First data on the biological variation and quality specifications for plasma ammonia concentrations in healthy subjects
Most of the factors causing preanalytical and analytical variation in ammonia measurement have been identified. Biological variation data for ammonia is still lacking. We therefore estimated the components of biological variation (within-subject=CVI and between-subject=CVG), reference change value (...
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Published in | Clinical chemistry and laboratory medicine Vol. 54; no. 5; pp. 857 - 863 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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Germany
De Gruyter
01.05.2016
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ISSN | 1434-6621 1437-4331 |
DOI | 10.1515/cclm-2015-0591 |
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Abstract | Most of the factors causing preanalytical and analytical variation in ammonia measurement have been identified. Biological variation data for ammonia is still lacking. We therefore estimated the components of biological variation (within-subject=CVI and between-subject=CVG), reference change value (RCV) and quality specifications for ammonia in a group of healthy individuals using fresh and frozen plasma samples.
Blood samples from 20 healthy subjects were collected in K2EDTA tubes daily over a period of 4 consecutive days from each subject. Each plasma sample was split into two aliquots; one was immediately analyzed as the samples were collected and the other was stored -80 °C until testing at the end of the collection period and analyzed at once in one analytical run. All samples were analyzed in duplicate. Estimations were calculated according to Fraser and Harris methods.
CVI value for fresh samples (13.78%) was significantly lower than that in frozen samples (18.91%) (p<0.001). However, there was no statistically significant difference in CVG values between fresh (16.91%) and frozen (18.43%) samples (p=0.570). The index of individuality did not exceed 1.4 for fresh and frozen samples. The estimated RCVs were high for both fresh and frozen samples (43.37% and 56.85%, respectively). Quality specifications were established.
The present study for the first time described the components of biological variation for ammonia in healthy individuals. These data regarding biological variation of ammonia could be useful for a better evaluation of ammonia test results in clinical interpretation and for determining quality specifications based on biological variation. |
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AbstractList | BACKGROUNDMost of the factors causing preanalytical and analytical variation in ammonia measurement have been identified. Biological variation data for ammonia is still lacking. We therefore estimated the components of biological variation (within-subject=CVI and between-subject=CVG), reference change value (RCV) and quality specifications for ammonia in a group of healthy individuals using fresh and frozen plasma samples.METHODSBlood samples from 20 healthy subjects were collected in K2EDTA tubes daily over a period of 4 consecutive days from each subject. Each plasma sample was split into two aliquots; one was immediately analyzed as the samples were collected and the other was stored -80 °C until testing at the end of the collection period and analyzed at once in one analytical run. All samples were analyzed in duplicate. Estimations were calculated according to Fraser and Harris methods.RESULTSCVI value for fresh samples (13.78%) was significantly lower than that in frozen samples (18.91%) (p<0.001). However, there was no statistically significant difference in CVG values between fresh (16.91%) and frozen (18.43%) samples (p=0.570). The index of individuality did not exceed 1.4 for fresh and frozen samples. The estimated RCVs were high for both fresh and frozen samples (43.37% and 56.85%, respectively). Quality specifications were established.CONCLUSIONSThe present study for the first time described the components of biological variation for ammonia in healthy individuals. These data regarding biological variation of ammonia could be useful for a better evaluation of ammonia test results in clinical interpretation and for determining quality specifications based on biological variation. Most of the factors causing preanalytical and analytical variation in ammonia measurement have been identified. Biological variation data for ammonia is still lacking. We therefore estimated the components of biological variation (within-subject=CVI and between-subject=CVG), reference change value (RCV) and quality specifications for ammonia in a group of healthy individuals using fresh and frozen plasma samples. Blood samples from 20 healthy subjects were collected in K2EDTA tubes daily over a period of 4 consecutive days from each subject. Each plasma sample was split into two aliquots; one was immediately analyzed as the samples were collected and the other was stored -80 °C until testing at the end of the collection period and analyzed at once in one analytical run. All samples were analyzed in duplicate. Estimations were calculated according to Fraser and Harris methods. CVI value for fresh samples (13.78%) was significantly lower than that in frozen samples (18.91%) (p<0.001). However, there was no statistically significant difference in CVG values between fresh (16.91%) and frozen (18.43%) samples (p=0.570). The index of individuality did not exceed 1.4 for fresh and frozen samples. The estimated RCVs were high for both fresh and frozen samples (43.37% and 56.85%, respectively). Quality specifications were established. The present study for the first time described the components of biological variation for ammonia in healthy individuals. These data regarding biological variation of ammonia could be useful for a better evaluation of ammonia test results in clinical interpretation and for determining quality specifications based on biological variation. |
Author | Ozdemir, Seyda Ozcan, Nurgul Ucar, Fatma Ozturk, Alpaslan Erden, Gonul Bulut, Erdem |
Author_xml | – sequence: 1 givenname: Fatma surname: Ucar fullname: Ucar, Fatma email: drfucar@gmail.com organization: Department of Clinical Biochemistry, Diskapi Yildirim Beyazit Training and Research Hospital, Ankara, Turkey – sequence: 2 givenname: Gonul surname: Erden fullname: Erden, Gonul organization: Hacettepe University Medical Faculty, Department of Biochemistry, Ankara, Turkey – sequence: 3 givenname: Seyda surname: Ozdemir fullname: Ozdemir, Seyda organization: Department of Clinical Biochemistry, Diskapi Yildirim Beyazit Training and Research Hospital, Ankara, Turkey – sequence: 4 givenname: Nurgul surname: Ozcan fullname: Ozcan, Nurgul organization: Department of Clinical Biochemistry, Diskapi Yildirim Beyazit Training and Research Hospital, Ankara, Turkey – sequence: 5 givenname: Erdem surname: Bulut fullname: Bulut, Erdem organization: Department of Clinical Biochemistry, Diskapi Yildirim Beyazit Training and Research Hospital, Ankara, Turkey – sequence: 6 givenname: Alpaslan surname: Ozturk fullname: Ozturk, Alpaslan organization: Department of Clinical Biochemistry, Diskapi Yildirim Beyazit Training and Research Hospital, Ankara, Turkey |
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Cites_doi | 10.1067/mpd.2001.111832 10.1016/j.pneurobio.2010.01.012 10.1093/clinchem/46.12.2027 10.1177/000456328802500603 10.1258/000456307780945633 10.1080/08035250500349413 10.1080/00365510410004885 10.1016/j.clinbiochem.2014.05.068 10.1016/S0002-9343(02)01477-8 10.1016/j.clinbiochem.2014.08.013 10.3109/10408368909106595 10.1185/03007995.2012.694362 10.1515/cclm-2012-0701 10.1093/clinchem/30.6.906 10.1136/jclinpath-2014-202693 10.1097/00005792-200205000-00007 10.1007/s00467-011-1838-5 10.1080/10428190701509822 |
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SubjectTerms | Adult ammonia Ammonia - blood between-subject biological variation Female Healthy Volunteers Humans Male Middle Aged reference change value within-subject biological variation Young Adult |
Title | First data on the biological variation and quality specifications for plasma ammonia concentrations in healthy subjects |
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