Precision of Measurement As A Component of
Precision of Measurement As A Component of
Precision of Measurement As A Component of
net/publication/6393791
CITATIONS READS
146 639
2 authors:
All content following this page was uploaded by Nick Mascie-Taylor on 01 March 2016.
Abstract This paper describes the main quality control Variance Components
methods for determining human observer measurement error
and instrument error focusing on intra-observer and inter- Usually for a continuous (quantitative) trait such as weight
observer technical error of measurements (TEMs) and relative or height the variance (s2) or standard deviation (s) would be
TEM, and the coefficient of reliability (R). R values above 0.95 the statistic of choice to quantify the extent of the variation
are indicative of small errors. To compare variances between (Zar, 1999). Suppose, for example, the variance in weight of a
different variables, the coefficient of variation, a measure of random sample was determined. It would be erroneous to
relative variability, is used. The total variation of a character assume that this calculated variance necessarily reflected the
can be partitioned into genetic, environmental, and error ‘real’ variance of the character under investigation. This
components. Determination of the genetic component of depends on how precisely the weight is measured. In other
variation (heritability) is usually obtained from twin studies or words, errors may occur because of human measurement error
other family studies. A good environment improves the or through instrument error.
population mean, whereas a poor environment can lower the
population mean without any change in the underlying genetic Thus, ‘Total’ variance‘Real’ varianceHuman measurement
structure. Worked examples of how to calculate TEM, R, and errorInstrument error.
heritability are provided. J Physiol Anthropol 26(2): 253–256, Measuring the magnitude of these errors is a major element
2007 http://www.jstage.jst.go.jp/browse/jpa2 of quality control.
[DOI: 10.2114/jpa2.26.253]
Quality Control Determination
Keywords: quality control, technical error of measurement,
coefficient of reliability, heritability Human measurement error
Human measurement error or observer measurement error is
indicative of whether research assistants measure a trait
Introduction consistently. Imagine that ten children have had their weight
and height independently measured by two research assistants
The study of similarities and differences between human (A and B) as shown in Table 1.
populations has been investigated by scientists for centuries,
and the notion of different human races derived from the Table 1 Weights and heights (recumbent length) of 10 children
incorrect supposition that there was greater variation between measured by two assistants, A and B (Goto, 2006)
populations than within populations (Cavalli-Sforza and
Weight (kg) Height (cm)
Bodmer, 1971). Nowadays it is widely acknowledged that Child
upwards of 95% of the variation of a trait is within a Number
Assistant A Assistant B Assistant A Assistant B
population and only 5–10% of the variation is between
populations (Cavalli-Sforza and Bodmer, 1971). These within 1 5.50 5.45 64.50 64.00
2 7.70 7.60 71.00 71.50
and between population differences reflect underlying genetic
3 5.35 5.35 58.00 59.00
and environmental variation. However, if errors have occurred 4 5.00 5.05 58.00 58.00
in the measurement of the trait under consideration (either due 5 8.95 8.95 70.50 71.50
to instrument or human measurement errors), these can 6 6.15 6.15 69.00 67.50
compromise many statistical methods and may falsify the 7 6.70 6.75 63.00 64.00
8 5.85 5.85 65.00 64.50
partitioning into genetic and environmental components.
9 7.35 7.35 62.00 62.00
10 6.95 6.95 68.00 68.00
254 Precision of Measurement
where N is the sample size, K the number of assistants, and M As a measure of variability, the variance (and, of course,
the measurement, and M(n) is the nth replicate of measurement standard deviation) have magnitudes which are dependent on
(see Ulijaszek and Lourie, 1994 for a review of anthropometric the magnitude of the data. For example, elephants have ears
measurement error). that are 100 times larger than those of mice. If elephant ears
It is also possible to compute the relative TEM (%TEM), were no more variable, relative to their size, than mouse ears,
which provides an estimate of the error magnitude relative to relative to their size, the standard deviation of elephant ear
the size of the measurement (expressed as a percentage) and is lengths would be 100 times as great as the standard deviation
analogous to the coefficient of variation (see below). of mouse ear lengths—and the variance of the former would be
10,000 times (1002) the variance of the latter! The coefficient
of variation (CV) expresses sample variability relative to the
Goto, R and Mascie-Taylor, CGN J Physiol Anthropol, 26: 253–256, 2007 255
Table 2 Absolute (SD) and relative (CV) variability of height, weight, differences of the character within each type of twin pair. So,
plasma albumin, and haemoglobin concentrations from the for example, a USA study (Newman et al., 1937) found that
longitudinal study (Goto, 2006)
the variance of the difference in stature between dizygotic
Variable Mean SD CV (%) twins was 14.79, and for monozygotic twins 2.61. So,
VDZ VMZ (V V )VE VG
Height (cm) 67.28 4.89 7.27 h2 ≡ G E
Weight (kg) 7.06 1.20 17.00 VDZ VG VE VT
Plasma albumin (g/l) 42.37 7.00 16.52
Haemoglobin (g/l) 91.83 12.57 13.68 14.792.61 12.18
h2 0.82
14.79 14.79
mean of the sample. Thus 82% of the stature variation in dizygotic twins is due to
genetic differences and 18% to the environment.
SD *100
CV Just because the heritability is high does not imply that the
X mean value for a character cannot change. If individuals are
The coefficient of variation may be calculated only for ratio brought up in a poor environment they will be smaller than
scales (i.e., those with a true zero value). It is not valid to their genetic potential. For example, when Japanese migrants
calculate coefficients of variation for interval scales (e.g., to Hawaii and their first generation descendants were
temperature data using the Celsius Scale, or z-scores of height- compared, the descendants were over 4 cm taller (Shapiro,
for-age or weight-for-height). 1939), presumably because of the better environmental
Table 2 presents information on the mean and standard conditions in Hawaii at that time, compared with Japan. In
deviation (SD) for 4 nutritional variables. The standard developing countries the average stature and weight of adults is
deviation of haemoglobin is more than 10 times larger than the generally lower than in developed countries. These reductions
SD for weight, but after computation of the coefficient of are not caused by genetic factors. Rather, the poor environment
variation, weight has a larger CV than height (because the (food insecurity and poor nutritional intake, and high levels of
mean height is so much larger that the mean weight). Simpson infectious disease and stress) leads to child growth retardation
et al. (1960) present a good discussion of the coefficient of that starts as early as 3 months of age and continues
variation and its biological applications. throughout life.
Assuming that quality control has been good, what are the High levels of error can render statistical comparisons
causes of variation of trait within a population? Geneticists invalid, and errors can artificially inflate the variance
partition the variation of a trait into various components. associated with a particular measurement (Bailey and Byrnes,
Simplistically (ignoring errors):- 1990). Furthermore, empirical data have shown the
measurement error can compromise a wide variety of
Total Variation (VT)Genetic Variation (VG) univariate and multivariate statistical methods, particularly
Environmental Variation (VE) those that rely on correlation, regression, and covariance (Liu,
1988; Bailey and Byrnes, 1990). Good quality control,
and heritability (h2)VG/VT. Heritability defines the involving both reduction in instrumentation and human
proportion of the total variation accounted for by genetic measurement error, are therefore prerequisites for increased
differences between people within a population. Heritability precision and improved interpretation of results.
ranges from 0 (all variation environmental) to 1 (all variation A number of methods of measuring inconsistency are
due to genetic factors). More complicated formulations include available but the preferred method involves calculation of
taking into account, for example, genotype-environment either intra- or inter-technical error of measurement (TEM)
interactions and correlations (see Plomin et al., 2001 for a full initially, relative TEM, and then the coefficient of reliability
discussion). (Ulijaszek and Kerr, 1999). TEM gives information on the
Twin studies, comparison of non-identical (dizygotic, DZ) error margin of a trait and therefore is an accuracy index.
and identical (monozygotic, MZ) twin pairs, and other family Determination of acceptable levels of measurement errors are
studies, yield heritabilities of weight between 0.5 and 0.75 and not straightforward and relate to the variable being studied as
height between 0.7 and 0.9 (Cavalli-Sforza and Bodmer, 1971), well as the age of the subjects (Ulijaszek and Kerr, 1999).
suggesting that between 50% and 75% of the variance in Even so, coefficients of reliabilities above 0.95 are indicative
weight is caused by inheritance (nature), and only 25% to 50% of good quality control.
by the environment (nurture). Trait variation within and between populations results from
For twins, heritability can be calculated using the formula genetic differences between people as well as environmental
shown below, where VDZ and VMZ refer to the variance of the effects. Although determination of the genetic component
256 Precision of Measurement