Professional Reference articles are written by UK doctors and are based on research evidence, UK and European Guidelines. They are designed for health professionals to use, so you may find the language more technical than the condition leaflets.
A low level of blood phosphate is defined as a level below 0.8 mmol/L (the normal range should be given by the assaying laboratory but is about 0.8 to 1.4 mmol/L in adults and slightly higher in children). Significant hypophosphataemia (below 0.4 mmol/L) may occur due to redistribution into cells, renal losses or decreased intake. Patients with low phosphate often also have other electrolyte deficiencies.
A normal diet contains plenty of phosphate, as it is present in all living organisms. Normal dietary intake is usually about 700-1250 mg a day and 40-80% is absorbed in the intestinal tract.Normally the majority of this is reabsorbed by the renal tubular cells. Vitamin D increases uptake, and homeostasis in terms of bone content of phosphate and renal excretion is controlled by vitamin D, parathyroid hormone (PTH), and fibroblast growth factor 23 (FGF 23).
- Inadequate intake:
- Poor intake may be due to poor diet, including eating disorders such as anorexia nervosa, difficulty with chewing and swallowing, and alcoholism.
- Malnutrition due to malabsorption or persistent vomiting.
- The severely ill patient is most at risk when they start to recover and move from a catabolic state to an anabolic state.
- Vitamin D deficiency.
- Gut phosphate binders - eg, aluminium hydroxide.
- Increased renal excretion:
- Hyperparathyroidism: PTH reduces reabsorption by the proximal renal tubule.
- High salt load causes reduced reabsorption of sodium by the proximal tubule but also reduced phosphate reabsorption.
- Vitamin D deficiency, including hypophosphataemic rickets.
- Renal tubular disorders, including Fanconi's syndrome, Dent's disease.
- Hypophosphataemia is common after renal transplantation especially after long periods of dialysis.
- Drugs causing renal phosphate leak, including aminoglycosides, cisplatin and tenofovir.
- Heavy metal poisoning and paraproteinaemias by impairing renal tubule function.
- Oncogenic osteomalacia is a paraneoplastic syndrome of osteomalacia, hypophosphataemia, renal phosphate loss, bone pain, and muscle weakness. It is caused by excessive synthesis and secretion of FGF23, a phosphaturic hormone that is normally produced by osteocytes.Several tumours can cause this but most are benign tumours of mesenchymal origin.
- Move from extracellular to intracellular compartment:
- Treatment of diabetic ketoacidosis (insulin drives phosphate into cells).
- Refeeding syndrome - carbohydrate refeeding after fasting. Other risks of refeeding include low potassium, low magnesium, low calcium and abnormal glucose metabolism.[1, 5]
- Acute respiratory alkalosis.
- The hungry bone syndrome (increased uptake by bone matrix) which occurs after parathyroidectomy.
- Leukaemia or lymphomas.
- Hypophosphataemia is rare in the general population but relatively common in hospitalised patients (2.2-3.1%) and higher still in those on intensive care units (28.8-33.9%), those with sepsis (65-80%), those with chronic alcoholism (2.5-30.4%), those with major trauma (75%) and those with chronic obstructive pulmonary disease (COPD) (21%).
- Hypophosphataemia is more likely in alcoholism, diabetic ketoacidosis, burns and sepsis. It is a feature of X-linked hypophosphataemic rickets. This is rare, occurring in 1 in 20,000 live births.
- In adolescents it is often due to eating disorders but in older people it tends to be associated with alcoholism, malignancy or vitamin D deficiency.
- Chronic or mild hypophosphataemia may be asymptomatic (phosphate levels 0.6-0.8 mmol/L).Most patients with hypophosphataemia have no specific symptoms or perhaps fatigue.
- Muscle weakness (diaphragmatic, cardiac and skeletal), bone pain, rhabdomyolysis, and altered mental status (confusion, hallucinations) are the most common presenting features.
- Severe acute hypophosphataemia (level <0.3 mmol/L) may present with disorientation, seizures, focal neurological deficits, congestive heart failure, and muscle pain.
- Syndromes of chronic phosphate loss usually present with bone pain, muscular weakness and skeletal disorders.
- Markedly low phosphate with bone pain and excessive phosphate loss in urine in an adult suggests an oncogenic osteomalacia.
- There are usually no physical signs.
- If hypophosphataemia starts in childhood, there is usually short stature and perhaps bowed legs from rickets.
- In adults, firm palpation of bones may show tenderness.
- Hepatomegaly may indicate chronic alcoholism or underlying malignancy.
- Calcium, phosphate, magnesium, plasma proteins - in the presence of low phosphate:
- High calcium suggests hyperparathyroidism.
- Low calcium suggests lack of vitamin D or malabsorption, or hungry bone syndrome.
- Low magnesium suggests dietary deficiency.
- Consider paraproteinaemia if high globulins, severe hypophosphataemia with suspicious features such as anaemia, bone pain, renal dysfunction or hypercalcaemia.
- Renal function and electroytes: renal tubular disease or extra renal causes commonly cause electrolyte disturbance.
- LFTs: may show elevated alkaline phosphatase in chronic hypophosphataemia due to osteomalacia. They may also indicate chronic alcoholism.
- PTH and vitamin D levels.
- If respiratory alkalosis is considered, arterial blood gases are required.
- If renal loss is considered, fasting morning urine for phosphate content, along with blood sample.
- If Fanconi's syndrome is considered, obtain plasma bicarbonate and urate and test urine for glucose and amino acids. A full Fanconi's syndrome consists of renal glycosuria, aminoaciduria, renal tubular acidosis, low blood urate due to high urinary loss, and excessive urinary loss of phosphate.
- X-rays can help evaluate osteopenia, osteomalacia, or hyperparathyroidism. Looser zones suggest osteomalacia. Erosions of the distal phalanges and clavicles and circular punched-out lesions in the long bones are typical of primary hyperparathyroidism.
- Bone scintigraphy may demonstrate increased uptake at multiple areas in cases of severe osteomalacia,
- Ultrasound of the neck may help identify enlarged parathyroid glands but technetium 99mTc scanning can be more accurate and easier to locate ectopic glands.
- Dual-energy X-ray absorptiometry (DEXA) bone density scan: chronic phosphate deficiency will cause loss of bone density.
- If X-rays are inconclusive, bone biopsy may be required.
Mild hypophosphataemia often resolves without treatment but severe hypophosphataemia may cause diaphragmatic weakness requiring artificial ventilation.
- Treatment is dependent upon cause, severity and duration.
- Treatment should address the underlying cause where possible.
- Patients should be referred to a specialist if:
- The cause is uncertain.
- Hypophosphataemia is chronic or severe (phosphate <0.3 mmol/L).
- They are symptomatic.
- There is short stature or there are skeletal deformities consistent with rickets.
- There is a family history of skeletal deformities or hypophosphataemia.
- Phosphate supplements:
- Phosphate supplements should be given where hypophosphataemia may be anticipated, as in refeeding after anorexia, starvation or alcoholism.
- Usually oral phosphate is well tolerated although very high doses may cause diarrhoea.
- Where there is an acute situation or lack of intestinal function, parenteral phosphate may be used but this is much more dangerous and requires monitoring of calcium, phosphate and electrolyte levels every six hours as response is unpredictable. It should only used where serum phosphate levels are under 1.5 mmol/L. The risk is severe hypocalcaemia which may be life-threatening, or over-treatment resulting in hyperphosphataemia and hyperkalaemia. Patients with poor renal function are at higher risk from intravenous treatment.
- In coeliac disease or Crohn's disease the underlying disease should be treated but vitamin D supplements may be required.
- Oral phosphate supplements may be beneficial in genetic disorders that lead to urinary phosphate loss although they do not correct the underlying abnormality. Monitor blood calcium and phosphate, bone density and growth.
- In oncogenic osteomalacia, phosphate supplements are useful until the tumour has been identified and removed.
- Vitamin D deficiency is usually treated with oral vitamin D but in severe renal disease the kidneys may be unable to convert hepatic 24 hydroxyvitamin D3 to 1,25 dihydroxyvitamin D3 and so this form may need to be given.
- Hyperparathyroidism requires identification and removal of the offending tumour.
- Problems such as alcoholism and eating disorders require appropriate intervention.
- Congenital phosphate wasting syndromes require long-term supplementation.
- To reduce the risk of hypophosphataemia, patients having renal transplantation may be considered for parathyroidectomy before transplant surgery, or more recently the calcimimetic agent cinacalcet has been shown to improve phosphate levels.[9, 10, 11]
- Patients with diabetic ketoacidosis are at high risk of developing hypophosphataemia but parenteral phosphate does not appear to improve outcome.
- Acute hypophosphataemia can produce seizures, delirium, coma, or focal neurological findings.
- There may be heart failure, rhabdomyolysis, acute haemolysis, leukocyte dysfunction, and abnormal LFTs.
- Heart failure, rhabdomyolysis, and haemolysis can produce acute kidney injury.
- Leukocyte dysfunction increases susceptibility to infection.
- They can also exhibit platelet dysfunction, glucose intolerance, and metabolic acidosis.
- Chronic hypophosphataemia due to phosphate loss causes mostly bone pathology.
- In children, rickets leads to short stature and bony deformities with abnormal bone mineralisation.
- Adults may develop osteomalacia with severe bone pain and fractures.
- Correction of acute hypophosphataemia tends to leave no long-term complications but failure to recognise and treat an acute, severe situation can lead to fatality.
- X-linked hypophosphataemia rickets and vitamin D-resistant rickets are only incompletely treatable and result in lifelong skeletal deformities.
- Whether hypophosphataemia itself increases mortality is difficult to ascertain, as many of the patients are critically unwell from the cause of the low phosphate.
Those at high risk, such as renal dialysis and transplant patients, those with eating disorders, and patients who have just had parathyroidectomy, should be monitored and given appropriate oral or parenteral supplementation if required.
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Further reading & references
- Hypophosphatemic Rickets, X-linked Dominant, XLHR; Online Mendelian Inheritance in Man (OMIM)
- Hypophosphatemic Rickets, Autosomal Dominant, ADHR; Online Mendelian Inheritance in Man (OMIM)
- Alon US, Levy-Olomucki R, Moore WV, et al; Calcimimetics as an adjuvant treatment for familial hypophosphatemic rickets. Clin J Am Soc Nephrol. 2008 May 3(3):658-64. doi: 10.2215/CJN.04981107. Epub 2008 Feb 6.
- Manning S, Gilmour M, Weatherall M, et al; Refeeding syndrome is uncommon in alcoholics admitted to a hospital detoxification unit. Intern Med J. 2014 May 44(5):512-4. doi: 10.1111/imj.12408.
- Bergwitz C, Juppner H; FGF23 and syndromes of abnormal renal phosphate handling. Adv Exp Med Biol. 2012 728:41-64. doi: 10.1007/978-1-4614-0887-1_3.
- NDR (Nutrition and Diet Resources) UK
- Glendenning P, Bell DA, Clifton-Bligh RJ; Investigating hypophosphataemia. BMJ. 2014 May 28 348:g3172. doi: 10.1136/bmj.g3172.
- Kalantar-Zadeh K, Gutekunst L, Mehrotra R, et al; Understanding sources of dietary phosphorus in the treatment of patients with chronic kidney disease. Clin J Am Soc Nephrol. 2010 Mar 5(3):519-30. doi: 10.2215/CJN.06080809. Epub 2010 Jan 21.
- Bergwitz C, Juppner H; Regulation of phosphate homeostasis by PTH, vitamin D, and FGF23. Annu Rev Med. 2010 61:91-104. doi: 10.1146/annurev.med.051308.111339.
- Leaf DE, Pereira RC, Bazari H, et al; Oncogenic osteomalacia due to FGF23-expressing colon adenocarcinoma. J Clin Endocrinol Metab. 2013 Mar 98(3):887-91. doi: 10.1210/jc.2012-3473. Epub 2013 Feb 7.
- Skipper A; Refeeding syndrome or refeeding hypophosphatemia: a systematic review of cases. Nutr Clin Pract. 2012 Feb 27(1):34-40. doi: 10.1177/0884533611427916.
- Witteveen JE, van Thiel S, Romijn JA, et al; Hungry bone syndrome: still a challenge in the post-operative management of primary hyperparathyroidism: a systematic review of the literature. Eur J Endocrinol. 2013 Feb 20 168(3):R45-53. doi: 10.1530/EJE-12-0528. Print 2013 Mar.
- Brunelli SM, Goldfarb S; Hypophosphatemia: clinical consequences and management. J Am Soc Nephrol. 2007 Jul 18(7):1999-2003. Epub 2007 Jun 13.
- Imel EA, Econs MJ; Approach to the hypophosphatemic patient. J Clin Endocrinol Metab. 2012 Mar 97(3):696-706. doi: 10.1210/jc.2011-1319.
- Morales E, Gutierrez E, Andres A; Treatment with calcimimetics in kidney transplantation. Transplant Rev (Orlando). 2010 Apr 24(2):79-88. doi: 10.1016/j.trre.2010.01.001.
- Messa P, Cafforio C, Alfieri C; Calcium and phosphate changes after renal transplantation. J Nephrol. 2010 Nov-Dec 23 Suppl 16:S175-81.
- Kim YJ, Kim MG, Jeon HJ, et al; Clinical manifestations of hypercalcemia and hypophosphatemia after kidney transplantation. Transplant Proc. 2012 Apr 44(3):651-6. doi: 10.1016/j.transproceed.2011.12.050.
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