and Pulmonology Unit at Astrid Lindgren Children’s Hospital, Karolinska University Hospital, Stockholm, Sweden

    • Catarina Almqvist
  8. Department of Biological Psychology, VU University Amsterdam, Amsterdam, Netherlands

    • Gonneke Willemsen
    • , Meike Bartels
    • , Catharina EM van Beijsterveldt
    •  & Dorret I. Boomsma
  9. Institute for Molecular Medicine FIMM, Helsinki, Finland

    • Leonie H. Bogl
    • , Eero Vuoksimaa
    •  & Jaakko Kaprio
  10. Department of Public Health, University of Helsinki, Helsinki, Finland

    • Leonie H. Bogl
    • , Eero Vuoksimaa
    •  & Jaakko Kaprio
  11. Obesity Research Unit, Research Programs Unit, University of Helsinki, Helsinki, Finland

    • Kirsi H Pietiläinen
  12. Endocrinology, Abdominal Center, Helsinki University Central Hospital and University of Helsinki, Helsinki, Finland

    • Kirsi H Pietiläinen
  13. Department of Noncommunicable Diseases Prevention, Qingdao Centers for Disease Control and Prevention, Qingdao, China

    • Fuling Ji
    • , Feng Ning
    •  & Zengchang Pang
  14. Department of Health and Exercise Sciencies and Colorado School of Public Health, Colorado State University, Fort Collins, USA

    • Tracy L Nelson
  15. Psychology and Neuroscience, Duke University, Durham, NC, USA

    • Keith E. Whitfield
  16. Health Behaviour Research Centre, Department of Epidemiology and Public Health, Institute of Epidemiology and Health Care, University College London, London, UK

    • Clare H. Llewellyn
    •  & Abigail Fisher
  17. Healthy Twin Association of Mongolia, Ulaanbaatar, Mongolia

    • Gombojav Bayasgalan
    •  & Danshiitsoodol Narandalai
  18. Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan

    • Danshiitsoodol Narandalai
  19. Bandim Health Project, INDEPTH Network, Bissau, Guinea-Bissau

    • Morten Bjerregaard-Andersen
  20. Research Center for Vitamins and Vaccines, Statens Serum Institute, Copenhagen, Denmark

    • Morten Bjerregaard-Andersen
  21. Department of Endocrinology, Odense University Hospital, Odense, Denmark

    • Morten Bjerregaard-Andersen
    •  & Henning Beck-Nielsen
  22. Department of Infectious Diseases, Odense University Hospital, Odense, Denmark

    • Morten Sodemann
  23. Department of Radiology, Semmelweis University, Budapest, Hungary

    • Adam D. Tarnoki
    •  & David L. Tarnoki
  24. Hungarian Twin Registry, Budapest, Hungary

    • Adam D. Tarnoki
    •  & David L. Tarnoki
  25. Department of Health Science, Ishikawa Prefectural Nursing University, Kahoku, Ishikawa, Japan

    • Syuichi Ooki
  26. Istituto Superiore di Sanità - Centre for Behavioural Sciences and Mental Health, Rome, Italy

    • Maria A. Stazi
    • , Corrado Fagnani
    •  & Sonia Brescianini
  27. School of Epidemiology, Public Health and Preventive Medicine, University of Ottawa, Ottawa, Ontario, Canada

    • Lise Dubois
  28. École de psychologie, Université Laval, Québec, Canada

    • Michel Boivin
    •  & Ginette Dionne
  29. Institute of Genetic, Neurobiological, and Social Foundations of Child Development, Tomsk State University, Tomsk, Russian Federation

    • Michel Boivin
  30. Département de psychologie, Université du Québec à Montréal, Montréal, Québec, Canada

    • Mara Brendgen
  31. École de psychoéducation, Université de Montréal, Montréal, Québec, Canada

    • Frank Vitaro
  32. The Australian Twin Registry, Centre for Epidemiology and Biostatistics, The University of Melbourne, Melbourne, Victoria, Australia

    • Tessa L Cutler
    •  & John L. Hopper
  33. Department of Epidemiology, School of Public Health, Seoul National University, Seoul, Korea

    • John L. Hopper
  34. Department of Psychology, University of Minnesota, Minneapolis, MN, USA

    • Robert F. Krueger
    • , Matt McGue
    •  & Shandell Pahlen
  35. Murdoch Childrens Research Institute, Royal Children’s Hospital, Parkville, Victoria, Australia

    • Jeffrey M. Craig
    •  & Richard Saffery
  36. Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia

    • Jeffrey M. Craig
    •  & Richard Saffery
  37. MRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK

    • Claire MA Haworth
  38. King’s College London, MRC Social, Genetic & Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, London, UK

    • Robert Plomin
  39. The Hebrew University of Jerusalem, Jerusalem, Israel

    • Ariel Knafo-Noam
    •  & Lior Abramson
  40. Hadassah Hospital Obstetrics and Gynecology Department, Hebrew University Medical School, Jerusalem, Israel

    • David Mankuta
  41. Michigan State University, East Lansing, Michigan, USA

    • S Alexandra Burt
    •  & Kelly L. Klump
  42. Centre of Human Genetics, University Hospitals Leuven, Leuven, Belgium

    • Robert F. Vlietinck
    •  & Catherine A. Derom
  43. Department of Obstetrics and Gynaecology, Ghent University Hospitals, Ghent, Belgium

    • Catherine A. Derom
  44. The Charles Bronfman Institute for Personalized Medicine, The Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA

    • Ruth JF Loos
  45. Novo Nordisk Foundation Centre for Basic Metabolic Research (Section of Metabolic Genetics), Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark

    • Thorkild I. A. Sørensen
  46. Department of Public Health (Section of Epidemiology), Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark

    • Thorkild I. A. Sørensen
  47. Osaka University Graduate School of Medicine, Osaka University, Osaka, Japan

    • Karri Silventoinen


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Y.Y., Y.-M.H., D.I.B., T.I.A.S., J.K. and K.S. planned the study design of the CODATwins project. Y.Y., V.U., C.A.M., P.K.E.M., G.W., M.B., C.E.M.v.B., L.H.B., K.P., E.V., F.J., F.N., Z.P., T.L.N., K.E.W., E.R., C.H.L., A.F., G.B., D.N., M.B.-A., H.B.-N., M.S., A.D.T., D.L.T., S.O., M.A.S., C.F., C.D., L.D., M.B.o., M.B.r., G.D., F.V., T.L.C., J.L.H., R.F.K., M.M., S.P., J.M.C., R.S., C.M.A.H., R.P., A.K.-N., D.M., L.A., S.A.B., K.L.K., R.F.V., C.A.D., R.J.F.L., D.I.B. and J.K. collected the data used in this study. A.J. and K.S. were in charge of data management. R.S. provided statistical advice. A.J. conducted the analyses and wrote the first draft of the manuscript. All authors have commented the manuscript and read and approved the final version of the manuscript.

Competing Interests

The authors declare no competing interests.

Corresponding author

Correspondence to Aline Jelenkovic.

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