Glycosuria: Difference between revisions
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==Overview== | ==Overview== | ||
'''Glycosuria''' or '''glucosuria''' is an abnormal condition of [[osmotic]] [[diuresis]] due to excretion of [[glucose]] by the kidneys. | '''Glycosuria''' or '''glucosuria''' is an abnormal condition of [[osmotic]] [[diuresis]] due to excretion of [[glucose]] by the kidneys. The most common cause of glycosuria is untreated [[diabetes mellitus]]. The condition occurs when [[blood plasma|plasma]] glucose levels rise above kidney threshold for glucose reabsorption. At this point, the excess plasma glucose will not be reabsorbed in the proximal tubule and is excreted in the urine. When the excess glucose is excreted in the urine, it makes water enter the urine due to high osmolarity of the urine. This leads to the characteristic symptom of high urine volumes. Glycosuria can be either a physiologic response of the body to elevated blood glucose levels, such as alimentary glycosuria; or it can be a pathologic phenomenon. When glycosuria occurs at normal plasma glucose concentrations due to decreased renal threshold for glucose reabsorption, it is reffered to as [[renal glycosuria]]. Glycosuria has been targeted as a therapeutic option for diseases such as diabetes mellitus, as induction of glycosuria leads to better glycemic control and decreases risk of [[cardiovascular diseases]] in diabetic patients. | ||
==Causes== | |||
== | ==== Conditions ==== | ||
'''Drugs Causing Glycosuria''' | * [[Diabetes mellitus]] | ||
* Pregnancy | |||
'''Drugs Causing Glycosuria<ref name=":1" />''' | |||
*[[Chlorpromazine]] | *[[Chlorpromazine]] | ||
*[[Cidofovir]] | *[[Cidofovir]] | ||
Line 31: | Line 31: | ||
*[[Prednisolone]] | *[[Prednisolone]] | ||
*[[Streptozocin]] | *[[Streptozocin]] | ||
*[[ACE inhibitor|ACE]] Inhibitors ([[Captopril]], [[Enalapril]]) | |||
*[[SGLT2]] Inhibitors | |||
'''Other chemicals causing glycosuria''' | |||
* [[Ethanol]] | |||
* [[Arsenic]] | |||
==Historical Perspective== | ==Historical Perspective== | ||
* | *Glycosuria was first discovered by von Mering and Minkowski in 1889. | ||
==Classification== | ==Classification== | ||
:Glycosuria can be classified into the following groups, based on the etiology of glucose excretion in urine: | |||
:* | :*Alimentary glycosuria | ||
:* | :*Renal Glycosuria | ||
:* | :*Diabetic glycosuria | ||
* | :*Iatrogenic glycosuria | ||
:*Glycosuria as part of a syndrome or disease (e.g. [[Fanconi syndrome]] or [[Wilson disease]]) | |||
==Pathophysiology== | ==Pathophysiology== | ||
*The pathogenesis of | *The pathogenesis of glycosuria is characterized by either increased [[Blood sugar|plasma glucose]] or decreased proximal tubule threshold for glucose excretion. | ||
* | *Genetic mutations can contribute to pathogenesis in glycosuria, especially renal glycosuria, these mutations include: [[SLC5A2]] and [[HNF1A]]<ref name=":1">{{Cite web|url=https://academic.oup.com/jcem/article/102/5/1548/2954944|title=Clinical and Genetic Features of Patients With Type 2 Diabetes and Renal Glycosuria|last=|first=|date=|website=|archive-url=|archive-date=|dead-url=|access-date=}}</ref>. | ||
* | *When plasma glucose levels exceed 180 mg/mL, the excess glucose will not be reabsorbed and is excreted in urine. However, proximal tubule threshold for glucose reabsorbtion varies among individuals and in difference stages of one's life span. | ||
* | |||
==Clinical Features== | |||
Simultaneous excretion of glucose and water into urine leads to: | |||
* [[Polyuria]] | |||
* [[polydipsia]] | |||
==Differentiating Glycosuria from other Diseases== | |||
*When excessive amounts of glucose is found in urine, the following diagnoses should be in mind: | |||
:*Diabetes Mellitus | |||
:*Renal glycosuria | |||
:*Alimentary glycosuria | |||
:*[[Fanconi syndrome]] (presence of glucose as well as other solutes in urine) | |||
:*[[Wilson disease]] | |||
Different causes of glycosuria can be differentiated based on: | |||
== | {| style="border: 0px; font-size: 90%; margin: 3px;" align="center" | ||
! rowspan="2" style="background: #4479BA; text-align: center;" |{{fontcolor|#FFF|Disease}} | |||
! colspan="5" style="background: #4479BA; text-align: center;" |{{fontcolor|#FFF|History and symptoms}} | |||
! colspan="8" style="background: #4479BA; text-align: center;" |{{fontcolor|#FFF|Laboratory findings}} | |||
! rowspan="2" style="background: #4479BA; text-align: center;" |{{fontcolor|#FFF|Additional findings}} | |||
|- | |||
! style="background: #4479BA; text-align: center;" |{{fontcolor|#FFF|Polyuria}} | |||
! style="background: #4479BA; text-align: center;" |{{fontcolor|#FFF|Polydipsia}} | |||
! style="background: #4479BA; text-align: center;" |{{fontcolor|#FFF|Polyphagia}} | |||
! style="background: #4479BA; text-align: center;" |{{fontcolor|#FFF|="center" style="background:#DCDCDC;"|Weight loss}} | |||
! style="background: #4479BA; text-align: center;" |{{fontcolor|#FFF|Weight gain}} | |||
! style="background: #4479BA; text-align: center;" |{{fontcolor|#FFF|Serum glucose}} | |||
! style="background: #4479BA; text-align: center;" |{{fontcolor|#FFF|Urinary Glucose}} | |||
! style="background: #4479BA; text-align: center;" |{{fontcolor|#FFF|Urine PH}} | |||
! style="background: #4479BA; text-align: center;" |{{fontcolor|#FFF|Serum Sodium}} | |||
! style="background: #4479BA; text-align: center;" |{{fontcolor|#FFF|Urinary Glucose}} | |||
! style="background: #4479BA; text-align: center;" |{{fontcolor|#FFF|24 hrs cortisol level}} | |||
! style="background: #4479BA; text-align: center;" |{{fontcolor|#FFF|C-peptide level}} | |||
! style="background: #4479BA; text-align: center;" |{{fontcolor|#FFF|Serum glucagon}} | |||
|- | |||
| style="padding: 5px 5px; background: #DCDCDC;" align="center" |[[Diabetes mellitus type 1|Type 1 Diabetes mellitus]] | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | + | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | + | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | + | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | + | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | - | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |'''↑''' | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |'''''↑''''' | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |N/'''↑''' | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |'''↓''' | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Auto antibodies present | |||
([[GAD65|Anti GAD-65]] and anti insulin anti bodies) | |||
|- | |||
| style="padding: 5px 5px; background: #DCDCDC;" align="center" |[[Diabetes mellitus type 2|Type 2 Diabetes mellitus]] | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | + | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | + | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | + | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | + | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | - | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |'''↑''' | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |'''↑''' | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |'''↑''' | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |'''↑''' | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |[[Acanthosis nigricans]] | |||
|- | |||
| style="padding: 5px 5px; background: #DCDCDC;" align="center" |[[MODY]] | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | + | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | + | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | + | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | - | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | + | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |'''↑''' | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |'''↑''' | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |'''↑''' | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |N | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | - | |||
|- | |||
| style="padding: 5px 5px; background: #DCDCDC;" align="center" |Transient [[hyperglycemia]] | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | - | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | - | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | - | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | - | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | - | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |'''↑''' | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |'''↑''' | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |'''↑''' | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |N/'''↑''' | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |In hospitalized patients especially in [[ICU]] and [[CCU]] | |||
|- | |||
| style="padding: 5px 5px; background: #DCDCDC;" align="center" |[[Steroid]] therapy | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | + | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | - | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | - | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | - | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | + | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |'''↑''' | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |'''↑''' | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |'''↑''' | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |'''↑''' | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |N/'''↑''' | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |N/'''↑''' | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |[[Acanthosis nigricans|Acanthosis nigricans,]] | |||
|- | |||
| style="padding: 5px 5px; background: #DCDCDC;" align="center" |[[RTA|RTA 1]] | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | - | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | - | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | - | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | + | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | - | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |'''↑''' | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |'''↑''' | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |[[Hypokalemia]], [[nephrolithiasis]] | |||
|- | |||
| style="padding: 5px 5px; background: #DCDCDC;" align="center" |[[Glucagonoma]] | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | - | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | - | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | - | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | - | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | - | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |'''↑''' | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | - | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |'''↑''' | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |[[Necrolytic migratory erythema]] | |||
|- | |||
| style="padding: 5px 5px; background: #DCDCDC;" align="center" |[[Cushing's syndrome|Cushing syndrome]] | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | - | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | - | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | - | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | - | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | + | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |'''↑''' | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" | - | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |'''↓''' | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |N/'''↑''' | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |'''↑''' | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |Normal | |||
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |[[Moon face]], [[obesity]], [[buffalo hump]], easy [[Bruising|bruisibility]] | |||
|} | |||
==Epidemiology and Demographics== | ==Epidemiology and Demographics== | ||
* The prevalence of | * The prevalence of glycosuria in general population is approximately 3000-5000 per 100,000 individuals worldwide<ref>{{Cite web|url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1958671/|title=Prevalence of Glycosuria and Diabetes Mellitus|last=|first=|date=|website=|archive-url=|archive-date=|dead-url=|access-date=}}</ref>. | ||
* | * Prevalence of glycosuria is increasing due to: | ||
** Increased incidence of DM. | |||
** Increased use of medications such as SGLT2 inhibitors (in order to decreased blood glucose levels to reach a better glycemic control). | |||
===Age=== | ===Age=== | ||
*Patients of all age groups may develop | *Patients of all age groups may develop glycosuria. | ||
*As the patients' age increases, glycosuria increases due to decreased kidney threshold for glucose reabsorption<ref name=":2">{{Cite web|url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1749121/|title=Renal glucose threshold variations with age|last=|first=|date=|website=|archive-url=|archive-date=|dead-url=|access-date=}}</ref>. | |||
===Gender=== | ===Gender=== | ||
* | *Glycosuria affects both men and women. | ||
*Glycosuria is more common among males<ref name=":2" />. | |||
===Race=== | ===Race=== | ||
* | *The incidence of glycosuria varies among different nationalities, however; there is no propensity to a specific race. | ||
==Risk Factors== | ==Risk Factors== | ||
* | *SLC5A2 mutation causes familial renal glycosuria<ref>{{Cite web|url=https://www.ncbi.nlm.nih.gov/pubmed/14569097|title=Molecular analysis of the SGLT2 gene in patients with renal glucosuria.|last=|first=|date=|website=|archive-url=|archive-date=|dead-url=|access-date=}}</ref> | ||
*Diabetes mellitus | |||
*Exposure to medications or chemicals causing glycosuria. | |||
== Natural History, Complications and Prognosis== | == Natural History, Complications and Prognosis== | ||
*Early clinical features include polyuria, polydipsia, [[hypoglycemia]] and weight loss due to excretion of glucose as a source of energy. | |||
*Early clinical features include | *Common complications of glycosuria include polyuria, polydipsia, and mild growth retardation. | ||
*Glycosuria increases as the patients age due to decreased renal threshold for glucose excretion<ref name=":0">{{Cite web|url=https://www.ncbi.nlm.nih.gov/pubmed/5141588|title=The prevalence and causes of glycosuria in 28,765 young men in the population in Singapore.|last=|first=|date=|website=|archive-url=|archive-date=|dead-url=|access-date=}}</ref>. | |||
*Common complications of | *Prognosis is generally excellent. There are no reports of mortality directly attributed to glycosuria. | ||
* | |||
== Diagnosis == | == Diagnosis == | ||
===Diagnostic Criteria=== | ===Diagnostic Criteria=== | ||
Diagnosis of glycosuria depends on the type of glycosuria: | |||
:* | |||
:* | For renal glycosuria<ref name=":0" />: | ||
* Glycosuria in the face of normal blood glucose levels, normal glycosylated hemoglobin and normal free fatty acids | |||
:* | * Glycosuria independent of carbohydrate consumption | ||
* No diabetic symptoms | |||
For Alimentary glycosuria<ref name=":0" />: | |||
* Normal fasting blood sugar | |||
* Normal 2-hours post-prandial blood glucose | |||
* Maximum blood glucose levels exceeding 180 mg/mL | |||
Diabetic glycosuria: | |||
* Glycosuria in the setting of known diabeties mellitus | |||
: | |||
=== Symptoms === | === Symptoms === | ||
*Symptoms of glycosuriamay include the following: | |||
*Symptoms of | :*Polyuria | ||
:* | :*Polydipsia | ||
:*Weight loss | |||
:* | |||
:* | |||
=== Physical Examination === | === Physical Examination === | ||
Patients with glycosuria generally appear normal in physical examination. | |||
In specific conditions, such as pregnancy or starvation, patients may: | |||
* Appear dehydrated | |||
* Have ketosis | |||
=== Laboratory Findings === | === Laboratory Findings === | ||
* | *Presence of glucose in urine sample. | ||
*Blood sugar may or may not be elevated epending on the pathophysiology and the cause of glycosuria. | |||
*Beside glucose, other solutes can be found in urine, depending on the pathophysiology and the cause of glycosuria. | |||
=== Other Diagnostic Studies === | === Other Diagnostic Studies === | ||
* | *Microscopic urine analysis. | ||
* | *Urine sample test for presence of glucose using [[glucose oxidase]] reagent strips. | ||
== Treatment == | == Treatment == | ||
=== Medical Therapy === | === Medical Therapy === | ||
* | *Tight glycemic control in cases of diabetes mellitus. | ||
=== Prevention === | === Prevention === | ||
*There are no primary preventive measures available for | *There are no primary preventive measures available for glycosuria except for that of glycemic control. | ||
* | *Diet high in protein can lower the proportion of glucose in diet and reduce glucose excretion in urine<ref>{{Cite web|url=https://www.nejm.org/doi/full/10.1056/NEJM192002121820702|title=Diet Reduction with Retention of Protein to Relieve Glycosuria in Diabetes Mellitus|last=|first=|date=|website=|archive-url=|archive-date=|dead-url=|access-date=}}</ref>. | ||
==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2 | ||
}} | |||
<references /> | |||
==See also== | ==See also== | ||
* [[Renal glycosuria]] | * [[Renal glycosuria]] | ||
{{Abnormal clinical and laboratory findings}} | {{Abnormal clinical and laboratory findings}} | ||
[[Category:Diabetes]] | [[Category:Diabetes]] |
Latest revision as of 21:36, 24 January 2019
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Glycosuria or glucosuria is an abnormal condition of osmotic diuresis due to excretion of glucose by the kidneys. The most common cause of glycosuria is untreated diabetes mellitus. The condition occurs when plasma glucose levels rise above kidney threshold for glucose reabsorption. At this point, the excess plasma glucose will not be reabsorbed in the proximal tubule and is excreted in the urine. When the excess glucose is excreted in the urine, it makes water enter the urine due to high osmolarity of the urine. This leads to the characteristic symptom of high urine volumes. Glycosuria can be either a physiologic response of the body to elevated blood glucose levels, such as alimentary glycosuria; or it can be a pathologic phenomenon. When glycosuria occurs at normal plasma glucose concentrations due to decreased renal threshold for glucose reabsorption, it is reffered to as renal glycosuria. Glycosuria has been targeted as a therapeutic option for diseases such as diabetes mellitus, as induction of glycosuria leads to better glycemic control and decreases risk of cardiovascular diseases in diabetic patients.
Causes
Conditions
- Diabetes mellitus
- Pregnancy
Drugs Causing Glycosuria[1]
- Chlorpromazine
- Cidofovir
- Hydrochlorothiazide
- Prednisolone
- Streptozocin
- ACE Inhibitors (Captopril, Enalapril)
- SGLT2 Inhibitors
Other chemicals causing glycosuria
Historical Perspective
- Glycosuria was first discovered by von Mering and Minkowski in 1889.
Classification
- Glycosuria can be classified into the following groups, based on the etiology of glucose excretion in urine:
- Alimentary glycosuria
- Renal Glycosuria
- Diabetic glycosuria
- Iatrogenic glycosuria
- Glycosuria as part of a syndrome or disease (e.g. Fanconi syndrome or Wilson disease)
Pathophysiology
- The pathogenesis of glycosuria is characterized by either increased plasma glucose or decreased proximal tubule threshold for glucose excretion.
- Genetic mutations can contribute to pathogenesis in glycosuria, especially renal glycosuria, these mutations include: SLC5A2 and HNF1A[1].
- When plasma glucose levels exceed 180 mg/mL, the excess glucose will not be reabsorbed and is excreted in urine. However, proximal tubule threshold for glucose reabsorbtion varies among individuals and in difference stages of one's life span.
Clinical Features
Simultaneous excretion of glucose and water into urine leads to:
Differentiating Glycosuria from other Diseases
- When excessive amounts of glucose is found in urine, the following diagnoses should be in mind:
- Diabetes Mellitus
- Renal glycosuria
- Alimentary glycosuria
- Fanconi syndrome (presence of glucose as well as other solutes in urine)
- Wilson disease
Different causes of glycosuria can be differentiated based on:
Disease | History and symptoms | Laboratory findings | Additional findings | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Polyuria | Polydipsia | Polyphagia | Weight loss | Weight gain | Serum glucose | Urinary Glucose | Urine PH | Serum Sodium | Urinary Glucose | 24 hrs cortisol level | C-peptide level | Serum glucagon | ||
Type 1 Diabetes mellitus | + | + | + | + | - | ↑ | ↑ | Normal | Normal | N/↑ | Normal | ↓ | Normal | Auto antibodies present
(Anti GAD-65 and anti insulin anti bodies) |
Type 2 Diabetes mellitus | + | + | + | + | - | ↑ | ↑ | Normal | Normal | ↑ | Normal | Normal | ↑ | Acanthosis nigricans |
MODY | + | + | + | - | + | ↑ | ↑ | Normal | Normal | ↑ | Normal | Normal | N | - |
Transient hyperglycemia | - | - | - | - | - | ↑ | ↑ | Normal | Normal | ↑ | Normal | Normal | N/↑ | In hospitalized patients especially in ICU and CCU |
Steroid therapy | + | - | - | - | + | ↑ | ↑ | Normal | Normal | ↑ | ↑ | N/↑ | N/↑ | Acanthosis nigricans, |
RTA 1 | - | - | - | + | - | Normal | Normal | ↑ | Normal | ↑ | Normal | Normal | Normal | Hypokalemia, nephrolithiasis |
Glucagonoma | - | - | - | - | - | ↑ | Normal | Normal | Normal | - | Normal | Normal | ↑ | Necrolytic migratory erythema |
Cushing syndrome | - | - | - | - | + | ↑ | - | Normal | ↓ | N/↑ | ↑ | Normal | Normal | Moon face, obesity, buffalo hump, easy bruisibility |
Epidemiology and Demographics
- The prevalence of glycosuria in general population is approximately 3000-5000 per 100,000 individuals worldwide[2].
- Prevalence of glycosuria is increasing due to:
- Increased incidence of DM.
- Increased use of medications such as SGLT2 inhibitors (in order to decreased blood glucose levels to reach a better glycemic control).
Age
- Patients of all age groups may develop glycosuria.
- As the patients' age increases, glycosuria increases due to decreased kidney threshold for glucose reabsorption[3].
Gender
- Glycosuria affects both men and women.
- Glycosuria is more common among males[3].
Race
- The incidence of glycosuria varies among different nationalities, however; there is no propensity to a specific race.
Risk Factors
- SLC5A2 mutation causes familial renal glycosuria[4]
- Diabetes mellitus
- Exposure to medications or chemicals causing glycosuria.
Natural History, Complications and Prognosis
- Early clinical features include polyuria, polydipsia, hypoglycemia and weight loss due to excretion of glucose as a source of energy.
- Common complications of glycosuria include polyuria, polydipsia, and mild growth retardation.
- Glycosuria increases as the patients age due to decreased renal threshold for glucose excretion[5].
- Prognosis is generally excellent. There are no reports of mortality directly attributed to glycosuria.
Diagnosis
Diagnostic Criteria
Diagnosis of glycosuria depends on the type of glycosuria:
For renal glycosuria[5]:
- Glycosuria in the face of normal blood glucose levels, normal glycosylated hemoglobin and normal free fatty acids
- Glycosuria independent of carbohydrate consumption
- No diabetic symptoms
For Alimentary glycosuria[5]:
- Normal fasting blood sugar
- Normal 2-hours post-prandial blood glucose
- Maximum blood glucose levels exceeding 180 mg/mL
Diabetic glycosuria:
- Glycosuria in the setting of known diabeties mellitus
Symptoms
- Symptoms of glycosuriamay include the following:
- Polyuria
- Polydipsia
- Weight loss
Physical Examination
Patients with glycosuria generally appear normal in physical examination.
In specific conditions, such as pregnancy or starvation, patients may:
- Appear dehydrated
- Have ketosis
Laboratory Findings
- Presence of glucose in urine sample.
- Blood sugar may or may not be elevated epending on the pathophysiology and the cause of glycosuria.
- Beside glucose, other solutes can be found in urine, depending on the pathophysiology and the cause of glycosuria.
Other Diagnostic Studies
- Microscopic urine analysis.
- Urine sample test for presence of glucose using glucose oxidase reagent strips.
Treatment
Medical Therapy
- Tight glycemic control in cases of diabetes mellitus.
Prevention
- There are no primary preventive measures available for glycosuria except for that of glycemic control.
- Diet high in protein can lower the proportion of glucose in diet and reduce glucose excretion in urine[6].
References
- ↑ 1.0 1.1 "Clinical and Genetic Features of Patients With Type 2 Diabetes and Renal Glycosuria".
- ↑ "Prevalence of Glycosuria and Diabetes Mellitus".
- ↑ 3.0 3.1 "Renal glucose threshold variations with age".
- ↑ "Molecular analysis of the SGLT2 gene in patients with renal glucosuria".
- ↑ 5.0 5.1 5.2 "The prevalence and causes of glycosuria in 28,765 young men in the population in Singapore".
- ↑ "Diet Reduction with Retention of Protein to Relieve Glycosuria in Diabetes Mellitus".
See also
Template:Abnormal clinical and laboratory findings