Scientific Reports (Oct 2021)
Vitamin D-related polymorphisms and vitamin D levels as risk biomarkers of COVID-19 disease severity
- Ana Teresa Freitas,
- Conceição Calhau,
- Gonçalo Antunes,
- Beatriz Araújo,
- Matilde Bandeira,
- Sofia Barreira,
- Filipa Bazenga,
- Sandra Braz,
- Daniel Caldeira,
- Susana Constantino Rosa Santos,
- Ana Faria,
- Daniel Faria,
- Marta Fraga,
- Beatriz Nogueira-Garcia,
- Lúcia Gonçalves,
- Pavlo Kovalchuk,
- Luísa Lacerda,
- Hugo Lopes,
- Daniel Luís,
- Fábio Medeiros,
- Ana M. P. Melo,
- José Melo-Cristino,
- Ana Miranda,
- Clara Pereira,
- Ana Teresa Pinto,
- João Pinto,
- Helena Proença,
- Angélica Ramos,
- João P. R. Rato,
- Filipe Rocha,
- Júlio César Rocha,
- André Moreira-Rosário,
- Helena Vazão,
- Yuliya Volovetska,
- João-Tiago Guimarães,
- Fausto J. Pinto
Affiliations
- Ana Teresa Freitas
- HeartGenetics, Genetics and Biotechnology SA
- Conceição Calhau
- Nutrition and Metabolism, NOVA Medical School, Universidade Nova de Lisboa
- Gonçalo Antunes
- HeartGenetics, Genetics and Biotechnology SA
- Beatriz Araújo
- Clinical Pathology Department, Centro Hospitalar Universitário de São João
- Matilde Bandeira
- Rheumatology Department, Hospital de Santa Maria, Centro Hospitalar Universitário Lisboa Norte, Centro Académico de Medicina de Lisboa
- Sofia Barreira
- Rheumatology Department, Hospital de Santa Maria, Centro Hospitalar Universitário Lisboa Norte, Centro Académico de Medicina de Lisboa
- Filipa Bazenga
- Clinical Pathology Department, Centro Hospitalar Universitário de São João
- Sandra Braz
- Internal Medicine Department, Santa Maria Hospital, Centro Hospitalar Universitário Lisboa Norte, Faculdade de Medicina da Universidade de Lisboa
- Daniel Caldeira
- Centro Cardiovascular da Universidade de Lisboa (CCUL), CAML, Faculdade de Medicina, Universidade de Lisboa
- Susana Constantino Rosa Santos
- Centro Cardiovascular da Universidade de Lisboa (CCUL), CAML, Faculdade de Medicina, Universidade de Lisboa
- Ana Faria
- Nutrition and Metabolism, NOVA Medical School, Universidade Nova de Lisboa
- Daniel Faria
- INESC-ID, Instituto Superior Técnico, University of Lisbon
- Marta Fraga
- Clinical Pathology Department, Hospital Santa Maria, Centro Hospitalar Universitário Lisboa Norte, EPE
- Beatriz Nogueira-Garcia
- Cardiology Department, Hospital Universitário de Santa Maria - CHULN
- Lúcia Gonçalves
- HeartGenetics, Genetics and Biotechnology SA
- Pavlo Kovalchuk
- HeartGenetics, Genetics and Biotechnology SA
- Luísa Lacerda
- Clinical Pathology Department, Centro Hospitalar Universitário de São João
- Hugo Lopes
- HeartGenetics, Genetics and Biotechnology SA
- Daniel Luís
- HeartGenetics, Genetics and Biotechnology SA
- Fábio Medeiros
- Infectious Disease Department, Santa Maria Hospital - CHULN
- Ana M. P. Melo
- Portuguese Infrastructure of Biological Data – BioData.pt
- José Melo-Cristino
- Clinical Pathology Department, Hospital Santa Maria, Centro Hospitalar Universitário Lisboa Norte, EPE
- Ana Miranda
- Clinical Pathology Department, Hospital Santa Maria, Centro Hospitalar Universitário Lisboa Norte, EPE
- Clara Pereira
- HeartGenetics, Genetics and Biotechnology SA
- Ana Teresa Pinto
- Centro Cardiovascular da Universidade de Lisboa (CCUL), CAML, Faculdade de Medicina, Universidade de Lisboa
- João Pinto
- Clinical Pathology Department, Centro Hospitalar Universitário de São João
- Helena Proença
- Clinical Pathology Department, Hospital Santa Maria, Centro Hospitalar Universitário Lisboa Norte, EPE
- Angélica Ramos
- Clinical Pathology Department, Centro Hospitalar Universitário de São João
- João P. R. Rato
- Portuguese Infrastructure of Biological Data – BioData.pt
- Filipe Rocha
- Centro Cardiovascular da Universidade de Lisboa (CCUL), CAML, Faculdade de Medicina, Universidade de Lisboa
- Júlio César Rocha
- Nutrition and Metabolism, NOVA Medical School, Universidade Nova de Lisboa
- André Moreira-Rosário
- Nutrition and Metabolism, NOVA Medical School, Universidade Nova de Lisboa
- Helena Vazão
- HeartGenetics, Genetics and Biotechnology SA
- Yuliya Volovetska
- Clinical Pathology Department, Hospital Santa Maria, Centro Hospitalar Universitário Lisboa Norte, EPE
- João-Tiago Guimarães
- Clinical Pathology Department, Centro Hospitalar Universitário de São João
- Fausto J. Pinto
- Centro Cardiovascular da Universidade de Lisboa (CCUL), CAML, Faculdade de Medicina, Universidade de Lisboa
- DOI
- https://doi.org/10.1038/s41598-021-99952-z
- Journal volume & issue
-
Vol. 11,
no. 1
pp. 1 – 8
Abstract
Abstract Vitamin D is a fundamental regulator of host defences by activating genes related to innate and adaptive immunity. Previous research shows a correlation between the levels of vitamin D in patients infected with SARS-CoV-2 and the degree of disease severity. This work investigates the impact of the genetic background related to vitamin D pathways on COVID-19 severity. For the first time, the Portuguese population was characterized regarding the prevalence of high impact variants in genes associated with the vitamin D pathways. This study enrolled 517 patients admitted to two tertiary Portuguese hospitals. The serum concentration of 25 (OH)D, was measured in the hospital at the time of patient admission. Genetic variants, 18 variants, in the genes AMDHD1, CYP2R1, CYP24A1, DHCR7, GC, SEC23A, and VDR were analysed. The results show that polymorphisms in the vitamin D binding protein encoded by the GC gene are related to the infection severity (p = 0.005). There is an association between vitamin D polygenic risk score and the serum concentration of 25 (OH)D (p = 0.04). There is an association between 25 (OH)D levels and the survival and fatal outcomes (p = 1.5e−4). The Portuguese population has a higher prevalence of the DHCR7 RS12785878 variant when compared with its prevalence in the European population (19% versus 10%). This study shows a genetic susceptibility for vitamin D deficiency that might explain higher severity degrees in COVID-19 patients. These results reinforce the relevance of personalized strategies in the context of viral diseases. Trial registration: NCT04370808.