Literature DB >> 23196800

Canine serum amyloid A (SAA) measured by automated latex agglutination turbidimetry is useful for routine sensitive and specific detection of systemic inflammation in a general clinical setting.

Michelle B Christensen1, Rebecca Langhorn, Amelia Goddard, Eva B Andreasen, Elena Moldal, Asta Tvarijonaviciute, Jolle Kirpenteijn, Sabrina Jakobsen, Frida Persson, Mads Kjelgaard-Hansen.   

Abstract

Canine serum amyloid A (SAA) is a useful diagnostic marker of systemic inflammation. A latex agglutination turbidimetric immunoassay (LAT) was validated for automated measurements. The aim of the study was to evaluate the clinical applicability of SAA measured by the LAT. SAA was measured in 7 groups of dogs with and without systemic inflammation (n=247). Overlap performance was investigated. Diagnostic performance was compared to body temperature and leukocyte markers. Clinical decision limits for SAA were estimated. In dogs with neurological, neoplastic or gastrointestinal disorders (n=143), it was investigated whether a higher proportion of SAA positive dogs could be detected in cases of complications with risk of systemic inflammation. Significantly higher concentrations of SAA were measured in dogs with (range [48.75; 5,032 mg/l]), compared to dogs without systemic inflammation [0; 56.4 mg/l]. SAA was a more sensitive and specific marker of systemic inflammation (area under the receiver-operating characteristic curve (AUC) 1.00), compared to body temperature (0.6) and segmented neutrophils (best performing leukocyte marker, 0.84). A clinical decision limit of 56.4 mg/l was established giving close to perfect discrimination between dogs with and without systemic inflammation. Higher proportions of SAA-positive dogs were observed in dogs with neurological, neoplastic and gastrointestinal disorders with complications known to increase risk of systemic inflammation, compared to uncomplicated cases. The automated LAT makes SAA applicable as a relevant diagnostic marker of systemic inflammation in dogs for routine random-access real-time use in a general clinical setting.

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Year:  2012        PMID: 23196800     DOI: 10.1292/jvms.12-0404

Source DB:  PubMed          Journal:  J Vet Med Sci        ISSN: 0916-7250            Impact factor:   1.267


  5 in total

1.  Comparison of serum amyloid A and C-reactive protein as diagnostic markers of systemic inflammation in dogs.

Authors:  Michelle B Christensen; Rebecca Langhorn; Amelia Goddard; Eva B Andreasen; Elena Moldal; Asta Tvarijonaviciute; Jolle Kirpensteijn; Sabrina Jakobsen; Frida Persson; Mads Kjelgaard-Hansen
Journal:  Can Vet J       Date:  2014-02       Impact factor: 1.008

2.  Alterations in serum protein electrophoresis profiles during the acute phase response in dogs with acute pancreatitis.

Authors:  Ji-Seon Yoon; Suhee Kim; Jin-Hee Kang; Jinho Park; DoHyeon Yu
Journal:  Can J Vet Res       Date:  2020-01       Impact factor: 1.310

3.  Increased concentrations of Serum amyloid A in dogs with sepsis caused by pyometra.

Authors:  Supranee Jitpean; Ann Pettersson; Odd V Höglund; Bodil Ström Holst; Ulf Olsson; Ragnvi Hagman
Journal:  BMC Vet Res       Date:  2014-11-28       Impact factor: 2.741

4.  Decreased plasma Chromogranin A361-372 (Catestatin) but not Chromogranin A17-38 (Vasostatin) in female dogs with bacterial uterine infection (pyometra).

Authors:  Supranee Jitpean; Mats Stridsberg; Ann Pettersson; Odd V Höglund; Bodil Ström Holst; Ragnvi Hagman
Journal:  BMC Vet Res       Date:  2015-01-31       Impact factor: 2.741

5.  Usefulness of C-reactive protein and serum amyloid A in early detection of postoperative infectious complications to tibial plateau leveling osteotomy in dogs.

Authors:  Karin Löfqvist; Mads Kjelgaard-Hansen; Michelle Brønniche Møller Nielsen
Journal:  Acta Vet Scand       Date:  2018-05-21       Impact factor: 1.695

  5 in total

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