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The Pharmaceutical Journal
Vol 268 No 7180 p3-8
5/12 January 2002

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High vitamin A intake increases risk of hip fractures

A diet rich in retinol (vitamin A) increases the risk of hip fractures in postmenopausal women, researchers have confirmed.

Dr Diane Feskanich, Brigham and Women's Hospital, Boston, Massachusetts, and colleagues speculated that long-term consumption of high levels of vitamin A might contribute to osteoporosis and hip fractures. They looked at the relationship between vitamin A intake from foods and supplements and risk of hip fracture in 72,337 postmenopausal women taking part in the Nurses' Health Study in the United States.

The researchers found that for women consuming the most vitamin A (3,000µg of retinol equivalents per day or more) compared with those consuming the least (less than 1,250µg per day), the relative risk of hip fracture was 1.48 (95 per cent confidence interval, 1.05–2.07, P=0.003). They say that the increased risk was primarily attributable to retinol and that beta-carotene did not contribute significantly to fracture risk. The association between high retinol intake and fracture risk was attenuated among women using postmenopausal oestrogens, they say.

In an accompanying editorial (ibid, p102), Dr Margo Denke, Centre for Human Nutrition, University of Texas, Dallas, said: "The findings of Feskanich et al provide further support for [determining] a safe upper limit for dietary retinol." She comments that the observation that risk of hip fracture was higher among women not taking oestrogens was intriguing. "Oestrogens are known to block several steps in osteoclast function, including differentiation, activation, and programmed cell death, supporting the possibility that oestrogen could oppose the type of effects expected of retinoic acid [a metabolite of retinol]." She concludes: "This study serves as a reminder that vitamins are potent, essential nutrients which have effects that can precipitate harm as well as provide benefit."

Correction
This study was published in the JAMA (2002;287:47).

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