Calcium metabolism or calcium homeostasis is the mechanism by which the body maintains adequate calcium levels. Derangements of this mechanism lead to hypercalcemia or hypocalcemia, which both can have important consequences for health.
Calcium location and quantity
Calcium is the most abundant mineral in the human body. The average adult body contains in total approximately 1 kg, 99% in the skeleton. The extracellular fluid (ECF) contains approximately 22.5 mmol, or which about 9 mmol is in the
serum. Approximately 500 mmol of calcium is exchanged between bone and the ECF over a period of twenty-four hours. (Marshall, 1995).
Normal ranges
The serum level of calcium is closely regulated with a normal
total calcium of 2.2-2.6 mmol/L (9-10.5 mg/dL) and a normal
ionized calcium of 1.1-1.4 mmol/L (4.5-5.6 mg/dL). The amount of total calcium varies with the level of
albumin, a protein to which calcium is bound. The biologic effect of calcium is determined by the amount of
ionized calcium, rather than the total calcium.
Ionized calcium does not vary with the
albumin level, and therefore it is useful to measure the ionized calcium level when the serum albumin is not within normal ranges, or when a calcium disorder is suspected despite a normal total calcium level.
Corrected calcium level
One can derive a
corrected calcium level when the albumin is abnormal. This is to correct for the change in total calcium due to the change in albumin-bound calcium, and gives an estimate of what the calcium level would be if the albumin were within normal ranges.
- Corrected calcium (mg/dL) = measured total Ca (mg/dL) + 0.8 (4.0 - serum albumin *), where 4.0 represents the average albumin level.
When there is hypoalbuminemia (a lower than normal albumin), the corrected calcium level is higher than the total calcium.
Effector organs
Sources
About 25
mmol of calcium enters the body in a normal diet. It can be lower if the diet is low in
milk or other calcium-containing substances. Of this, about 40% (10 mmol) is absorbed in
gut, and 5 mmol leaves the body in feces, netting 5 mmol of calcium a day.
Vitamin D is an important co-factor in the
intestinal absorption of calcium, as it increases the number of
calcium binding proteins, involved in calcium absorption through the
apical membrane of
enterocytes in
small intestine.
Excretion
The
kidney excretes 250 mmol a day in pro-urine, and resorbs 245 mmol, leading to a net loss in the urine of 5 mmol/l. In addition to this, the kidney processes Vitamin D into
calcitriol, the active form that is most effective in assisting intestinal absorption. Both processes are stimulated by
parathyroid hormone (PTH).
The role of bone
Although calcium flow to and from the
bone is neutral, about 5 mmol is turned over a day. Bone serves as an important storage point for calcium, as it contains 99% of the total body calcium. Calcium is released from bone by
parathyroid hormone.
Calcitonin stimulates incorporation of calcium in bone, although this process is largely independent of calcitonin.
Low calcium intake may also be a risk factor in the development of osteoporosis. In one meta-analyses, the authors found that only two out of the 52 studies that they reviewed showed that calcium intake did not promote better bone balance (Heaney, et al). With a better bone balance, the risk of osteoporosis is lowered.
Regulatory organs
The only real regulatory organ is the
parathyroid gland. The parathyroid glands are located behind the
thyroid, and produce parathyroid hormone in response to low calcium levels.
The parafollicular cells of the thyroid produce calcitonin in response to high calcium levels, but its significance is much smaller than that of PTH.
Calcium problems
Hypocalcemia and
hypercalcemia are both serious medical disorders.
Renal osteodystrophy is a consequence of
chronic renal failure related to the calcium metabolism.
Osteoporosis and
osteomalacia have been linked to calcium metabolism disorders.
References
- Heaney, R. P., et al. Calcium, dairy products and osteoporosis. J Am Coll Nutr. 2000 Apr;19(2 Suppl):83S-99S.
- Marshall, W. J. 1995. Clinical Chemistry, 3rd ed. Mosby, London.
External links
Physiology