Maternal Serum Amyloid a Level as a Novel Marker of Primary Unexplained Recurrent Early Pregnancy Loss

Background: Recurrent abortion affects 1-2% of women. Serum Amyloid A belongs to a family of apolipoproteins produced in response to cytokines released by activated monocytes and macrophages, isolated in the last 50 years. Our current study emphasizes human SAA protein as a sensitive biochemical mar...

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Veröffentlicht in:Journal of pioneering medical sciences 2024-04, Vol.13 (2), p.182-186
Hauptverfasser: Mohmmed, Maha Jawad, Jasim, Halah Razzaq, AL-Turiahi, Azhar Mousa
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container_end_page 186
container_issue 2
container_start_page 182
container_title Journal of pioneering medical sciences
container_volume 13
creator Mohmmed, Maha Jawad
Jasim, Halah Razzaq
AL-Turiahi, Azhar Mousa
description Background: Recurrent abortion affects 1-2% of women. Serum Amyloid A belongs to a family of apolipoproteins produced in response to cytokines released by activated monocytes and macrophages, isolated in the last 50 years. Our current study emphasizes human SAA protein as a sensitive biochemical marker for primary unexplained recurrent miscarriage. The aim of the current study is to examine the hypothesis that primary unexplained REPL might be associated with high maternal serum levels of SAA, which in turn could lead to defective trophoblastic invasion into the decidua, and subsequent pregnancy failure and miscarriage. Patients and Method: A prospective study (case control study) in Al-Zahraa Maternity Hospital, Najaf, Iraq, from first of January to the first of December of 2019. The study was conducted among 91 who were divided into two groups Group 1: women with missed miscarriage in the first trimester with at least two consecutive primary unexplained REPLs and no previous live births were enrolled. Group 2: A control group was formed of women with miscarriage no history of REPL who had at least one previous uneventful pregnancy with no adverse outcomes. Serum samples were collected to measure SAA levels. Result: The main outcome was the association between SAA and primary unexplained REPL. A total number of 91 participants. Mean SAA level was significantly higher among women with REPL than among women in the control group (P
doi_str_mv 10.61091/jpms202413227
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Serum Amyloid A belongs to a family of apolipoproteins produced in response to cytokines released by activated monocytes and macrophages, isolated in the last 50 years. Our current study emphasizes human SAA protein as a sensitive biochemical marker for primary unexplained recurrent miscarriage. The aim of the current study is to examine the hypothesis that primary unexplained REPL might be associated with high maternal serum levels of SAA, which in turn could lead to defective trophoblastic invasion into the decidua, and subsequent pregnancy failure and miscarriage. Patients and Method: A prospective study (case control study) in Al-Zahraa Maternity Hospital, Najaf, Iraq, from first of January to the first of December of 2019. The study was conducted among 91 who were divided into two groups Group 1: women with missed miscarriage in the first trimester with at least two consecutive primary unexplained REPLs and no previous live births were enrolled. Group 2: A control group was formed of women with miscarriage no history of REPL who had at least one previous uneventful pregnancy with no adverse outcomes. Serum samples were collected to measure SAA levels. Result: The main outcome was the association between SAA and primary unexplained REPL. A total number of 91 participants. Mean SAA level was significantly higher among women with REPL than among women in the control group (P&lt;0.001). The SAA level was dependent indicator of primary unexplained REPL, P&lt;0.001 Elevated SAA levels found among women with primary unexplained REPL could represent biomarker for this complication of pregnancy. Conclusions: The present findings suggest that SAA is potentially a novel marker for primary unexplained REPL that warrants further investigation. For example, studies could be conducted to compare SAA levels among women with a history of primary unexplained REPL during the pregnant and non-pregnant states, as well as before and after miscarriage. In future, such studies might guide the timing for initiation of new treatments, such as gene therapy or the use of immune-receptor antagonists.</description><identifier>ISSN: 2309-7981</identifier><identifier>EISSN: 2309-7981</identifier><identifier>DOI: 10.61091/jpms202413227</identifier><language>eng</language><ispartof>Journal of pioneering medical sciences, 2024-04, Vol.13 (2), p.182-186</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Mohmmed, Maha Jawad</creatorcontrib><creatorcontrib>Jasim, Halah Razzaq</creatorcontrib><creatorcontrib>AL-Turiahi, Azhar Mousa</creatorcontrib><creatorcontrib>Department of Gynecology &amp; Obstructive, Faculty of Medicine, University of Kufa, Iraq</creatorcontrib><title>Maternal Serum Amyloid a Level as a Novel Marker of Primary Unexplained Recurrent Early Pregnancy Loss</title><title>Journal of pioneering medical sciences</title><description>Background: Recurrent abortion affects 1-2% of women. Serum Amyloid A belongs to a family of apolipoproteins produced in response to cytokines released by activated monocytes and macrophages, isolated in the last 50 years. Our current study emphasizes human SAA protein as a sensitive biochemical marker for primary unexplained recurrent miscarriage. The aim of the current study is to examine the hypothesis that primary unexplained REPL might be associated with high maternal serum levels of SAA, which in turn could lead to defective trophoblastic invasion into the decidua, and subsequent pregnancy failure and miscarriage. Patients and Method: A prospective study (case control study) in Al-Zahraa Maternity Hospital, Najaf, Iraq, from first of January to the first of December of 2019. The study was conducted among 91 who were divided into two groups Group 1: women with missed miscarriage in the first trimester with at least two consecutive primary unexplained REPLs and no previous live births were enrolled. Group 2: A control group was formed of women with miscarriage no history of REPL who had at least one previous uneventful pregnancy with no adverse outcomes. Serum samples were collected to measure SAA levels. Result: The main outcome was the association between SAA and primary unexplained REPL. A total number of 91 participants. Mean SAA level was significantly higher among women with REPL than among women in the control group (P&lt;0.001). The SAA level was dependent indicator of primary unexplained REPL, P&lt;0.001 Elevated SAA levels found among women with primary unexplained REPL could represent biomarker for this complication of pregnancy. Conclusions: The present findings suggest that SAA is potentially a novel marker for primary unexplained REPL that warrants further investigation. For example, studies could be conducted to compare SAA levels among women with a history of primary unexplained REPL during the pregnant and non-pregnant states, as well as before and after miscarriage. In future, such studies might guide the timing for initiation of new treatments, such as gene therapy or the use of immune-receptor antagonists.</description><issn>2309-7981</issn><issn>2309-7981</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNpVkMtOwzAURC0EElXplrV_IOX6kcReVlV5SCkgKOvo1rlGLXlUdorI37dQFrCasxjNjIaxawHTTIAVN9tdEyVILZSU-RkbSQU2ya0R53_4kk1i3AKAUFoKMCPml9hTaLHmrxT2DZ81Q91tKo68oE-qOcYjPnbfuMTwQYF3nj-HTYNh4G8tfe1q3LRU8Rdy-xCo7fkCQz0cPfTeYusGXnQxXrELj3Wkya-O2ep2sZrfJ8XT3cN8ViROZLpP1sahM2ptUocIVeaETp0xWntpJGQVVTo1CpTNvHaAMl_nqbU2J2-dk1KN2fQU68KxNJAvd6eppYDy56fy30_qACAyXB4</recordid><startdate>20240429</startdate><enddate>20240429</enddate><creator>Mohmmed, Maha Jawad</creator><creator>Jasim, Halah Razzaq</creator><creator>AL-Turiahi, Azhar Mousa</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20240429</creationdate><title>Maternal Serum Amyloid a Level as a Novel Marker of Primary Unexplained Recurrent Early Pregnancy Loss</title><author>Mohmmed, Maha Jawad ; Jasim, Halah Razzaq ; AL-Turiahi, Azhar Mousa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c164t-b8cac83b85caa0d6c145c8844f28206ded45830396f4c0a27b759997ef9cc223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mohmmed, Maha Jawad</creatorcontrib><creatorcontrib>Jasim, Halah Razzaq</creatorcontrib><creatorcontrib>AL-Turiahi, Azhar Mousa</creatorcontrib><creatorcontrib>Department of Gynecology &amp; Obstructive, Faculty of Medicine, University of Kufa, Iraq</creatorcontrib><collection>CrossRef</collection><jtitle>Journal of pioneering medical sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mohmmed, Maha Jawad</au><au>Jasim, Halah Razzaq</au><au>AL-Turiahi, Azhar Mousa</au><aucorp>Department of Gynecology &amp; Obstructive, Faculty of Medicine, University of Kufa, Iraq</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Maternal Serum Amyloid a Level as a Novel Marker of Primary Unexplained Recurrent Early Pregnancy Loss</atitle><jtitle>Journal of pioneering medical sciences</jtitle><date>2024-04-29</date><risdate>2024</risdate><volume>13</volume><issue>2</issue><spage>182</spage><epage>186</epage><pages>182-186</pages><issn>2309-7981</issn><eissn>2309-7981</eissn><abstract>Background: Recurrent abortion affects 1-2% of women. Serum Amyloid A belongs to a family of apolipoproteins produced in response to cytokines released by activated monocytes and macrophages, isolated in the last 50 years. Our current study emphasizes human SAA protein as a sensitive biochemical marker for primary unexplained recurrent miscarriage. The aim of the current study is to examine the hypothesis that primary unexplained REPL might be associated with high maternal serum levels of SAA, which in turn could lead to defective trophoblastic invasion into the decidua, and subsequent pregnancy failure and miscarriage. Patients and Method: A prospective study (case control study) in Al-Zahraa Maternity Hospital, Najaf, Iraq, from first of January to the first of December of 2019. The study was conducted among 91 who were divided into two groups Group 1: women with missed miscarriage in the first trimester with at least two consecutive primary unexplained REPLs and no previous live births were enrolled. Group 2: A control group was formed of women with miscarriage no history of REPL who had at least one previous uneventful pregnancy with no adverse outcomes. Serum samples were collected to measure SAA levels. Result: The main outcome was the association between SAA and primary unexplained REPL. A total number of 91 participants. Mean SAA level was significantly higher among women with REPL than among women in the control group (P&lt;0.001). The SAA level was dependent indicator of primary unexplained REPL, P&lt;0.001 Elevated SAA levels found among women with primary unexplained REPL could represent biomarker for this complication of pregnancy. Conclusions: The present findings suggest that SAA is potentially a novel marker for primary unexplained REPL that warrants further investigation. For example, studies could be conducted to compare SAA levels among women with a history of primary unexplained REPL during the pregnant and non-pregnant states, as well as before and after miscarriage. In future, such studies might guide the timing for initiation of new treatments, such as gene therapy or the use of immune-receptor antagonists.</abstract><doi>10.61091/jpms202413227</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record>
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