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Indirect evaluation of amyloid deposition by ultrasonography and its relationship with MEFV gene mutation in FMF patients
Objective The most significant complication in familial mediterranean fever (FMF) patients is dysfunction and organ failure developing depending on amyloid deposition in organs. The golden standard for showing amyloid deposition is the biopsy; however, tissue stiffness was examined by shear wave ela...
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Published in: | Journal of clinical ultrasound 2023-05, Vol.51 (4), p.715-722 |
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description | Objective
The most significant complication in familial mediterranean fever (FMF) patients is dysfunction and organ failure developing depending on amyloid deposition in organs. The golden standard for showing amyloid deposition is the biopsy; however, tissue stiffness was examined by shear wave elastography as a non‐invasive method in a restricted number of studies conducted, and it is considered that amyloid deposition can be shown indirectly. In our study, we aimed to indirectly evaluate amyloid deposition in organs with Shear wave and Doppler ultrasonography and to reveal its relationship with MEFV gene mutation analysis.
Method
42 FMF patients with normal thyroid and renal function tests and 35 participants with no FMF symptoms were included in our study. FMF patients were grouped depending on their MEFV mutation analyses. Thyroid, salivary glands, and renal parenchymal tissue stiffness were evaluated by shear wave elastography. Thyroidal artery and both renal artery resistances were evaluated by Doppler ultrasonography.
Results
Both parotis gland, thyroid and renal parenchymal stiffness and arterial vascular resistances in the patient group were found higher than the control group. A significant difference was not found in any parameters in classification based on gender. Tissue stiffness and vascular resistance values in the patient group with M694V homozygote mutation were found statistically significantly higher than the other mutation groups (p |
doi_str_mv | 10.1002/jcu.23409 |
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fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2743505806</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2743505806</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3139-85c3025a844322d349f9c6029d6cf8bc290d89cb4b993c827a1d2a042d3305593</originalsourceid><addsrcrecordid>eNp1kU1v1DAQhi0EokvhwB9AlrjAIe34K4mPaNWFVq16ablaju10vUriYCet8u8xm8IBqadXM3rm0UgvQh8JnBEAen4w8xllHOQrtCEgqwJAlq_RJgcpaCXICXqX0gEASiHEW3TCSs4lI2yDlsvB-ujMhN2j7mY9-TDg0GLdL13wFls3huSP22bBczdFncIQHqIe9wvWg8V-Sji67niZ9n7ET37a45uL3U_84AaH-3larX7Au5sdHvPkhim9R29a3SX34TlP0f3u4m77o7i-_X65_XZdmPygLGphGFCha84ZpZZx2UpTApW2NG3dGCrB1tI0vJGSmZpWmliqgWeUgRCSnaIvq3eM4dfs0qR6n4zrOj24MCdFK84EiBrKjH7-Dz2EOQ75O0VrqGouq4pk6utKmRhSiq5VY_S9josioP70oXIf6thHZj89G-emd_Yf-beADJyvwJPv3PKySV1t71flb-T8lDo</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2807849771</pqid></control><display><type>article</type><title>Indirect evaluation of amyloid deposition by ultrasonography and its relationship with MEFV gene mutation in FMF patients</title><source>Wiley-Blackwell Read & Publish Collection</source><creator>Urfali, Mine ; Yilmaz, Gürkan ; Özkul, Bahattin ; Urfali, Furkan Ertürk</creator><creatorcontrib>Urfali, Mine ; Yilmaz, Gürkan ; Özkul, Bahattin ; Urfali, Furkan Ertürk</creatorcontrib><description>Objective
The most significant complication in familial mediterranean fever (FMF) patients is dysfunction and organ failure developing depending on amyloid deposition in organs. The golden standard for showing amyloid deposition is the biopsy; however, tissue stiffness was examined by shear wave elastography as a non‐invasive method in a restricted number of studies conducted, and it is considered that amyloid deposition can be shown indirectly. In our study, we aimed to indirectly evaluate amyloid deposition in organs with Shear wave and Doppler ultrasonography and to reveal its relationship with MEFV gene mutation analysis.
Method
42 FMF patients with normal thyroid and renal function tests and 35 participants with no FMF symptoms were included in our study. FMF patients were grouped depending on their MEFV mutation analyses. Thyroid, salivary glands, and renal parenchymal tissue stiffness were evaluated by shear wave elastography. Thyroidal artery and both renal artery resistances were evaluated by Doppler ultrasonography.
Results
Both parotis gland, thyroid and renal parenchymal stiffness and arterial vascular resistances in the patient group were found higher than the control group. A significant difference was not found in any parameters in classification based on gender. Tissue stiffness and vascular resistance values in the patient group with M694V homozygote mutation were found statistically significantly higher than the other mutation groups (p < 0.001).
Conclusion
Our study shows that identifying genetic mutation type in FMF patients will help determine possibly amyloidosis risk. Imaging of tissue stiffness by shear wave elastography and evaluation of vascular resistance by Doppler can be useful for routine screening of those patients.
Increased AA amyloid in the blood during FMF attacks impairs tissue functions and increases tissue stiffness. Tissue stiffness and increased vascular resistance due to tissue stiffness can be evaluated with ultrasound.</description><identifier>ISSN: 0091-2751</identifier><identifier>EISSN: 1097-0096</identifier><identifier>DOI: 10.1002/jcu.23409</identifier><identifier>PMID: 36449313</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject>ami̇loi̇dosi̇s ; Amyloidosis ; Amyloidosis - complications ; Amyloidosis - diagnostic imaging ; Amyloidosis - genetics ; Biopsy ; Deposition ; Doppler effect ; elastography ; Evaluation ; Familial Mediterranean fever ; Familial Mediterranean Fever - complications ; Familial Mediterranean Fever - diagnostic imaging ; Familial Mediterranean Fever - genetics ; Humans ; MEFV gene ; Mutation ; Organs ; Patients ; Point mutation ; Pyrin - genetics ; Pyrin protein ; Renal artery ; Renal function ; Salivary gland ; Salivary glands ; Shear ; Stiffness ; Thyroid ; Thyroid gland ; Tissues ; Ultrasonic imaging ; Ultrasonography - adverse effects</subject><ispartof>Journal of clinical ultrasound, 2023-05, Vol.51 (4), p.715-722</ispartof><rights>2022 Wiley Periodicals LLC.</rights><rights>2023 Wiley Periodicals LLC.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3139-85c3025a844322d349f9c6029d6cf8bc290d89cb4b993c827a1d2a042d3305593</cites><orcidid>0000-0002-9232-2220 ; 0000-0002-4875-7761 ; 0000-0002-5472-2530 ; 0000-0003-3339-8329</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36449313$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Urfali, Mine</creatorcontrib><creatorcontrib>Yilmaz, Gürkan</creatorcontrib><creatorcontrib>Özkul, Bahattin</creatorcontrib><creatorcontrib>Urfali, Furkan Ertürk</creatorcontrib><title>Indirect evaluation of amyloid deposition by ultrasonography and its relationship with MEFV gene mutation in FMF patients</title><title>Journal of clinical ultrasound</title><addtitle>J Clin Ultrasound</addtitle><description>Objective
The most significant complication in familial mediterranean fever (FMF) patients is dysfunction and organ failure developing depending on amyloid deposition in organs. The golden standard for showing amyloid deposition is the biopsy; however, tissue stiffness was examined by shear wave elastography as a non‐invasive method in a restricted number of studies conducted, and it is considered that amyloid deposition can be shown indirectly. In our study, we aimed to indirectly evaluate amyloid deposition in organs with Shear wave and Doppler ultrasonography and to reveal its relationship with MEFV gene mutation analysis.
Method
42 FMF patients with normal thyroid and renal function tests and 35 participants with no FMF symptoms were included in our study. FMF patients were grouped depending on their MEFV mutation analyses. Thyroid, salivary glands, and renal parenchymal tissue stiffness were evaluated by shear wave elastography. Thyroidal artery and both renal artery resistances were evaluated by Doppler ultrasonography.
Results
Both parotis gland, thyroid and renal parenchymal stiffness and arterial vascular resistances in the patient group were found higher than the control group. A significant difference was not found in any parameters in classification based on gender. Tissue stiffness and vascular resistance values in the patient group with M694V homozygote mutation were found statistically significantly higher than the other mutation groups (p < 0.001).
Conclusion
Our study shows that identifying genetic mutation type in FMF patients will help determine possibly amyloidosis risk. Imaging of tissue stiffness by shear wave elastography and evaluation of vascular resistance by Doppler can be useful for routine screening of those patients.
Increased AA amyloid in the blood during FMF attacks impairs tissue functions and increases tissue stiffness. Tissue stiffness and increased vascular resistance due to tissue stiffness can be evaluated with ultrasound.</description><subject>ami̇loi̇dosi̇s</subject><subject>Amyloidosis</subject><subject>Amyloidosis - complications</subject><subject>Amyloidosis - diagnostic imaging</subject><subject>Amyloidosis - genetics</subject><subject>Biopsy</subject><subject>Deposition</subject><subject>Doppler effect</subject><subject>elastography</subject><subject>Evaluation</subject><subject>Familial Mediterranean fever</subject><subject>Familial Mediterranean Fever - complications</subject><subject>Familial Mediterranean Fever - diagnostic imaging</subject><subject>Familial Mediterranean Fever - genetics</subject><subject>Humans</subject><subject>MEFV gene</subject><subject>Mutation</subject><subject>Organs</subject><subject>Patients</subject><subject>Point mutation</subject><subject>Pyrin - genetics</subject><subject>Pyrin protein</subject><subject>Renal artery</subject><subject>Renal function</subject><subject>Salivary gland</subject><subject>Salivary glands</subject><subject>Shear</subject><subject>Stiffness</subject><subject>Thyroid</subject><subject>Thyroid gland</subject><subject>Tissues</subject><subject>Ultrasonic imaging</subject><subject>Ultrasonography - adverse effects</subject><issn>0091-2751</issn><issn>1097-0096</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp1kU1v1DAQhi0EokvhwB9AlrjAIe34K4mPaNWFVq16ablaju10vUriYCet8u8xm8IBqadXM3rm0UgvQh8JnBEAen4w8xllHOQrtCEgqwJAlq_RJgcpaCXICXqX0gEASiHEW3TCSs4lI2yDlsvB-ujMhN2j7mY9-TDg0GLdL13wFls3huSP22bBczdFncIQHqIe9wvWg8V-Sji67niZ9n7ET37a45uL3U_84AaH-3larX7Au5sdHvPkhim9R29a3SX34TlP0f3u4m77o7i-_X65_XZdmPygLGphGFCha84ZpZZx2UpTApW2NG3dGCrB1tI0vJGSmZpWmliqgWeUgRCSnaIvq3eM4dfs0qR6n4zrOj24MCdFK84EiBrKjH7-Dz2EOQ75O0VrqGouq4pk6utKmRhSiq5VY_S9josioP70oXIf6thHZj89G-emd_Yf-beADJyvwJPv3PKySV1t71flb-T8lDo</recordid><startdate>202305</startdate><enddate>202305</enddate><creator>Urfali, Mine</creator><creator>Yilmaz, Gürkan</creator><creator>Özkul, Bahattin</creator><creator>Urfali, Furkan Ertürk</creator><general>John Wiley & Sons, Inc</general><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>M7Z</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-9232-2220</orcidid><orcidid>https://orcid.org/0000-0002-4875-7761</orcidid><orcidid>https://orcid.org/0000-0002-5472-2530</orcidid><orcidid>https://orcid.org/0000-0003-3339-8329</orcidid></search><sort><creationdate>202305</creationdate><title>Indirect evaluation of amyloid deposition by ultrasonography and its relationship with MEFV gene mutation in FMF patients</title><author>Urfali, Mine ; Yilmaz, Gürkan ; Özkul, Bahattin ; Urfali, Furkan Ertürk</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3139-85c3025a844322d349f9c6029d6cf8bc290d89cb4b993c827a1d2a042d3305593</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>ami̇loi̇dosi̇s</topic><topic>Amyloidosis</topic><topic>Amyloidosis - complications</topic><topic>Amyloidosis - diagnostic imaging</topic><topic>Amyloidosis - genetics</topic><topic>Biopsy</topic><topic>Deposition</topic><topic>Doppler effect</topic><topic>elastography</topic><topic>Evaluation</topic><topic>Familial Mediterranean fever</topic><topic>Familial Mediterranean Fever - complications</topic><topic>Familial Mediterranean Fever - diagnostic imaging</topic><topic>Familial Mediterranean Fever - genetics</topic><topic>Humans</topic><topic>MEFV gene</topic><topic>Mutation</topic><topic>Organs</topic><topic>Patients</topic><topic>Point mutation</topic><topic>Pyrin - genetics</topic><topic>Pyrin protein</topic><topic>Renal artery</topic><topic>Renal function</topic><topic>Salivary gland</topic><topic>Salivary glands</topic><topic>Shear</topic><topic>Stiffness</topic><topic>Thyroid</topic><topic>Thyroid gland</topic><topic>Tissues</topic><topic>Ultrasonic imaging</topic><topic>Ultrasonography - adverse effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Urfali, Mine</creatorcontrib><creatorcontrib>Yilmaz, Gürkan</creatorcontrib><creatorcontrib>Özkul, Bahattin</creatorcontrib><creatorcontrib>Urfali, Furkan Ertürk</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of clinical ultrasound</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Urfali, Mine</au><au>Yilmaz, Gürkan</au><au>Özkul, Bahattin</au><au>Urfali, Furkan Ertürk</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Indirect evaluation of amyloid deposition by ultrasonography and its relationship with MEFV gene mutation in FMF patients</atitle><jtitle>Journal of clinical ultrasound</jtitle><addtitle>J Clin Ultrasound</addtitle><date>2023-05</date><risdate>2023</risdate><volume>51</volume><issue>4</issue><spage>715</spage><epage>722</epage><pages>715-722</pages><issn>0091-2751</issn><eissn>1097-0096</eissn><abstract>Objective
The most significant complication in familial mediterranean fever (FMF) patients is dysfunction and organ failure developing depending on amyloid deposition in organs. The golden standard for showing amyloid deposition is the biopsy; however, tissue stiffness was examined by shear wave elastography as a non‐invasive method in a restricted number of studies conducted, and it is considered that amyloid deposition can be shown indirectly. In our study, we aimed to indirectly evaluate amyloid deposition in organs with Shear wave and Doppler ultrasonography and to reveal its relationship with MEFV gene mutation analysis.
Method
42 FMF patients with normal thyroid and renal function tests and 35 participants with no FMF symptoms were included in our study. FMF patients were grouped depending on their MEFV mutation analyses. Thyroid, salivary glands, and renal parenchymal tissue stiffness were evaluated by shear wave elastography. Thyroidal artery and both renal artery resistances were evaluated by Doppler ultrasonography.
Results
Both parotis gland, thyroid and renal parenchymal stiffness and arterial vascular resistances in the patient group were found higher than the control group. A significant difference was not found in any parameters in classification based on gender. Tissue stiffness and vascular resistance values in the patient group with M694V homozygote mutation were found statistically significantly higher than the other mutation groups (p < 0.001).
Conclusion
Our study shows that identifying genetic mutation type in FMF patients will help determine possibly amyloidosis risk. Imaging of tissue stiffness by shear wave elastography and evaluation of vascular resistance by Doppler can be useful for routine screening of those patients.
Increased AA amyloid in the blood during FMF attacks impairs tissue functions and increases tissue stiffness. Tissue stiffness and increased vascular resistance due to tissue stiffness can be evaluated with ultrasound.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>36449313</pmid><doi>10.1002/jcu.23409</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-9232-2220</orcidid><orcidid>https://orcid.org/0000-0002-4875-7761</orcidid><orcidid>https://orcid.org/0000-0002-5472-2530</orcidid><orcidid>https://orcid.org/0000-0003-3339-8329</orcidid></addata></record> |
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subjects | ami̇loi̇dosi̇s Amyloidosis Amyloidosis - complications Amyloidosis - diagnostic imaging Amyloidosis - genetics Biopsy Deposition Doppler effect elastography Evaluation Familial Mediterranean fever Familial Mediterranean Fever - complications Familial Mediterranean Fever - diagnostic imaging Familial Mediterranean Fever - genetics Humans MEFV gene Mutation Organs Patients Point mutation Pyrin - genetics Pyrin protein Renal artery Renal function Salivary gland Salivary glands Shear Stiffness Thyroid Thyroid gland Tissues Ultrasonic imaging Ultrasonography - adverse effects |
title | Indirect evaluation of amyloid deposition by ultrasonography and its relationship with MEFV gene mutation in FMF patients |
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