Calibration of the Periotron 8000® and 6000® by polynomial regression

This paper reports the detailed calibration of the new Periotron 8000® with different fluids and uses the method of least squares to derive polynomial regression equations up to the 6th order, to investigate the most accurate descriptor of the resulting calibration lines. The use of a 4th order poly...

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Vydané v:Journal of periodontal research Ročník 34; číslo 2; s. 79 - 86
Hlavní autori: Chapple, I. L. C., Landini, G., Griffiths, G. S., Patel, N. C., Ward, R. S. N.
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: Oxford, UK Blackwell Publishing Ltd 01.02.1999
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ISSN:0022-3484, 1600-0765
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Abstract This paper reports the detailed calibration of the new Periotron 8000® with different fluids and uses the method of least squares to derive polynomial regression equations up to the 6th order, to investigate the most accurate descriptor of the resulting calibration lines. The use of a 4th order polynomial regression equation (recommended by the manufacturer) provided better coefficients of determination (R2: 0.999) and root mean square errors (RMSE = 1.6) than either linear regression (R2: 0.986, RMSE = 10.9) or quadratic models (R2: 0.998, RMSE = 3.2). Data derived using the manufacturer's MLCONVERT software program lacked accuracy and incurred large errors for volumes > 0.5 μl. Calibrations performed on one day could be used with accuracy to derive volumes >0.1 μl collected on subsequent days, when using the same machine (s.d. for residuals plot=2.49 Periotron units), but this was not the case for different machines (s.d. = 9.57 Periotron units). Varying serum protein concentration by up to 500% had a negligible effect on calculated volumes above 0.1 μl. We conclude that the Periotron 8000® is at least as reliable a machine as the Periotron 6000®, and that the calibration lines for both machines are best described using 4th order polynomial regression equations and “look‐up” tables, rather than quadratic (Periotron 6000®) or the manufacturer's software (Periotron 8000®). Serum seems to be an acceptable GCF substitute for calibrations, which can be performed 1 day, and used on subsequent days for a given machine and for volumes above 0.1 μl.
AbstractList This paper reports the detailed calibration of the new Periotron 8000 with different fluids and uses the method of least squares to derive polynomial regression equations up to the 6th order, to investigate the most accurate descriptor of the resulting calibration lines. The use of a 4th order polynomial regression equation (recommended by the manufacturer) provided better coefficients of determination (R2: 0.999) and root mean square errors (RMSE = 1.6) than either linear regression (R2: 0.986, RMSE = 10.9) or quadratic models (R2: 0.998, RMSE = 3.2). Data derived using the manufacturer's MLCONVERT software program lacked accuracy and incurred large errors for volumes > 0.5 microliter. Calibrations performed on one day could be used with accuracy to derive volumes > 0.1 microliter collected on subsequent days, when using the same machine (s.d. for residuals plot = 2.49 Periotron units), but this was not the case for different machines (s.d. = 9.57 Periotron units). Varying serum protein concentration by up to 500% had a negligible effect on calculated volumes above 0.1 microliter. We conclude that the Periotron 8000 is at least as reliable a machine as the Periotron 6000, and that the calibration lines for both machines are best described using 4th order polynomial regression equations and "look-up" tables, rather than quadratic (Periotron 6000) or the manufacturer's software (Periotron 8000). Serum seems to be an acceptable GCF substitute for calibrations, which can be performed 1 day, and used on subsequent days for a given machine and for volumes above 0.1 microliter.This paper reports the detailed calibration of the new Periotron 8000 with different fluids and uses the method of least squares to derive polynomial regression equations up to the 6th order, to investigate the most accurate descriptor of the resulting calibration lines. The use of a 4th order polynomial regression equation (recommended by the manufacturer) provided better coefficients of determination (R2: 0.999) and root mean square errors (RMSE = 1.6) than either linear regression (R2: 0.986, RMSE = 10.9) or quadratic models (R2: 0.998, RMSE = 3.2). Data derived using the manufacturer's MLCONVERT software program lacked accuracy and incurred large errors for volumes > 0.5 microliter. Calibrations performed on one day could be used with accuracy to derive volumes > 0.1 microliter collected on subsequent days, when using the same machine (s.d. for residuals plot = 2.49 Periotron units), but this was not the case for different machines (s.d. = 9.57 Periotron units). Varying serum protein concentration by up to 500% had a negligible effect on calculated volumes above 0.1 microliter. We conclude that the Periotron 8000 is at least as reliable a machine as the Periotron 6000, and that the calibration lines for both machines are best described using 4th order polynomial regression equations and "look-up" tables, rather than quadratic (Periotron 6000) or the manufacturer's software (Periotron 8000). Serum seems to be an acceptable GCF substitute for calibrations, which can be performed 1 day, and used on subsequent days for a given machine and for volumes above 0.1 microliter.
This paper reports the detailed calibration of the new Periotron 8000® with different fluids and uses the method of least squares to derive polynomial regression equations up to the 6th order, to investigate the most accurate descriptor of the resulting calibration lines. The use of a 4th order polynomial regression equation (recommended by the manufacturer) provided better coefficients of determination ( R 2 : 0.999) and root mean square errors (RMSE = 1.6) than either linear regression ( R 2 : 0.986, RMSE = 10.9) or quadratic models ( R 2 : 0.998, RMSE = 3.2). Data derived using the manufacturer's MLCONVERT software program lacked accuracy and incurred large errors for volumes > 0.5 μl. Calibrations performed on one day could be used with accuracy to derive volumes >0.1 μl collected on subsequent days, when using the same machine (s.d. for residuals plot=2.49 Periotron units), but this was not the case for different machines (s.d. = 9.57 Periotron units). Varying serum protein concentration by up to 500% had a negligible effect on calculated volumes above 0.1 μl. We conclude that the Periotron 8000® is at least as reliable a machine as the Periotron 6000®, and that the calibration lines for both machines are best described using 4th order polynomial regression equations and “look‐up” tables, rather than quadratic (Periotron 6000®) or the manufacturer's software (Periotron 8000®). Serum seems to be an acceptable GCF substitute for calibrations, which can be performed 1 day, and used on subsequent days for a given machine and for volumes above 0.1 μl.
This paper reports the detailed calibration of the new Periotron 8000® with different fluids and uses the method of least squares to derive polynomial regression equations up to the 6th order, to investigate the most accurate descriptor of the resulting calibration lines. The use of a 4th order polynomial regression equation (recommended by the manufacturer) provided better coefficients of determination (R2: 0.999) and root mean square errors (RMSE = 1.6) than either linear regression (R2: 0.986, RMSE = 10.9) or quadratic models (R2: 0.998, RMSE = 3.2). Data derived using the manufacturer's MLCONVERT software program lacked accuracy and incurred large errors for volumes > 0.5 μl. Calibrations performed on one day could be used with accuracy to derive volumes >0.1 μl collected on subsequent days, when using the same machine (s.d. for residuals plot=2.49 Periotron units), but this was not the case for different machines (s.d. = 9.57 Periotron units). Varying serum protein concentration by up to 500% had a negligible effect on calculated volumes above 0.1 μl. We conclude that the Periotron 8000® is at least as reliable a machine as the Periotron 6000®, and that the calibration lines for both machines are best described using 4th order polynomial regression equations and “look‐up” tables, rather than quadratic (Periotron 6000®) or the manufacturer's software (Periotron 8000®). Serum seems to be an acceptable GCF substitute for calibrations, which can be performed 1 day, and used on subsequent days for a given machine and for volumes above 0.1 μl.
This paper reports the detailed calibration of the new Periotron 8000 with different fluids and uses the method of least squares to derive polynomial regression equations up to the 6th order, to investigate the most accurate descriptor of the resulting calibration lines. The use of a 4th order polynomial regression equation (recommended by the manufacturer) provided better coefficients of determination (R2: 0.999) and root mean square errors (RMSE = 1.6) than either linear regression (R2: 0.986, RMSE = 10.9) or quadratic models (R2: 0.998, RMSE = 3.2). Data derived using the manufacturer's MLCONVERT software program lacked accuracy and incurred large errors for volumes > 0.5 microliter. Calibrations performed on one day could be used with accuracy to derive volumes > 0.1 microliter collected on subsequent days, when using the same machine (s.d. for residuals plot = 2.49 Periotron units), but this was not the case for different machines (s.d. = 9.57 Periotron units). Varying serum protein concentration by up to 500% had a negligible effect on calculated volumes above 0.1 microliter. We conclude that the Periotron 8000 is at least as reliable a machine as the Periotron 6000, and that the calibration lines for both machines are best described using 4th order polynomial regression equations and "look-up" tables, rather than quadratic (Periotron 6000) or the manufacturer's software (Periotron 8000). Serum seems to be an acceptable GCF substitute for calibrations, which can be performed 1 day, and used on subsequent days for a given machine and for volumes above 0.1 microliter.
Author Landini, G.
Patel, N. C.
Chapple, I. L. C.
Ward, R. S. N.
Griffiths, G. S.
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  surname: Landini
  fullname: Landini, G.
  organization: Oral Diseases Research Group, The University of Birmingham, School of Dentistry
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  surname: Griffiths
  fullname: Griffiths, G. S.
  organization: Department of Periodontology, The Eastman Dental institute, London, UK
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  givenname: N. C.
  surname: Patel
  fullname: Patel, N. C.
  organization: Oral Diseases Research Group, The University of Birmingham, School of Dentistry
– sequence: 5
  givenname: R. S. N.
  surname: Ward
  fullname: Ward, R. S. N.
  organization: Department of Periodontology, The Eastman Dental institute, London, UK
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Issue 2
Keywords Human
Periodontal disease
Equipment
Stomatology
Pathogenesis
Technology
Calibration equipment
Exploration
Early
Diagnosis
Language English
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PublicationTitle Journal of periodontal research
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References_xml – reference: Preshaw PM, Kelly PJ, Heasman PA. Quadratic calibration curves for the Periotron 6000®. J Periodont Res 1996; 31: 441-443.
– reference: Chapple ILC, Cross IA, Glenwright HD, Matthews JB. Calibration and reliability of the Periotron 6000® for individual gingival crevicular fluid samples. J Periodont Res 1995; 30: 73-79.
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Snippet This paper reports the detailed calibration of the new Periotron 8000® with different fluids and uses the method of least squares to derive polynomial...
This paper reports the detailed calibration of the new Periotron 8000 with different fluids and uses the method of least squares to derive polynomial...
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StartPage 79
SubjectTerms Biological and medical sciences
Calibration
Dental Equipment - standards
Equipment Design
GCF volume
Gingival Crevicular Fluid
Humans
Investigative techniques, diagnostic techniques (general aspects)
Least-Squares Analysis
Medical sciences
Miscellaneous. Technology
Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques
Periodontics - instrumentation
Periotron 6000
Periotron 8000
polynomial regression
reliability
Reproducibility of Results
Title Calibration of the Periotron 8000® and 6000® by polynomial regression
URI https://api.istex.fr/ark:/67375/WNG-ZNPNHJZZ-J/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1600-0765.1999.tb02226.x
https://www.ncbi.nlm.nih.gov/pubmed/10207836
https://www.proquest.com/docview/69700981
Volume 34
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