Not to be confused with Hyperuricemia.
| Hypouricemia |
| Classification and external resources |
Uric acid |
| DiseasesDB |
21432 |
Hypouricemia is a level of uric acid in blood serum that is below normal. In humans, the normal range of this blood component has a lower threshold set variously in the range of 2 mg/dL to 4 mg/dL, while the upper threshold is 530 micromol/L (6 mg/dL) for women and 619 micromol/L (7 mg/dL) for men.[1] Hypouricemia usually is benign and sometimes is a sign of a medical condition.
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Contents
- 1 Causes
- 1.1 Medication
- 1.2 Diet
- 1.3 Genetics
- 1.4 Medical conditions
- 2 Prevalence
- 3 Diagnosis
- 4 Treatment
- 4.1 Drugs and dietary supplements that may be helpful
- 5 Complications
- 6 See also
- 7 References
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Causes
Hypouricemia is not a medical condition itself (i.e., it is benign), but it is a useful medical sign. Usually hypouricemia is due to drugs and toxic agents, sometimes it is due to diet or genetics, and rarely it is due to an underlying medical condition. When one of these causal medical conditions is present, hypouricemia is a common sign.
Medication
The majority of drugs that contribute to hypouricemia are uricosurics (drugs that increase the excretion of uric acid from the blood into the urine).[2] Others include drugs that reduce the production of uric acid: xanthine oxidase inhibitors, urate oxidase (rasburicase), and sevelamer.[3]
Diet
Hypouricemia is common in vegetarians due to the low purine content of most vegetarian diets.[4] Vegetarian diet has been found to result in mean serum uric acid values as low as 239 µmol/L (2.7 mg/dL).[5] While a vegetarian diet is typically seen as beneficial with respect to conditions such as gout,[5] care should be taken to avoid associated health conditions.[citation needed]
Transient hypouricemia sometimes is produced by total parenteral nutrition.[6] Paradoxically, total parenteral nutrition may produce hypouricemia followed shortly by acute gout, a condition normally associated with hyperuricemia.[7][8] The reasons for this are unclear.
Genetics
Genetic mutations known to cause hypouricemia are of two kinds: mutations causing xanthine oxidase deficiency, which reduces the production of uric acid; and mutations causing abnormal kidney function that increases the excretion of uric acid. Collectively known as familial renal hypouricemia, these latter mutations are of two types, involving defects of presecretory and postsecretory reabsorption.
A genetic mutation in Dalmatian dogs causes hypouricemia due to a kidney defect that interferes with reabsorption of uric acid. A similar mutation has been reported in a human brother and sister.[9]
In humans, loss-of-function mutations in the gene URAT1 are associated with presecretory reabsorption defects.[10][11][12]
Medical conditions
Medical conditions that can cause hypouricemia include:
- Fanconi syndrome
- Hyperthyroidism
- Multiple Sclerosis[13]
- Myeloma
- Nephritis
- Wilson's disease
Prevalence
In one study, hypouricemia was found in 4.8% of hospitalized women and 6.5% of hospitalized men. (The definition was less than 0.14 mmol l-1 for women and less than 0.20 mmol l-1 in men.) [14]
Diagnosis
Uric acid clearance should also be performed, increase in clearance points to proximal tubular defects in the kidney, normal or reduced clearance points to a defect in xanthine oxidase.
Treatment
Idiopathic hypouricemia usually requires no treatment. In some cases, hypouricemia is a medical sign of an underlying condition that does require treatment. For example, if hypouricemia reflects high excretion of uric acid into the urine (hyperuricosuria) with its risk of uric acid nephrolithiasis, the hyperuricosuria may require treatment.[15]
Drugs and dietary supplements that may be helpful
- Inositol[citation needed]
- Antiuricosurics
Complications
Although normally benign, idiopathic renal hypouricemia may increase the risk of exercise-induced acute renal failure.[16][17][18]
See also
- Uricosuria (disambiguation)
References
- ^ Chizyński K, Rózycka M (November 2005). "[Hyperuricemia]" (in Polish). Pol. Merkur. Lekarski 19 (113): 693–6. PMID 16498814.
- ^ Ramsdell CM, Kelley WN (February 1973). "The clinical significance of hypouricemia". Annals of internal medicine 78 (2): 239–42. PMID 4683752.
- ^ Garg JP, Chasan-Taber S, Blair A, et al. (January 2005). "Effects of sevelamer and calcium-based phosphate binders on uric acid concentrations in patients undergoing hemodialysis: a randomized clinical trial". Arthritis and rheumatism 52 (1): 290–5. doi:10.1002/art.20781. PMID 15641045.
- ^ Siener R, Hesse A. (2003). "The effect of a vegetarian and different omnivorous diets on urinary risk factors for uric acid stone formation". Eur J Nutr 42 (6): 332–7. doi:10.1007/s00394-003-0428-0. PMID 14673606. http://www.ncbi.nlm.nih.gov/pubmed/14673606.
- ^ a b Szeto YT, Kwok TC, Benzie IF (October 2004). "Effects of a long-term vegetarian diet on biomarkers of antioxidant status and cardiovascular disease risk". Nutrition 20 (10): 863–6. doi:10.1016/j.nut.2004.06.006. PMID 15474873. http://linkinghub.elsevier.com/retrieve/pii/S0899900704001674.
- ^ Koretz RL (November 1981). "Hypouricemia--a transient biochemical phenomenon of total parenteral nutrition". Am. J. Clin. Nutr. 34 (11): 2493–8. PMID 6795918. http://www.ajcn.org/cgi/pmidlookup?view=long&pmid=6795918.
- ^ Moyer RA, John DS (April 2003). "Acute gout precipitated by total parenteral nutrition". J. Rheumatol. 30 (4): 849–50. PMID 12672211.
- ^ Derus CL, Levinson DJ, Bowman B, Bengoa JM, Sitrin MD (October 1987). "Altered fractional excretion of uric acid during total parenteral nutrition". J. Rheumatol. 14 (5): 978–81. PMID 3123676.
- ^ Greene ML, Marcus R, Aurbach GD, Kazam ES, Seegmiller JE (September 1972). "Hypouricemia due to isolated renal tubular defect. Dalmatian dog mutation in man". Am. J. Med. 53 (3): 361–7. doi:10.1016/0002-9343(72)90181-7. PMID 5054729. http://linkinghub.elsevier.com/retrieve/pii/0002-9343(72)90181-7.
- ^ Ichida K, Hosoyamada M, Kamatani N, Kamitsuji S, Hisatome I, Shibasaki T, Hosoya T (September 2008). "Age and origin of the G774A mutation in SLC22A12 causing renal hypouricemia in Japanese". Clin. Genet. 74 (3): 243–51. doi:10.1111/j.1399-0004.2008.01021.x. PMID 18492088. http://www3.interscience.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0009-9163&date=2008&volume=74&issue=3&spage=243.
- ^ Takahashi T, Tsuchida S, Oyamada T, Ohno T, Miyashita M, Saito S, Komatsu K, Takashina K, Takada G (May 2005). "Recurrent URAT1 gene mutations and prevalence of renal hypouricemia in Japanese". Pediatr. Nephrol. 20 (5): 576–8. doi:10.1007/s00467-005-1830-z. PMID 15772829.
- ^ Wakida N, Tuyen DG, Adachi M, Miyoshi T, Nonoguchi H, Oka T, Ueda O, Tazawa M, Kurihara S, Yoneta Y, Shimada H, Oda T, Kikuchi Y, Matsuo H, Hosoyamada M, Endou H, Otagiri M, Tomita K, Kitamura K (April 2005). "Mutations in human urate transporter 1 gene in presecretory reabsorption defect type of familial renal hypouricemia". J. Clin. Endocrinol. Metab. 90 (4): 2169–74. doi:10.1210/jc.2004-1111. PMID 15634722. http://jcem.endojournals.org/cgi/pmidlookup?view=long&pmid=15634722.
- ^ Toncev G, Milicic B, Toncev S, Samardzic G (May 2002). "Serum uric acid levels in multiple sclerosis patients correlate with activity of disease and blood-brain barrier dysfunction". Eur. J. Neurol. 9 (3): 221–6. doi:10.1046/j.1468-1331.2002.00384.x. PMID 11985629. http://www.blackwell-synergy.com/openurl?genre=article&sid=nlm:pubmed&issn=1351-5101&date=2002&volume=9&issue=3&spage=221.
- ^ Crook M (December 1993). "Hypouricaemia in a hospital population". Scand. J. Clin. Lab. Invest. 53 (8): 883–5. doi:10.3109/00365519309086502. PMID 8140400.
- ^ Martín Hernández E, Aparicio López C, Alvarez Calatayud G, García Herrera MA (September 2001). "[Vesical uric acid lithiasis in a child with renal hypouricemia"] (in Spanish; Castilian). An. Esp. Pediatr. 55 (3): 273–6. PMID 11676906. http://db.doyma.es/cgi-bin/wdbcgi.exe/doyma/mrevista.pubmed_full?inctrl=05ZI0103&rev=37&vol=55&num=3&pag=273.
- ^ Ito O, Hasegawa Y, Sato K, Mitsui H, Yuda F, Sato H, Ito S, Kudo K (June 2003). "A case of exercise-induced acute renal failure in a patient with idiopathic renal hypouricemia developed during antihypertensive therapy with losartan and trichlormethiazide" (– Scholar search). Hypertens. Res. 26 (6): 509–13. doi:10.1291/hypres.26.509. PMID 12862209. http://joi.jlc.jst.go.jp/JST.JSTAGE/hypres/26.509?from=PubMed. [dead link]
- ^ Ohta T, Sakano T, Igarashi T, Itami N, Ogawa T (June 2004). "Exercise-induced acute renal failure associated with renal hypouricaemia: results of a questionnaire-based survey in Japan". Nephrol. Dial. Transplant. 19 (6): 1447–53. doi:10.1093/ndt/gfh094. PMID 15150354.
- ^ Mima A, Ichida K, Matsubara T, Kanamori H, Inui E, Tanaka M, Manabe Y, Iehara N, Tanaka Y, Yanagita M, Yoshioka A, Arai H, Kawamura M, Usami K, Hosoya T, Kita T, Fukatsu A (December 2008). "Acute Renal Failure After Exercise in a Japanese Sumo Wrestler With Renal Hypouricemia". Am. J. Med. Sci. 336 (6): 512–514. doi:10.1097/MAJ.0b013e318164717f. PMID 19092327.
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Inborn error of purine-pyrimidine metabolism (E79, 277.2)
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| Purine metabolism |
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Anabolism
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Adenylosuccinate lyase deficiency · Adenosine Monophosphate Deaminase Deficiency type 1
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Nucleotide salvage
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Lesch-Nyhan syndrome/Hyperuricemia · Adenine phosphoribosyltransferase deficiency
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Catabolism
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Adenosine deaminase deficiency · Purine nucleoside phosphorylase deficiency · Xanthinuria · Gout · Mitochondrial neurogastrointestinal encephalopathy syndrome
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| Pyrimidine metabolism |
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Anabolism
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Orotic aciduria · Miller syndrome
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Catabolism
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Dihydropyrimidine dehydrogenase deficiency
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mt, k, c/g/r/p/y/i, f/h/s/l/o/e, a/u, n, m
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k, cgrp/y/i, f/h/s/l/o/e, au, n, m, epon
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m(A16/C10),i(k, c/g/r/p/y/i, f/h/s/o/e, a/u, n, m)
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Abnormal clinical and laboratory findings for blood tests (R70–R79, 790)
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| Red blood cells |
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Size
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Macrocyte · Microcyte · Anisocytosis
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Shape (Poikilocyte)
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membrane abnormalities: Acanthocyte · Codocyte · Ovalocyte · Spherocyte
other: Dacrocyte · Schistocyte · Degmacyte
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Inclusion bodies
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developmental organelles (Howell-Jolly body, Basophilic stippling, Pappenheimer bodies, Cabot rings)
abnormal hemoglobin precipitation (Heinz body)
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Other
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Rouleaux · Reticulocyte · Elevated ESR
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| Lymphocytes |
Smudge cell · Downey cell
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| Small molecules |
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Blood sugar
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Hyperglycemia · Prediabetes (Impaired fasting glucose, Impaired glucose tolerance)
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Nitrogenous
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Azotemia · Hyperuricemia · Hypouricemia
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| Proteins |
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LFT
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Elevated transaminases · Elevated ALP · Hypoproteinemia (Hypoalbuminemia)
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Other
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Elevated cardiac markers · Elevated alpha-fetoprotein
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| Minerals |
Iron overload disorder
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| Pathogens/sepsis |
Bacteremia · Viremia · Fungemia · Parasitemia · Algaemia
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cell/phys (coag, heme, immu, gran), csfs
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rbmg/mogr/tumr/hist, sysi/epon, btst
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drug (B1/2/3+5+6), btst, trns
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noco/acba/cong/tumr, sysi/epon, urte
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proc/itvp, drug (G4B), blte, urte
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