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Jonasson, Jenni
Publications (6 of 6) Show all publications
van der Crabben, S. N., Mörner, S., Lundström, A., Jonasson, J., Bikker, H., Amin, A. S., . . . Wilde, A. A. M. (2022). Should variants of unknown significance (VUS) be disclosed to patients in cardiogenetics or not; only in case of high suspicion of pathogenicity?. European Journal of Human Genetics, 30, 1208-1210
Open this publication in new window or tab >>Should variants of unknown significance (VUS) be disclosed to patients in cardiogenetics or not; only in case of high suspicion of pathogenicity?
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2022 (English)In: European Journal of Human Genetics, ISSN 1018-4813, E-ISSN 1476-5438, Vol. 30, p. 1208-1210Article in journal, Editorial material (Refereed) Published
Place, publisher, year, edition, pages
Springer Nature, 2022
National Category
Medical Genetics
Identifiers
urn:nbn:se:umu:diva-199393 (URN)10.1038/s41431-022-01173-z (DOI)000844578000001 ()36008533 (PubMedID)2-s2.0-85137082057 (Scopus ID)
Available from: 2022-09-29 Created: 2022-09-29 Last updated: 2023-05-25Bibliographically approved
Hellman, U., Lång, K., Ihse, E., Jonasson, J., Olsson, M., Lundgren, H.-E., . . . Anan, I. (2019). Transthyretin Glu54Leu - an unknown mutation within the Swedish population associated with amyloid cardiomyopathy and a unique fibril type. Scandinavian Journal of Clinical and Laboratory Investigation, 79(6), 372-376
Open this publication in new window or tab >>Transthyretin Glu54Leu - an unknown mutation within the Swedish population associated with amyloid cardiomyopathy and a unique fibril type
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2019 (English)In: Scandinavian Journal of Clinical and Laboratory Investigation, ISSN 0036-5513, E-ISSN 1502-7686, Vol. 79, no 6, p. 372-376Article in journal (Refereed) Published
Abstract [en]

For the first time, we report of a Swedish family of five individuals with a TTR Glu54Leu (p. Glu74Leu) mutation in the transthyretin gene. This mutation has been previously described a few times in the literature, but no phenotypic or clinical description has been done before. The most common mutation in the Swedish population is TTRVal30Met and is mostly found in the Northern part of Sweden. Interestingly, the TTRGlu54Leu mutation was found in the same endemic area. The main phenotype of the TTR Glu54Leu patients is severe cardiomyopathy, which resulted in heart transplantation for the index person. As previously seen for ATTR amyloidosis patients with mainly cardiomyopathy, the amyloid fibrils consisted of a mixture of full-length and fragmented TTR species. However, western blot analyses detected a previously unrecognized band, indicating that these patients may have a third, so far unrecognized, fibril composition type that is distinct from the usual type A band pattern.

Place, publisher, year, edition, pages
Taylor & Francis, 2019
Keywords
Amyloidosis, amyloid fibril, cardiomyopathy, neuropathy, transthyretin
National Category
Cardiac and Cardiovascular Systems
Identifiers
urn:nbn:se:umu:diva-160383 (URN)10.1080/00365513.2019.1624977 (DOI)000474016000001 ()31169435 (PubMedID)2-s2.0-85067607042 (Scopus ID)
Funder
Knut and Alice Wallenberg FoundationVästerbotten County Council
Available from: 2019-06-18 Created: 2019-06-18 Last updated: 2023-03-23Bibliographically approved
Stattin, E.-L., Westin, I. M., Cederquist, K., Jonasson, J., Jonsson, B.-A., Mörner, S., . . . Wisten, A. (2016). Genetic screening in sudden cardiac death in the young can save future lives. International journal of legal medicine, 130(1), 59-66
Open this publication in new window or tab >>Genetic screening in sudden cardiac death in the young can save future lives
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2016 (English)In: International journal of legal medicine, ISSN 0937-9827, E-ISSN 1437-1596, Vol. 130, no 1, p. 59-66Article in journal (Refereed) Published
Abstract [en]

BACKGROUND: Autopsy of sudden cardiac death (SCD) in the young shows a structurally and histologically normal heart in about one third of cases. Sudden death in these cases is believed to be attributed in a high percentage to inherited arrhythmogenic diseases. The purpose of this study was to investigate the value of performing post-mortem genetic analysis for autopsy-negative sudden unexplained death (SUD) in 1 to 35 year olds.

METHODS AND RESULTS: From January 2009 to December 2011, samples from 15 cases suffering SUD were referred to the Department of Clinical Genetics, Umeå University Hospital, Sweden, for molecular genetic evaluation. PCR and bidirectional Sanger sequencing of genes important for long QT syndrome (LQTS), short QT syndrome (SQTS), Brugada syndrome type 1 (BrS1), and catecholaminergic polymorphic ventricular tachycardia (CPVT) (KCNQ1, KCNH2, SCN5A, KCNE1, KCNE2, and RYR2) was performed. Multiplex ligation-dependent probe amplification (MLPA) was used to detect large deletions or duplications in the LQTS genes. Six pathogenic sequence variants (four LQTS and two CPVT) were discovered in 15 SUD cases (40%). Ten first-degree family members were found to be mutation carriers (seven LQTS and three CPVT).

CONCLUSION: Cardiac ion channel genetic testing in autopsy-negative sudden death victims has a high diagnostic yield, with identification of the disease in 40 of families. First-degree family members should be offered predictive testing, clinical evaluation, and treatment with the ultimate goal to prevent sudden death.

Keywords
Sudden unexplained death, Sudden cardiac death, Molecular autopsy, Long QT syndrome, Catecholaminergic polymorphic ventricular tachycardia
National Category
Medical Genetics
Identifiers
urn:nbn:se:umu:diva-128555 (URN)10.1007/s00414-015-1237-8 (DOI)000368685400006 ()26228265 (PubMedID)2-s2.0-84954360690 (Scopus ID)
Available from: 2016-12-07 Created: 2016-12-07 Last updated: 2024-01-17Bibliographically approved
Olsson, M., Jonasson, J., Cederquist, K. & Suhr, O. B. (2014). Frequency of the transthyretin Val30Met mutation in the northern Swedish population. Amyloid: Journal of Protein Folding Disorders, 21(1), 18-20
Open this publication in new window or tab >>Frequency of the transthyretin Val30Met mutation in the northern Swedish population
2014 (English)In: Amyloid: Journal of Protein Folding Disorders, ISSN 1350-6129, E-ISSN 1744-2818, Vol. 21, no 1, p. 18-20Article in journal (Other academic) Published
Abstract [en]

By genotyping a large number of samples from the Northern Sweden Health and Disease Study cohort, a carrier frequency could be determined for the Skelleftea and Lycksele populations. A previous study of the amyloidogenic transthyretin mutation TTRV30M in Northern Sweden's endemic area has shown a large variation in carrier frequency and penetrance of the trait within the area. However, the estimations have been based on a small sample size within the different regions in the area and therefore, the wide variation in TTRV30M carrier frequency observed between the Lycksele and Skelleftea populations are uncertain. Based on a total of 3460 samples, the estimated overall carrier frequency in the two regions was 1.82% with a carrier frequency in the Skelleftea and Lycksele population of 1.63% and 2.02%, respectively. Thus, the previously reported extremely high frequency in the Lycksele region compared to that of the Skelleftea region could not be substantiated. However, it does not change the previous finding of a surprisingly higher carrier frequency in the population from endemic area of Northern Sweden compared to that reported from endemic areas in Portugal.

Keywords
amyloidosis-hereditary-neuropathic, ATTRV30M (p.ATTRV50M), frequency, genotyping, mutation, transthyretin, TTR c.(Val50Met)
National Category
Medical Genetics
Research subject
Genetics
Identifiers
urn:nbn:se:umu:diva-34124 (URN)10.3109/13506129.2013.860027 (DOI)000335764200003 ()2-s2.0-84896695696 (Scopus ID)
Note

Originally published in dissertation in manuscript form.

Available from: 2010-05-12 Created: 2010-05-12 Last updated: 2023-03-24Bibliographically approved
Stattin, E.-L., Boström, I. M., Winbo, A., Cederquist, K., Jonasson, J., Jonsson, B.-A., . . . Norberg, A. (2012). Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing. BMC Cardiovascular Disorders, 12, 95
Open this publication in new window or tab >>Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing
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2012 (English)In: BMC Cardiovascular Disorders, ISSN 1471-2261, E-ISSN 1471-2261, Vol. 12, p. 95-Article in journal (Refereed) Published
Abstract [en]

Background: Long QT syndrome (LQTS) is an inherited arrhythmic disorder characterised by prolongation of the QT interval on ECG, presence of syncope and sudden death. The symptoms in LQTS patients are highly variable, and genotype influences the clinical course. This study aims to report the spectrum of LQTS mutations in a Swedish cohort.

Methods: Between March 2006 and October 2009, two hundred, unrelated index cases were referred to the Department of Clinical Genetics, Umea University Hospital, Sweden, for LQTS genetic testing. We scanned five of the LQTS-susceptibility genes (KCNQ1, KCNH2, SCN5A, KCNE1, and KCNE2) for mutations by DHPLC and/or sequencing. We applied MLPA to detect large deletions or duplications in the KCNQ1, KCNH2, SCN5A, KCNE1, and KCNE2 genes. Furthermore, the gene RYR2 was screened in 36 selected LQTS genotype-negative patients to detect cases with the clinically overlapping disease catecholaminergic polymorphic ventricular tachycardia (CPVT).

Results: In total, a disease-causing mutation was identified in 103 of the 200 (52%) index cases. Of these, altered exon copy numbers in the KCNH2 gene accounted for 2% of the mutations, whereas a RYR2 mutation accounted for 3% of the mutations. The genotype-positive cases stemmed from 64 distinct mutations, of which 28% were novel to this cohort. The majority of the distinct mutations were found in a single case (80%), whereas 20% of the mutations were observed more than once. Two founder mutations, KCNQ1 p.Y111C and KCNQ1 p.R518*, accounted for 25% of the genotype-positive index cases. Genetic cascade screening of 481 relatives to the 103 index cases with an identified mutation revealed 41% mutation carriers who were at risk of cardiac events such as syncope or sudden unexpected death.

Conclusion: In this cohort of Swedish index cases with suspected LQTS, a disease-causing mutation was identified in 52% of the referred patients. Copy number variations explained 2% of the mutations and 3 of 36 selected cases (8%) harboured a mutation in the RYR2 gene. The mutation panorama is characterised by founder mutations (25%), even so, this cohort increases the amount of known LQTS-associated mutations, as approximately one-third (28%) of the detected mutations were unique.

Place, publisher, year, edition, pages
BioMed Central, 2012
Keywords
Arrhythmia, Long QT syndrome, Ion-channel, Founder mutation, Variant of unknown significance
National Category
Cardiac and Cardiovascular Systems
Identifiers
urn:nbn:se:umu:diva-64060 (URN)10.1186/1471-2261-12-95 (DOI)000312312500001 ()2-s2.0-84867742520 (Scopus ID)
Available from: 2013-01-15 Created: 2013-01-14 Last updated: 2023-03-24Bibliographically approved
Olsson, M., Norgren, N., Obayashi, K., Plante-Bordeneuve, V., Suhr, O. B., Cederquist, K. & Jonasson, J. (2010). A possible role for miRNA silencing in disease phenotype variation in Swedish transthyretin V30M carriers. BMC Medical Genetics, 11, 130
Open this publication in new window or tab >>A possible role for miRNA silencing in disease phenotype variation in Swedish transthyretin V30M carriers
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2010 (English)In: BMC Medical Genetics, E-ISSN 1471-2350, Vol. 11, p. 130-Article in journal (Refereed) Published
Abstract [en]

Our results are the first to show the presence of a 3'UTR polymorphism on the V30M haplotype in Swedish carriers, which can serve as a miRNA binding site potentially leading to down-regulated expression from the mutated TTR allele. This finding may be related to the low penetrance and high age at onset of the disease observed in the Swedish patient population.

Keywords
Allele Frequency; Amyloidosis; Amyloid Neuropathies, Familial; Humans; MicroRNA; Polymorphism, Single Nucleotide; Transthyretin; 3' Untranslated Regions/genetics
National Category
Medical Genetics
Research subject
Genetics
Identifiers
urn:nbn:se:umu:diva-39677 (URN)10.1186/1471-2350-11-130 (DOI)000283195800001 ()20840742 (PubMedID)2-s2.0-77956470387 (Scopus ID)
Available from: 2011-02-03 Created: 2011-02-03 Last updated: 2024-01-17Bibliographically approved
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