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Editorial

See corresponding article on page 257.

Does milk intake in childhood protect against later osteoporosis?1,2


Katherine L Tucker

The importance of the intake during childhood and adolescence Despite limitations in data availability, the study results are
of dietary calcium, which in the United States is derived largely compelling. Milk intake during childhood and adolescence was
from milk and dairy products, to the risk of osteoporotic fractures associated with BMC and BMD of the hip both in women aged
in later life is generally assumed to be fact. Many studies have 2049 y (n = 1371) and in those aged 50 y (n = 1880). Younger
shown the contribution of calcium intake during development to adult women who consumed < 1 serving of milk/wk during child-
the accretion of peak bone mass, which is assumed to be a criti- hood had BMC 5.6% lower than that in younger adult women
cal factor in later-life osteoporosis. However, relatively few stud- who consumed > 1 serving/d. The results for hip BMC and BMD
ies have shown a direct link between early diet and later risk of were similarly significant by earlier milk-intake category for

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osteoporosis. Indeed, the effect of early calcium intake on later women aged 50 y. Furthermore, low milk intake during child-
risk has been questioned, because follow-up observations after hood was associated with a 2-fold greater risk of fracture among
calcium supplementation trials usually showed that benefits older women, with significant associations between both child-
regress when the supplements are no longer consumed (1). This hood and adolescent milk intakes and greater incidence of life-
finding raises the question of whether the contribution of high cal- time fracture. The authors estimate that low milk intake during
cium intake in childhood persists into older age, when fracture childhood was associated with 11% of osteoporotic fractures in
risk accelerates. women later in life.
Studies that examined milk or calcium intake in childhood in One of the important considerations in the study by Kalkwarf et
relation to later bone mineral density (BMD) or fracture relied on al was that current milk intake was adjusted, which partially
recalled data, and the results are inconsistent. Several studies removed the effect of the tendency of women who consumed more
reported positive associations between earlier reported milk or cal- milk in childhood to do the same in adulthood. Earlier intake
cium intake and BMD in premenopausal women, but several other remained significant, despite a positive association between cur-
studies did not find this association. Very few studies examined rent adult dietary calcium intake and BMC and BMD. The statis-
early calcium intake and subsequent BMD or fractures in older tical models were designed to control for important potential con-
women. A retrospective study of elderly patients with osteoporo- founders. The adjustment for current calcium intake may have been
sis and of healthy control subjects found that recalled milk con- limited by the fact that it was based on a single 24-h recall. How-
sumption during childhood and adolescence was significantly ever, calcium intake generally has a relatively low ratio of intra- to
associated with later bone status, although knowledge of the prior interindividual variance, because of regular patterns of milk usage.
diagnosis may have contributed to recall bias (2). Two studies of The use of recall for data on milk consumption during child-
postmenopausal women (aged 6079 y) also found significant hood and adolescence has several limitations, particularly in
associations between reported milk intake in childhood or adoles- women with osteoporotic fracture. There is the possibility of recall
cence (or both) and BMD, but no correction was made for current bias among those who know that they have been diagnosed with
intake (3, 4). Fewer studies investigated childhood milk or cal- osteoporosis. However, this factor is less likely to affect BMD or
cium intake and later adult fractures, and the results among these BMC results. Furthermore, much of the error associated with the
studies are mixed. The largest of them, a 12-y prospective follow- recall of milk consumption during childhood and adolescence is
up (5) using data from the Nurses Health Study, found no associ- likely to be due to random error in memory, which may weaken
ation between reported milk intake in adolescence and fracture. the ability to see associations. Another important limitation of
In this issue of the Journal, Kalkwarf et al (6) present data from these data is that they cannot describe intakes greater than 1 glass
3251 non-Hispanic, white female participants (aged 20 y) in the per day. More than 84% of women reported consumption of at
nationally representative third National Health and Nutrition least one glass of milk per day during childhood and 70% reported
Examination Survey (NHANES III), in which adult women were similar consumption during adolescence. The fact that associa-
asked about the frequency of their milk consumption during child- tions between childhood and adolescent milk intakes and adult
hood (ages 512 y) and adolescence (ages 1317 y). Kalkwarf et fracture risk were detected despite this truncation is noteworthy,
al studied the association of BMD and bone mineral content and the true associations may have been even stronger.
(BMC) as well as reported histories of fracture after age 13 y
(lifetime fracture) and after age 50 y (osteoporotic fracture) with 1
From the Jean Mayer US Department of Agriculture Human Nutrition
these reported milk-intake frequencies in regression analyses. Research Center on Aging at Tufts University, Boston.
They found that earlier reported milk intake was associated with 2
Address reprint requests to KL Tucker, Jean Mayer USDA Human Nutri-
apparent protection against later fracture as well as with greater tion Research Center on Aging at Tufts University, 711 Washington Street,
bone mass. Boston, MA 02111. E-mail: katherine.tucker@tufts.edu.

10 Am J Clin Nutr 2003;77:101. Printed in USA. 2003 American Society for Clinical Nutrition
EDITORIAL 11

It is interesting that current dietary calcium intake from food potential for future effects of diminished milk intake on bone sta-
was more consistently associated with bone measures than was tus and risk of fracture.
dietary calcium intake plus calcium from supplements or antacids.
Possibly, some current supplement use is stimulated by a diagno-
sis of osteoporosis or a previous fracture. This observation also REFERENCES
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improvements with calcium supplement interventions tended to Dawson-Hughes B, Heaney R, eds. Nutritional aspects of osteoporo-
regress once the supplement was removed. As noted by the sis. San Diego: Academic Press, 2001:10723.
authors, it is significant that milk contains not only calcium, but 2. Stracke H, Renner E, Knie G, Leidig G, Minne H, Federlin K. Osteo-
also vitamin D, phosphorous, protein, zinc, and magnesium. This porosis and bone metabolic parameters in dependence upon calcium
natural complex of nutrients may have a greater effect on endur- intake through milk and milk products. Eur J Clin Nutr 1993;47:
61722.
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3. Sandler RB, Slemenda CW, LaPorte RE, et al. Postmenopausal bone
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Whereas further investigation into the effect of lifelong dietary
Clin Nutr 1985;42:2704.
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sumption during childhood and adolescence is important. Most of Health 1994;84:131922.
the adult NHANES III participants reported drinking at least one 5. Feskanich D, Willett WC, Stampfer MJ, Colditz GA. Milk, dietary
glass of milk per day during these formative years. In light of both calcium, and bone fractures in women: a 12-year prospective study.
the current tendency in schools to allow beverage choices such as Am J Public Health 1997;87:9927.

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fruit punch rather than milk and of the growing pressure on 6. Kalkwarf HJ, Khoury JC, Lanphear BP. Milk intake during childhood
schools to stock vending machines with soda and other caloric and adolescence, adult bone density, and osteoporotic fractures in US
beverages that lack calcium, attention should be given to the women. Am J Clin Nutr 2003;77:25765.

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