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Sugar consumption in New Zealand—with Thornley
and McRobbie response
We write in response to Thornley et al’s viewpoint
article The New Zealand sugar (fructose) fountain: time to turn the
tide? published in The New Zealand Medical Journal on 19 March
2010. The data quoted on sugar consumption in New Zealand are presented
misleadingly and are not correctly referenced to primary sources.
The opening two sentences state: “In 2005 New
Zealanders drank and ate, on average, over half a cup (158g) of sucrose (sugar)
per day. In contrast, less than 40g a day (about 1½ tablespoons) are
recommended by the World Health Organization (WHO) to prevent dental caries,
obesity and chronic disease.”
Firstly what is quoted is total sugar intake, not
sucrose intake, as 158g per day. Total sugar intake is not equivalent
to sucrose intake, which is only one type of dietary sugar, along with lactose,
glucose, fructose and maltose.
Secondly, the WHO recommendation is for added
sugars, not total sugars (which includes all sugars naturally present
in foods). The generally accepted definition of added sugars is:
“Sugars and syrups that are added to foods during processing or
preparation. Added sugars do not include naturally occurring sugars such as
those that occur in milk and fruits.”
While it’s not the same thing, data on
sucrose intake are often used a s a proxy for added sugars
intake, since the majority of added sugars come in the form of sucrose in New
Zealand. Comparing our total sugar (not sucrose) intakes with the WHO
recommendation for added sugar (thereby inferring a nearly four fold
difference), and using the terms sucrose and sugar interchangeably is both
inaccurate and confusing. One would expect these terms to describe markedly
different amounts, since the former encompasses sugar intake from all sources
including fruit, vegetables, milk and honey, as well as added sugars.
In addition, the viewpoint article by Simon Thornley
references a key New Zealand paper in this field, that by Parnell et al (Public
Health Nutrition, 2007). The findings on beverages as source of sugar for New
Zealand children are stated, but the author fails to acknowledge some of the key
findings of this research. The paper titled Exploring the relationship
between sugars and obesity, sought to discover the relationship (if any)
between sugar intake and obesity, by analysing data from the 1997 National
Nutrition Survey for Adults and the 2002 Children’s Nutrition Survey. The
researchers found no relationship between current sucrose intake from beverages
(the predominant source of added sugar in children’s diets) and obesity.
Total current sugar intake (but not sucrose) was in fact significantly lower
among obese children compared to children of a normal weight.
Adults and children with the lowest current intakes of sugar
were actually significantly more likely to be overweight or obese. Subsequently,
there was no relationship found between current sugar (sucrose) intake and body
weight status in the New Zealand population. It is acknowledged that as a
cross-sectional study we are unable to equate these findings to sugar and
sucrose intakes over time, however in the absence of longitudinal data for New
Zealand this study is considered to provide credible and valuable information
regarding current intake of sugar and body weight in both adults and
children.
Winsome Parnell
Associate Professor and Registered Dietitian NZ Jane Dodd
Registered Dietitian NZ Donnell Alexander
Registered Dietitian NZ Thornley and McRobbie respond
Parnell and colleagues draw attention to two items raised in
our viewpoint article,1 questioning our
estimates of sugar consumption in New Zealand, and our fidelity in weighing the
evidence linking sugar consumption with obesity.
The first point relates to our estimate of New
Zealander’s sugar consumption of 158g/day. This is derived from UN food
balance sheet data which assesses the national “disappearance” of
food, calculated from production, minus exports, plus imports. What is left is
then considered to have been consumed, although this estimate does not account
for wastage. Our figure was based on the disappearance of the item “sugar
and sweetener's (Total)”, which does not—as Parnell and colleagues
claim—estimate total sugar intake, both added and intrinsic. This figure
estimates the disappearance of added sugar and sweeteners in the food
supply.
We concede that our report was slightly high, and that we
should have restricted our estimate to sugar only, because other sweeteners may
be glucose, fructose or a range of other mono or di saccharides. So our revised
estimate, based on this source, is 50.5 kg/capita/year, or 138 g/day (32
teaspoons per day per person). Notwithstanding the lower figure, this
still indicates that as a nation, we consume added sugar at a rate well
above WHO recommendations and higher than indicated from survey data, based on
self report, as in Parnell’s study.
Parnell’s assessment of New Zealander’s sugar
intakes are lower than food balance sheets.2
However, what is not commonly reported in nutrition studies is that human memory
of both the quantity and nature of food eaten is fallible, with recall estimates
reporting about 20% less sucrose intake compared to more objective
methods.3 This inaccuracy occurs
non-randomly—obese people are more likely to under report consumption than
normal weight people.4 Non-response also
further underestimates food intake. Both sources, however, indicate that the
majority of New Zealanders eat quantities of added sugar far in excess
of the WHO guideline of 40g/day (10 teaspoons per day).
We are then accused of leaving out crucial analytical
results of Parnell’s study, which suggested that obese children report
consuming less sugar than counterparts of normal weight. The study was not
included for specific reasons. First, it employed a cross-sectional design.
Second, it was funded by the sugar industry, and third, it consisted of a
secondary analysis of the data collected for other purposes. All characteristics
have been identified in a meta-analysis which reports a positive association
between soft drink consumption and obesity, as being less likely to report such
a link.5 The weak study design, therefore, lead
us not to include Parnell’s analytical conclusions. Our article, instead,
summarises the evidence of the adverse effects of sugar from either randomised
controlled studies, or meta-analyses (of observational studies). Such designs
are considered stronger than cross-sectional studies for assessing causation.
The consistency of adverse effects, that we observe, linking added sugar,
fructose and sugar-sweetened soft drink intake with obesity, dental decay,
hypertension, insulin resistance and raised serum triglycerides remains.
We concur with Parnell that we have modestly overestimated
national sugar consumption, but disagree that we have misrepresented research
which links sugar intake with adverse health outcomes. In 2009, the American
Heart Association reversed its earlier
position,6 publishing guidelines that advise
severe restriction of added sugar
intake.7
We consider that the potential consequences of this
ubiquitous exposure are too important to narrow our gaze to one cross-sectional
study, sponsored by an industry with a lot to lose.
Simon Thornley
Research Fellow and Lecturer Section of Epidemiology and Biostatistics, School of Population Health Tamaki Campus, University of Auckland, NZ Hayden McRobbie
Senior Clinical Research Fellow Wolfson Institute of Preventive Medicine Queen Mary University of London, London, UK References
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