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Amyloid fibrils with fragmented ATTR may be the rule in non-Val30Met ATTR amyloidosis

Ihse, Elisabet, 1977- (author)
Uppsala universitet,Molekylär och morfologisk patologi,Per Westermark
Rapezzi, Claudio (author)
Cardiovascular Dept, University of Bologna, Italy
Merlini, Giampaolo (author)
Amyloid Research and Treatment Center, Scientific Institute Policlinico San Matteo, University of Pavia, Italy
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Benson, Merrill D (author)
Dept of Pathology and Laboratory Medicine, Indiana University School of Medicine and Roudebush VA medical Center, Indianapolis, IN, USA
Ando, Yukio (author)
Dept of Diagnostic Medicine, Graduate School of Medical Sciences, Kumamoto University, Japan
Suhr, Ole B (author)
Dept of Public Health and Clinical Medicine, Umeå University
Leone, Ornella (author)
Pathology Department, S.Orsola-Malpighi Hospital, Bologna, Italy
Lorenzini, Massimiliano (author)
Cardiovascular Dept, University of Bologna, Italy
Quarta, Candida Cristina (author)
Cardiovascular Dept, University of Bologna, Italy
Obici, Laura (author)
Amyloid Research and Treatment Center, Scientific Institute Policlinico San Matteo, University of Pavia, Italy
Lavatelli, Francesca (author)
Amyloid Research and Treatment Center, Scientific Institute Policlinico San Matteo, University of Pavia, Italy
Liepnieks, Juris (author)
Dept of Pathology and Laboratory Medicine, Indiana University School of Medicine and Roudebush VA medical Center, Indianapolis, IN, USA
Ohshima, Toshinori (author)
Dept of Neurology, Graduate School of Medical Sciences, Kumamoto University, Japan
Jono, Hirofumi (author)
Dept of Diagnostic Medicine, Graduate School of Medical Sciences, Kumamoto University, Japan
Westermark, Per (author)
Uppsala universitet,Molekylär och morfologisk patologi
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 (creator_code:org_t)
English.
  • Other publication (other academic/artistic)
Abstract Subject headings
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  • The clinical phenotype of familial ATTR amyloidosis depends to some extent on the particular mutation, but differences exist also within mutations. We have previously described that two types of amyloid fibril compositions exist among Swedish ATTRV30M amyloidosis patients, one consisting of a mixture of intact and fragmented ATTR (type A) and one composed of only intact ATTR (type B). Patients with type A fibrils have a late age of onset and signs of cardiomyopathy, while patients with type B fibrils have an early onset and much less myocardial involvement. The present study aimed to determine if the correlation between fibril type and clinical phenotype is true for familial amyloidosis in general. Cardiac and/or adipose tissue from 48 patients carrying 21 different non-TTRV30M mutations were examined, as well as 7 non-Swedish ATTRV30M patients. Fibril type was determined with western blotting and compared to the patients´ age of onset and degree of cardiomyopathy. Non-Swedish V30M patients showed the same correlation as described for Swedish V30M patients, with fibrils of only full-length ATTR (type B) linked to less myocardial involvement. In contrast, all patients with non-V30M mutations had a fibril composition with ATTR fragments (type A). Some of these patients had onset of disease at young age. The vast majority had increased thickness of left cardiac ventricle, but a few individuals had values within normal limits. This study shows that a fibril composition with fragmented ATTR is very common in ATTR amyloidosis. It also suggests that fibrils composed of only full-length ATTR is an exception, perhaps only found among young ATTRV30M amyloidosis patients.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Andra medicinska och farmaceutiska grundvetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Other Basic Medicine (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Klinisk laboratoriemedicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Clinical Laboratory Medicine (hsv//eng)
NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

Keyword

amyloid
transthyretin
familial amyloidotic polyneuropathy
non-TTRV30M
TTRV30M
cardiomyopathy
fibril composition
Biochemistry
Biokemi
Biology with specialization in Molecular Biology
Biologi med inriktning mot molekylärbiologi
Biomedicinsk laboratorievetenskap
Biomedical Laboratory Science
Experimentell patologi
Experimental Pathology
Medical Biochemistry
Medicinsk biokemi
Molecular Biology
Molekylärbiologi
Pathology
Patologi

Publication and Content Type

vet (subject category)
ovr (subject category)

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