Hostname: page-component-cd9895bd7-fscjk Total loading time: 0 Render date: 2024-12-25T01:49:03.878Z Has data issue: false hasContentIssue false
  • English
  • Français

The Mercurio Project and Twins. How to use a Registry

Published online by Cambridge University Press:  01 August 2014

R. Lanni ,
V. Grimaldi ,
C. Corchia  and
P. Mastroiacovo
R. Lanni
Affiliation:
International Center on Adverse Reproductive Outcomes - Italian Association for the Study of Malformations (ICARO-ASM)
V. Grimaldi
Affiliation:
International Center on Adverse Reproductive Outcomes - Italian Association for the Study of Malformations (ICARO-ASM)
C. Corchia
Affiliation:
Department of Pediatrics, University of Sassari
P. Mastroiacovo*
Affiliation:
Department of Pediatrics, Catholic University, Rome
*
Università Cattolica del Sacro Cuore, Clinica Pediatrica, Facoltà di Medicina e Chirurgia, Policlinico Universitario “A. Gemelli”, Largo Agostino Gemelli 8, 00168 Roma, Italia

Extract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

An essential element in any investigation of environment-genetics interaction is twin registries. At present there exist two types, one based on the whole population and another relying on voluntary participation. The second type is an important source of epidemiological information regarding the presence or absence of a disease (concordance) between members of monozygotic and dizygotic pairs. However, this type presents two serious drawbacks: the data do not cover all twins, and since the twins enrolled are those who require the greatest assistance, this results in a serious selection bias [2]. On the contrary, the first type has neither of these defects and represents an invaluable source of information for epidemiological studies on the concordance of pysiological features, morbidity and mortality, together with genetic and environmental influences and their interaction [1, 3-5].

April 1993 saw the first enrolment in a Multiple Pregnancies Registry designed to collect data from 47 Italian hospitals. This registry forms part of a larger survey, the “Mercurio Project”, originally set up in April 1992 under the aegis of the Italian Multicentre Birth Defects Registry (IPIMC). The aims of the registry are the following:

(a) to set up longitudinal epidemiological studies on the health, morbidity and mortality of twins

(b) to assess the role of environmental-genetic interaction in determining childhood behaviour and disease (using case-control studies where each twin is matched with his or her cotwin)

(c) to draw the attention of socio-sanitary personnel to twins and their special needs.

Type
Research Article
Information
Acta geneticae medicae et gemellologiae: twin research , Volume 43 , Issue 1-2 , April 1994 , pp. 95 - 103
Copyright
Copyright © The International Society for Twin Studies 1994

References

REFERENCES

1. Clifford, CA, Hopper, JL (1986): The Australian NHMRC twin registry. A resource for the Australian scientific community. Med J Australia 145:63–5.CrossRefGoogle ScholarPubMed
2. Hay, DA, Clifford, C, Derrick, P, Hopper, J. Renard, B, Theobald, TM (1990): Twin children in volunteer registries: biases in parental participation and reporting. Acta Genet Med Gemellol 39:71–84.Google ScholarPubMed
3. Kaprio, J, Koskenvuo, M, Rose, RJ (1990): Population-based twin registries: illustrative applications in genetic epidemiology and behavioral genetics from the Finnish twin cohort study. Acta Genet Med Gemellol 39:427–39.Google ScholarPubMed
4. Lykken, DT, Bouchard, TJ, McGue, M, Tellegen, A (1990): The Minnesota twin family registry: some initial findings. Acta Genet Med Gemellol 39:35–70.Google ScholarPubMed
5. Phillips, DIW (1993): Twin studies in medical research: can they tell us whether diseases are genetically determined? Lancet 341:1008–9.CrossRefGoogle ScholarPubMed