Risk‐mitigating behaviours in people with inflammatory skin and joint disease during the COVID‐19 pandemic differ by treatment type: a cross‐sectional patient survey*
Abstract:Background Registry data suggest that people with immune-mediated inflammatory diseases (IMIDs) receiving targeted systemic therapies have fewer adverse coronavirus disease 2019 (COVID-19) outcomes compared with patients receiving no systemic treatments. Objectives We used international patient survey data to explore the hypothesis that greater risk-mitigating behaviour in those receiving targeted therapies may account, at least in part, for this observation. Methods Online surveys were completed by individual… Show more
“…It has been shown that people with psoriasis receiving targeted biological and systemic therapies are likely to follow the most stringent risk-mitigating behaviours. 5 In conclusion, psoriasis and AE were not associated with an increased risk of testing positive for COVID-19. On this evidence, it appears that psoriasis and AE should not be considered as risk factors for contracting COVID-19.…”
mentioning
confidence: 82%
“…C. Pan, 1,2 A. Humbatova, 3 L. Zheng, 1,2 N. Cesarato, 3 C. Grimm, 4 F. Chen, 1,2 B. Blaumeiser, 5 A. Catal an-Lamb an, 6 A. Patiño-Garc ıa, 6 U. Fischer, 4 R. Cheng, 1 Y. Li, 1,2 X. Yu, 1 Z. Yao iD , 1,2 M. Li iD 1,2,7 and R.C. Betz iD 3…”
which affects the start codon of SNRPE. This variant was associated with HHS in our original study. 3 The fact that we identified mutations in three ethnically diverse families suggests that mutations in SNRPE are a relatively frequent occurrence. It is thus surprising that no additional cases have been reported since our original publication. 3 As also observed in the cases at that time, there was wide phenotypic variation in the present ones.Concerning the splice site mutation, c.54+2T>A directly affects one of the most conserved nucleotides of the 5 0 splice site of intron 1. As the newly activated splice site donor, which allows exon 1 skipping, was found in the vector sequence, we cannot exclude the possibility that another mechanism is taking place in vivo. However, if the described aberrant transcript were to be produced, it may be either subjected to RNA decay or, more likely, allow the production of an in-frame 52 amino acid-long protein corresponding to a different small nuclear ribonucleoprotein polypeptide E (SNRPE) isoform (ENST00000 367208Á1). We suggest that the lower expression of wildtype protein, or the imbalance between the two isoforms, impacts on SNRPE function with respect to hair growth/ development. 3 Interestingly, a mutation in SNRPE was recently identified in a patient with primary microcephaly and intellectual disability. 2 None of the present cases showed either clinical feature. This study identified two novel heterozygous mutations, and one known mutation, in SNRPE. This expands the mutational and ethnic spectrum of HHS.
“…It has been shown that people with psoriasis receiving targeted biological and systemic therapies are likely to follow the most stringent risk-mitigating behaviours. 5 In conclusion, psoriasis and AE were not associated with an increased risk of testing positive for COVID-19. On this evidence, it appears that psoriasis and AE should not be considered as risk factors for contracting COVID-19.…”
mentioning
confidence: 82%
“…C. Pan, 1,2 A. Humbatova, 3 L. Zheng, 1,2 N. Cesarato, 3 C. Grimm, 4 F. Chen, 1,2 B. Blaumeiser, 5 A. Catal an-Lamb an, 6 A. Patiño-Garc ıa, 6 U. Fischer, 4 R. Cheng, 1 Y. Li, 1,2 X. Yu, 1 Z. Yao iD , 1,2 M. Li iD 1,2,7 and R.C. Betz iD 3…”
which affects the start codon of SNRPE. This variant was associated with HHS in our original study. 3 The fact that we identified mutations in three ethnically diverse families suggests that mutations in SNRPE are a relatively frequent occurrence. It is thus surprising that no additional cases have been reported since our original publication. 3 As also observed in the cases at that time, there was wide phenotypic variation in the present ones.Concerning the splice site mutation, c.54+2T>A directly affects one of the most conserved nucleotides of the 5 0 splice site of intron 1. As the newly activated splice site donor, which allows exon 1 skipping, was found in the vector sequence, we cannot exclude the possibility that another mechanism is taking place in vivo. However, if the described aberrant transcript were to be produced, it may be either subjected to RNA decay or, more likely, allow the production of an in-frame 52 amino acid-long protein corresponding to a different small nuclear ribonucleoprotein polypeptide E (SNRPE) isoform (ENST00000 367208Á1). We suggest that the lower expression of wildtype protein, or the imbalance between the two isoforms, impacts on SNRPE function with respect to hair growth/ development. 3 Interestingly, a mutation in SNRPE was recently identified in a patient with primary microcephaly and intellectual disability. 2 None of the present cases showed either clinical feature. This study identified two novel heterozygous mutations, and one known mutation, in SNRPE. This expands the mutational and ethnic spectrum of HHS.
“…Exanthems due to viral infections typically present within 14 days of viral symptom onset. 4 Skin rashes in COVID-19 are believed to present around the same time as other symptoms, typically during the first few days of fever and respiratory symptoms. 1 In this cohort, only a minority of exanthems (n = 7/39; 17.9%) developed within 14 days of COVID-19 symptom onset to be considered for a viral rash.…”
“…Shielding behaviour is likely to have contributed to the lower risk of adverse Covid-19 outcomes and is likely to be an important potential mediator in these groups of patients as suggested by the PsoProtect and CORE-UK study groups. 8…”
Section: Outcomes Of Patients With Chronic Plaque Psoriasis and Hidradenitis Suppurativa On Biologic Therapy During The Covid-19 Pandemicmentioning
confidence: 99%
“…Whilst we did not compare outcomes of patients who had psoriasis/ HS on biologics to those on other systemics only, out of 25 (15.2%) psoriasis patients on additional systemic medications, none tested positive for Covid-19 infection. Shielding behaviour is likely to have contributed to the lower risk of adverse Covid-19 outcomes and is likely to be an important potential mediator in these groups of patients as suggested by the PsoProtect and CORE-UK study groups 8.…”
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