Microalbuminuria is a term to describe a moderate increase in the level of urine albumin. It occurs when the kidney leaks small amounts of albumin into the urine, in other words, when an abnormally high permeability for albumin in the glomerulus of the kidney occurs. Normally, the kidneys filter albumin, so if albumin is found in the urine, then it is a marker of kidney disease. The term microalbuminuria is now discouraged by Kidney Disease Improving Global Outcomes[1] and has been replaced by moderately increased albuminuria.

Quick Facts Other names, Specialty ...
Microalbuminuria
Other namesModerately Increased Albuminuria
SpecialtyNephrology
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Causes

Higher dietary intake of animal protein, animal fat, and cholesterol may increase risk for microalbuminuria,[2] and generally, diets higher in fruits, vegetables, and whole grains but lower in meat and sweets may be protective against kidney function decline.[3][4][5]

Associations

Microalbuminuria is an important adverse predictor of glycemic outcomes in prediabetes. Prediabetes individuals with increased microalbuminuria even in the so-called normal range is associated with increased progression to diabetes and decreased reversal to normoglycemia. Hence, prediabetes individuals with microalbuminuria warrant more aggressive intervention to prevent diabetes in them.[7]

Diagnosis and treatment

The level of albumin protein produced by microalbuminuria can be detected by special albumin-specific urine dipsticks, which have a lower detection threshold than standard urine dipsticks. A microalbumin urine test determines the presence of the albumin in urine. In a properly functioning body, albumin is not normally present in urine because it is retained in the bloodstream by the kidneys.

Microalbuminuria can be diagnosed from a 24-hour urine collection (between 30 and 300 mg/24 hours) or, more commonly, from elevated concentration in a spot sample (30 to 300 mg/L). Both must be measured on at least two of three measurements over a two- to three-month period.[8]

An albumin level above the upper limit values is called "macroalbuminuria", or sometimes just albuminuria. Sometimes, the upper limit value is given as one less (such as 300 being given as 299) to mark that the higher value (here 300) is defined as macroalbuminuria.[9]

Taurine in combination with N-acetylcysteine (Nefrosave Tablet) was useful in attenuating UACR in microalbuminuric type 2 diabetic patient as per Indian Journal of Nephrology 2008

To compensate for variations in urine concentration in spot-check samples, comparing the amount of albumin in the sample against its concentration of creatinine is helpful. This is termed the albumin/creatinine ratio (ACR)[10] and microalbuminuria is defined as ACR ≥3.5 mg/mmol (female) or ≥2.5 mg/mmol (male),[11] or with both substances measured by mass, as an ACR between 30 and 300 μg albumin/mg creatinine.[12] For the diagnosis of microalbuminuria, care must be taken when collecting sample for the urine ACR. An early-morning sample is preferred. The patient should refrain from heavy exercises 24 hours before the test. A repeat test should be done 3 to 6 months after the first positive test for microalbuminuria. Lastly, the test is inaccurate in a person with very high or very low muscle mass. This is due to the variation in creatinine level which is produced by the muscle.[13]

More information Individual, Lower limit ...
Definitions of microalbuminuria
IndividualLower limitUpper limitUnit
24h urine collection 30[9]300[9]mg/24h (milligram albumin per 24 hours)
Short-time urine collection 20[9]200[9]μg/min (microgram albumin per minute)
Spot urine albumin sample 30[14]300[14]mg/L (milligram albumin per liter of urine)
Spot urine albumin/creatinine ratio Women3.5[15]25[15] or 35[15]mg/mmol (milligram albumin per millimole creatinine)
30[15]400[15]μg/mg (microgram albumin per milligram creatinine)
Men2.5[15] or 3.5[15]25[15] or 35[15]mg/mmol
30[15]300[15]μg/mg
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References

  • Abid O, Sun Q, Sugimoto K, Mercan D, Vincent JL (2001). "Predictive value of microalbuminuria in medical ICU patients: results of a pilot study". Chest. 120 (6): 1984–8. doi:10.1378/chest.120.6.1984. PMID 11742932.
  • Andersen S, Blouch K, Bialek J, Deckert M, Parving HH, Myers BD (2000). "Glomerular permselectivity in early stages of overt diabetic nephropathy". Kidney Int. 58 (5): 2129–37. doi:10.1111/j.1523-1755.2000.00386.x. PMID 11044234.
  • Heart Outcomes Prevention Evaluation Study Investigators (2000). "Effects of ramipril on cardiovascular and microvascular outcomes in people with diabetes mellitus: results of the HOPE study and MICRO-HOPE substudy". Lancet. 355 (9200): 253–9. doi:10.1016/S0140-6736(99)12323-7. PMID 10675071. S2CID 1863533.
  • Lemley KV, Abdullah I, Myers BD, et al. (2000). "Evolution of incipient nephropathy in type 2 diabetes mellitus". Kidney Int. 58 (3): 1228–37. doi:10.1046/j.1523-1755.2000.00223.x. PMID 10972685.
  • Lièvre M, Marre M, Chatellier G, et al. (2000). "The non-insulin-dependent diabetes, hypertension, microalbuminuria or proteinuria, cardiovascular events, and ramipril (DIABHYCAR) study: design, organization, and patient recruitment. DIABHYCAR Study Group". Controlled Clinical Trials. 21 (4): 383–96. doi:10.1016/S0197-2456(00)00060-X. PMID 10913814.
  • Parving HH, Lehnert H, Bröchner-Mortensen J, Gomis R, Andersen S, Arner P (2001). "The effect of irbesartan on the development of diabetic nephropathy in patients with type 2 diabetes". N. Engl. J. Med. 345 (12): 870–8. doi:10.1056/NEJMoa011489. PMID 11565519.
  • Kidney Disease: Improving Global Outcomes (KDIGO) CKD Work Group. KDIGO 2012 Clinical Practice Guideline for the Evaluation and Management of Chronic Kidney Disease. Kidney inter., Suppl. 2013; 3: 1–150.

Footnotes

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