Access to genetic evaluation of 1463 individuals with orofacial cleft in BrazilAbstract
Objective The current study delves into the accessibility of genetic evaluations for individuals with orofacial clefts (OC), comparing data between genetics and treatment centers across Brazil.
Methods This cross-sectional retrospective study analyzed primary data from 1463 OC individuals registered in the Brazilian Database of Craniofacial Anomalies (BDCA) between 2008 and 2018 without age or sex selection. Diagnostic exam results stemming from research projects until 2023 were considered.
Results Of the 1463 individuals with typical OC, 987 were non-syndromic, 462 were syndromic (SOC), 10 presented atypical forms, and three were not specified OC cases. The average age for accessing laboratory diagnosis was 8.5 years among SOC individuals. Notably, more SOC cases were registered in genetics centers than treatment and rehabilitation centers (37.1 % vs. 29 %, p = 0.0015). Those originating from genetics centers accessed diagnosis at an average age of 7.3 years, while those from treatment and rehabilitation centers experienced delays with an average age of 10.7 years (p = 0.0581).
Conclusions Irrespective of the center of origin, the data highlight delayed diagnosis and challenges in accessing genetic tests for the syndromic group. Given the widespread reliance on the public health system by most of the Brazilian population, disseminating this data can significantly contribute to shaping an informed perspective on healthcare access. These insights can improve public policies tailored to the unique needs of individuals with OC.
Keywords Orofacial cleft; Genetic services; Public health; Cleft lip; Cleft palate
Introduction
Orofacial clefts (OC), impacting approximately 4.24/10.000 live births in Brazil,1 present considerable challenges to affected individuals, compromising aesthetics and functional aspects of life. The complex etiology of OC involves isolated cases influenced by genetic and environmental factors, while syndromic cases typically arise from Mendelian variants, chromosomal alterations and imbalances, and teratogenesis;2 unknown causes still represent a significant part of these cases.
The World Health Organization emphasizes a holistic approach to OC cleft care, necessitating collaboration among different specialties, which includes medical genetic services.3 In Brazil, public hospitals play a pivotal role in cleft lip and palate correction and rehabilitation, with 30 accredited centers nationwide.4 However, it is notable that medical geneticists are not mandatory within them.5
Individuals with OC often undergo genetic evaluation and testing at universities or specialized rare disease centers in Brazil. The National Policy for Comprehensive Care for People with Rare Diseases (PNAIPDR), initiated in 2014, advocates for integral and coordinated care within the Brazilian public health system.6 Unfortunately, financial constraints, outdated resource allocations, and a scarcity of reference centers in certain states contribute to a substantial backlog of patients awaiting genetic testing.7
In 2003, Brazil's Craniofacial Project (BCFP) emerged at Universidade Estadual de Campinas (Unicamp), focusing on individuals with craniofacial anomalies (CFA) and operating on three fronts—health care, genetics of OC and specific conditions, and education. The BCFP, with 12 voluntary participating centers, has significantly contributed to molecular diagnosis, genetic counseling, and insights informing public policies.8-13 All patient data is voluntarily recorded at the Brazilian Database of Craniofacial Anomalies (BDCA).
In the complex landscape of genetic access for individuals with OC in Brazil, this study seeks to assess the accessibility of diagnostic services for those with these conditions. By comprehensively understanding the existing scenario, the research aims to provide insights to guide potential improvements in genetic services and enhance overall orofacial cleft care in Brazil.
Methodology
This is a descriptive cross-sectional study focused on analyzing primary data obtained from 1463 individuals with OC. Data were collected during the period spanning from 2008 to 2018. Inclusion criteria encompassed registration with the BDCA, the presence of an orofacial cleft, and comprehensive records of clinical information. There were no age restrictions or sex specifications for inclusion in the study. Exclusion criteria included incomplete/inconsistent data records.
The results of genetic tests carried out until 2023 were included. All data originated from the BDCA and were cross-referenced with the BCFP.
The participating centers within the BCFP were categorized into genetic and rehabilitation/treatment centers; all had genetic evaluations. From the nine centers participating in this study, four were classified as genetic centers and three as rehabilitation/treatment. Two centers could not be classified in any of these categories, and therefore, patients from both were not counted for comparative purposes between genetics and rehabilitation/treatment centers.
The collected data were categorized into sociodemographics, clinics, and information about access to diagnostics. Most diagnostic examinations were conducted within the research framework of BCFP at Unicamp, utilizing methods such as Fluorescence in situ hybridization (FISH), Multiplex ligation-dependent probe amplification (MLPA), Chromosomal microarray analysis (CMA), and whole exome sequencing. The only exception is karyotyping, which may have occurred within the Brazilian public or private health system. The age of access to diagnosis corresponded to the date of registration with the BBAC, capturing sociodemographic and clinical data. Individuals who were diagnosed under one year of age had their age at diagnosis changed to zero. Sociodemographic data was not complete for all individuals participating in the study. Therefore, some information has a total number of individuals lower than the total sample.
This study was approved by the Ethics Committee Board of the Universidade Estadual de Campinas (Unicamp), CAAE: 35316314.9.1001.5404 and 5020018.8.0000.5404 and in all participant centers.
All participants or their legal guardians signed the informed consent form.
Statistical analysis
Descriptive analysis was performed for categorical and numerical variables. When necessary, the Chi-square test, Fisherʼs exact test, or the Mann-Whitney test was applied to compare proportions and groups. The significance level adopted for statistical tests was p < 0.005.
Results
Sociodemographic data of the casuistry
In total, 1463 individuals with OC were included in this study. The majority were male, aged under six, and from the Northeast. Their sociodemographic aspects are described in Table 1.
Orofacial clefts classification
The OC observed in this study were classified as typical non-syndromic (NSOC), typical syndromic (SOC), atypical, or not specified. Subsequently, these were classified according to their topographic location as cleft lip, lip and palate, cleft palate, bifid uvula, or atypical OC (Table S1, Supplementary material).
Orofacial clefts diagnosis
Usually, NSOC diagnosis is essentially made by dysmorphological evaluation and genetic tests are not necessary. A specific diagnosis for atypical and not specified OC individuals was unavailable at BDCA. Data regarding access to diagnosis among the 462 individuals with SOC are described in Table 2.
Genetic centers versus treatment/rehabilitation centers
In total, it was possible to classify the center of origin of 1343 individuals. Among these, 491 (36.6 %) came from genetics centers and 852 (63.4 %) from treatment/rehabilitation. The proportion of the different types of OC according to their classification concerning the center of origin can be seen in Table 3.
The proportion of individuals with syndromic orofacial cleft who were diagnosed clinically and by genetic testing concerning the centers of origin are described in Table 4.
Discussion
This study reflects the BCFP/BDCA strategy to address the gap in access to genetic evaluation and diagnostic testing for OC among its participant centers. Therefore, the geographical distribution of individuals, type, or topographic location of OC recorded does not reflect an epidemiological pattern, nor the absence of OC diagnosis in the North and Central West regions. The composition of the sample group aligns with the prevailing distribution observed in the literature concerning individuals with SOC and NSOC.14
Of the 462 individuals with SOC, 28.6 % received a diagnosis. Although a notable proportion (51.5 %) received a molecular diagnosis, the mean age of molecular diagnosis was 8.5 years. In contrast, access to clinical diagnosis occurred approximately two times earlier for 48.5 % of individuals who obtained it.
This temporal contrast between access to clinical versus molecular diagnosis underscores the challenges of accessing genetic tests in Brazil. The limitations within the public health system, including restricted funding for genetic testing, a scarcity of genetic services, and delays in the arrival of patients at the reference service, contribute to this disparity.7,13,15-18 Conversely, while offering genetic testing, private healthcare still needs to be financially accessible for most of the Brazilian population.19
Acting voluntarily and with resources from research funding agencies, the BCFP incorporates a small group of patients, as they are included in research projects. These limitations do not allow all individuals referred for clinical follow-up at BCFP to access genetic testing.12
In this context, revising the standards for OC public service accreditation with the inclusion of medical genetics (for evaluation and genetic tests) or establishing consistent interaction with the PNAIPDR would benefit the Brazilian public OC care policy. This strategic measure aims to enhance and speed up identifying potential diagnoses, ensuring swift referrals to more targeted genetic tests.
Regarding the disproportion between syndromic individuals coming from genetics centers versus treatment/rehabilitation centers, it is essential to mention that, most likely, when there is a genetic center close to where the person with SOC resides, there is a greater probability that they will be referred further quickly to these centers to define the diagnosis. When there are only treatment/rehabilitation centers, the referral of people with SOC can be directed, preferably, to centers specializing in rare genetic diseases.
For instance, within the cohort of individuals with SOC originating from rehabilitation/ treatment centers, the average age of molecular diagnosis obtained was 10.7 years, contrasting with 7.3 years in genetic centers. Even so, it is noteworthy that all genetic tests were carried out within the BCFP. Ensuring timely access to genetic services is crucial in streamlining genetic counseling and providing comprehensive clinical follow-up for patients.20 These data underscore the indispensable role of geneticists in this domain.
The results show that the age at which individuals with syndromic orofacial cleft access diagnostic tests is late but similar to what is observed for rare diseases in Brazil.21 The current scenario reinforces a critical need for interventions to improve the accessibility of genetic testing, particularly within the public health system. This study underscores the importance of advocating for enhanced resources, increased distribution of genetic services, and reduced financial barriers to ensure comprehensive care for this population. Specifically for oral clefts, targeted public policies involving genetic evaluation and diagnosis can increase health care.
Data availability of data and statement
The datasets generated and analyzed during the current study are not publicly available because they contain personal information from patients.
Acknowledgments
The authors would like to record the gratitude to the families recorded at BDCA. The authors are also indebted to Professor Raquel T. Boy da Silva, from Pedro Ernesto University Hospital, State University of Rio de Janeiro, RJ, Brazil, and Professor Adriana Augusto de Rezende from the Department of Clinical and Toxicological Analysis, School of Pharmaceutical Sciences; Hospital Onofre Lopes (HUOL), Federal University of Rio Grande do Norte (UFRN), Natal, RN, Brazil for their participating in Brazil's Craniofacial Project.
Supplementary materials
Supplementary material associated with this article can be found in the online version at doi:10.1016/j.jped.2024.07.002.
-
Funding statement
This work received funding from the National Council for Scientific and Technological Development—CNPq [#140354/2020-4; #309782/2020-1 and 304684/2023-6]. The Postgraduate Program in Medical Sciences is supported by Coordination for the Improvement of Higher Education Personnel—CAPES [# 001].
References
- 1 Drizlionoks E., Klein C. Perfil clínico-epidemiológico da genética médica no Sistema Único de Saúde : análise do município de São Carlos, SP clinical and epidemiological profile of medical genetics in the single health. Medicina (B Aires). 2010;7:4-15.
- 2 E.J. Leslie and M.L. Marazita. Genetics of cleft lip and cleft palate. Am J Med Genet C Semin Med Genet 2013;163:246-58.
- 3 World Health Organization. Global Strategies to Reduce the Health-Care Burden of Craniofacial anomalies: Report of WHO Meetings on International Collaborative Research on Craniofacial Anomalies, Geneva, Switzerland, 5-8 November 2000; Park City, utah, U.S.A., 24-26 May 2001. World Health. 2002:1-148.
-
4 Brasil, Ministério da Saúde. Centros de tratamento da má formação lábio palatal 2020. [Cited Mar 26 2024]. Available from: http://cnes2.datasus.gov.br/Mod_Ind_Habilitacoes_Listar.asp?VTipo=0401&VListar=1&VEstado=00&VMun=&VComp=&VContador=30&VTitulo=H
» http://cnes2.datasus.gov.br/Mod_Ind_Habilitacoes_Listar.asp?VTipo=0401&VListar=1&VEstado=00&VMun=&VComp=&VContador=30&VTitulo=H - 5 Monlleó I.L., Gil-Da-Silva-Lopes V.L. Brazil's craniofacial project: genetic evaluation and counseling in the reference network for craniofacial treatment. Cleft Palate-Craniofac J. 2006;43:577-9.
- 6 Ministério da Saúde. Diretrizes para Atenção Integral às Pessoas com Doenças Raras no Sistema Único de Saúde - SUS. Portaria no 199, 30 janeiro 2014 2014:41. Brasília, 2014.
- 7 Interfarma. Avanços e Desafios na implementação da Portaria GM/MS No 199/2014 no Sistema Único de Saúde (SUS). 2021:1-55.
- 8 Sgardioli I.C., de Mello C.M., Monteiro F., dos Santos A.P., Lustosa M.E., Paiva Vieira T., et al. Diagnostic approach to microdeletion syndromes based on 22q11.2 investigation: challenges in four cases. Mol Syndromol. 2017;8:244-52.
- 9 Monlleó I.L., Ítalo M., Fontes B., Ribeiro E.M., de Souza J., Leal G.F., et al. Implementing the Brazilian database on orofacial clefts 2013; Plast Surg Int. 2013;2013:641570.
- 10 Sgardioli I.C., Vieira T.P., Simioni M., Monteiro F.P., Gil-da-Silva-Lopes V.L. 22q11.2 deletion syndrome: laboratory diagnosis and TBX1 and FGF8 mutation screening. J Pediatr Genet. 2015;4:17-22.
- 11 Volpe-Aquino R.M., Monlleó I.L., Lustosa-Mendes E., Mora A.F., Fett-Conte A.C., Félix T.M., et al. CranFlow: an application for record-taking and management through the brazilian database on craniofacial anomalies. Birth Defects Res. 2018;110:72-80.
- 12 Gil-da-silva-lopes V.L., Tacla M.A., Sgardioli I.C., Vieira T.P., Monlleó IL. Brazil ’ s craniofacial project : different approaches on orofacial clefts and 22q11. 2 deletion syndrome. Am J Med Genet. 2020:1-16.
- 13 Gil-da-Silva-Lopes V.L., Fontes M.I.B., dos Santos A.P., Appenzeller S., Fett-Conte A.C., Francisquetti M.C.C., et al. Syndromic oral clefts: challenges of genetic assessment in Brazil and suggestions to improve health policies. Public Health Genomics. 2019; 887:1-7.
- 14 Mossey P.A., Modell B. Epidemiology of oral clefts 2012 : an international perspective. Front Oral Biol. 2012;16:1-18.
- 15 Gandelman H.D., de Faria F.V., Dain S., Marques-de-Faria AP. Genetic services and testing in Brazil. J Community Genet. 2013;4:355-75.
- 16 Passos-Bueno M.R., Bertola D., Horovitz D.D., de Faria F.V., Brito L.A. Genetics and genomics in Brazil: a promising future. Mol Genet Genomic Med. 2014;2:280-91.
- 17 Phillips K.A., Deverka P.A., Hooker G.W., Douglas M.P. Genetic test availability and spending: where are we now? Where are we going? Health Aff. 2018;37:710-6.
- 18 de Oliveira B.M., Neiva M.B., Carvalho I., Schwartz I.V., Alves D., Felix T.M. Availability of genetic tests in public health services in Brazil: data from the Brazilian rare diseases network. Public Health Genomics. 2023:145-58.
- 19 IBGE - Instituto Brasileiro de Geografia e Estatística. Pesquisa Nacional de Saúde 2019: informações sobre domicílios, acesso e utilização dos serviços de saúde. 2019.
- 20 Gil-da-Silva-Lopes V.L., Monlleó IL. Risk factors and the prevention of oral clefts. Braz Oral Res. 2014;28:1-5.
-
21 Rede Raras. Cenário de Doenças Raras no Brasil; 2024. [Cited Mar 26 2024]. Available from: https://apps.raras.org.br:8502/
» https://apps.raras.org.br:8502/
Publication Dates
-
Publication in this collection
29 Nov 2024 -
Date of issue
2024
History
-
Received
26 Mar 2024 -
Accepted
1 July 2024 -
Published
22 July 2024
