| Literature DB >> 30985857 |
Lavinia Schüler-Faccini1, Maria Teresa Vieira Sanseverino1, Alberto Mantovani Abeche1, Fernanda Sales Luiz Vianna1, Lucas Rosa Fraga1, Anastacia Guimaraes Rocha1, André Anjos da Silva1, Paulo Ricardo Assis de Souza1, Artur Hartmann Hilgert1, Camila Pocharski Barbosa1, Caroline Grasso Kauppinem1, Daniela Fernandes Martins1, Daniela Silva Santos1, Gabriel Henrique Colpes1, Gabriela Ecco1, Helena Margot Flores Soares da Silva1, Louise Piva Penteado1, Tatiane Dos Santos1.
Abstract
In 1990, the first Teratogen Information Service in Brazil (SIAT) was implemented in the Medical Genetics Service at Hospital de Clinicas de Porto Alegre. SIAT is a free-to-use information service both to health professionals and the general population, especially to women who are pregnant or planning pregnancy. The main objective of this paper is to present the activities of SIAT in its initial years (1990-2006), compared to those in the last decade (2007-2017). In addition we review the scientific contribution of SIAT in the field of human teratogenesis. Since 1990, SIAT received 10,533 calls. Use of medications were the main reason for concern, accounting for 74% of all questions, followed by other chemical exposures (occupational, cosmetics, environmental), and maternal infectious diseases. Among its main contributions to scientific knowledge was the collaboration for the identification of two new human teratogens: misoprostol in the 1990s and Zika virus in 2015/16. In conclusion, SIAT is still evolving, as is the Medical Genetics Service that hosts it. Through its 27 years of existence more than 300 undergraduate and graduate students have rotated at SIAT. Presently, SIAT is expanding the research to experimental teratogenesis and to investigation of molecular mechanisms of teratogens.Entities:
Year: 2019 PMID: 30985857 PMCID: PMC6687353 DOI: 10.1590/1678-4685-GMB-2018-0111
Source DB: PubMed Journal: Genet Mol Biol ISSN: 1415-4757 Impact factor: 1.771
Profile of index cases and callers in the two different periods.
| 1990-2006 (Total N = 6503) | 2007-2017 (Total N = 4030) | |
|---|---|---|
| N(%) | N(%) | |
|
| ||
| Pregnant women | 3891 (64.47) | 1974 (50.81) |
| Researchers | 685 (11.35) | 436 (11.22) |
| Women planning pregnancy | 661 (10.95) | 910 (23.42) |
| Child with congenital defect | 517 (8.57) | 316 (8.13) |
| Paternal exposures | 165 (2.73) | 111 (2.86) |
| Use of medications during lactation | 116 (1.92) | 138 (3.55) |
|
| ||
| Medical Doctor | 3200 (49.21) | 2370 (67.39) |
| Index women | 2181 (33.54) | 908 (25.82) |
| Researchers | 685 (10.53) | 80 (2.27) |
| Other professionals | 267 (4.11) | 159 (4.52) |
| Husband / Relative | 170 (2.61) | 0 (0.0) |
Number of valid cases: n = 6035 between 1990-2006 and n = 3885 between 2007-2017;
p-value < 0.0001;
Number of valid cases: n = 6503 between 1990-2006 and n = 3517 between 2007-2017;
p-value < 0.0001.
Demographic characteristics of the index women
| 1990-2006 | 2007-2017 | |
|---|---|---|
| N (%) | N (%) | |
|
| ||
| South | 3097 (68.07) | 1913 (61.12) |
| Other Regions | 1374 (30.20) | 1195 (38.18) |
| Other Countries | 79 (1.74) | 22 (0.70) |
|
| ||
| Illiterate | 17 (0.43) | 1 (0.06) |
| Incomplete Elementary School | 236 (5.91) | 32 (2.01) |
| Elementary School | 513 (12.85) | 58 (3.65) |
| High School | 1556 (38.98) | 389 (24.47) |
| Academic Degree | 1670 (41.83) | 1110 (69.81) |
|
| ||
| < 20 | 262 (5.59) | 52 (1.97) |
| 20 - 34 | 3317 (70.79) | 1677 (63.38) |
| > 35 | 1107 (23.62) | 917 (34.66) |
Number of valid cases: n = 4550 between 1990-2006 and n = 3130 between 2007-2017;
p-value < 0.0001;
Number of valid cases: n = 3992 between 1990-2006 and n = 1590 between 2007-2017;
p-value < 0.0001;
Number of valid cases: n = 4686 between 1990-2006 and n = 2646 between 2007-2017;
p-value < 0.0001.
Reasons for Calls (Exposures)[a].
| 1990-2006 (Total N = 12486) | 2007-2017 (Total N = 7979) | |
|---|---|---|
| N (%) |
| |
| Medications | 9360 (74.96) | 5930 (74.32) |
| CNS[ | 2282 (24.40) | 2784 (46.95) |
| Anti-infective | 1231 (13.10) | 513 (8.65) |
| Painkiller | 681 (7.30) | 233 (3.93) |
| Inducing-Abortion Substances | 394 (4.20) | 48 (0.81) |
| Other substances (Occupational, hair dye, pesticides, etc.) | 1367 (10.95) | 670 (8.40) |
| Infections and Vaccines | 611 (4.89) | 245 (3.07) |
| Radiation | 491 (3.93) | 163 (2.04) |
| Smoking/Alcohol/Recreational Drugs | 234 (1.87) | 152 (1.91) |
| Advanced Maternal Age | 60 (0.48) | 6 (0.08) |
| Congenital Malformations | 58 (0.46) | 11 (0.14) |
| Maternal Diseases (excluding infections) | 51 (0.41) | 92 (1.15) |
| Consanguinity | 15 (0.12) | 3 (0.04) |
p-value < 0.0001;
Main classes of medications;
p-value < 0.0001. CNS: Central nervous system.
Selected SIAT studies and its contribution to the field of human teratogenesis.
| Exposure | Type of study | Main findings | Author, year |
|---|---|---|---|
|
| |||
| Thalidomide | Case series | Description of three cases of TE occurred in Brazil after 2005. |
|
| Pharmacovigilance | Hospital-based epidemiological surveillance. |
| |
| Case series | Description of two cases of TE in regions with a high prevalence of leprosy and the development of a checklist for recognition of TE phenotypes. |
| |
| Case series | Follow-up of TE cases born between 1959 and 2010. |
| |
| Pharmacovigilance | Hospital-based epidemiological surveillance. |
| |
| Molecular | Analyses of genetic variants related to TE. |
| |
| Review | History of thalidomide use in Brazil and the occurrence of new cases of TE. |
| |
| Misoprostol | Case-control | Misoprostol associated to the occurrence of Moebius sequence in newborns exposed to the medication during pregnancy. |
|
| Case-control | Misoprostol associated to the occurrence of defects of vascular disruption in newborns. |
| |
| Venlafaxine | Prospective multicentre cohort | No evidences of increased risk for major malformations. |
|
| Loratadine | Prospective multicentre cohort | No association for increased risk for major malformations. |
|
|
| |||
| Rubella Vaccine | Prospective cohort | Vaccine safety during pregnancy, presenting no risk for congenital anomalies. |
|
| H1N1 virus and oseltamivir | Prospective cohort | No increased risk for major anomalies in exposures to H1N1 or oseltamivir. |
|
| Zika Virus | Case series | Suggestion of a possible association between maternal infection by Zika virus and congenital microcephaly. |
|
| Critical Review | Discussion and confirmation of Zika virus as a new human teratogen. |
| |
| Case series | Description of 1501 newborns with congenital microcephaly in Brazil. |
| |
| Critical Review | Contribution in the definition of criteria for notification of microcephaly in Brail. |
| |
| Case series | Description of the phenotype of Zika virus embryopathy. |
| |
|
| Hospital-based | No association for increased risk for major malformations. |
|
| Hospital-based | No association for increased risk for major malformations and other adverse outcomes. |
| |
|
| Case-control | Association between maternal alcohol use during pregnancy and criminal behavior |
|
| Review | Evaluation of teratogens in the Brazilian population. |
| |
| Review and evaluation of congenital anomalies in Brazil | Integrative approach of the principles of teratogenesis, teratogenic mechanisms, and other aspects. |
|