Shrunken pore syndrome

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Shrunken Pore Syndrome[edit | edit source]

Inner view of fenestrae in capillary of glomerulus

Shrunken Pore Syndrome is a renal condition characterized by a reduction in the size of the glomerular filtration pores, leading to impaired kidney function. This syndrome is associated with a decreased ability of the kidneys to filter small molecules, which can result in various clinical manifestations and complications.

Pathophysiology[edit | edit source]

The primary feature of shrunken pore syndrome is the reduction in the size of the filtration pores within the glomerulus, a network of capillaries located at the beginning of a nephron in the kidney. The glomerulus is responsible for the initial step in the filtration of blood to form urine. In shrunken pore syndrome, the pores through which filtration occurs become smaller, leading to a decreased glomerular filtration rate (GFR).

Diagram of Bowman's capsule and glomerulus

The reduction in pore size affects the kidney's ability to filter small molecules such as creatinine and cystatin C. This can lead to an accumulation of these substances in the blood, which is often used as a marker for kidney function. The syndrome is often identified by a discrepancy between the levels of these markers, with cystatin C levels being disproportionately elevated compared to creatinine levels.

Clinical Significance[edit | edit source]

Shrunken pore syndrome is significant because it can lead to an underestimation of kidney dysfunction if only creatinine levels are used to assess kidney function. This is because the smaller pores preferentially affect the filtration of cystatin C more than creatinine, leading to a misleadingly normal creatinine-based GFR.

Patients with shrunken pore syndrome may present with symptoms of chronic kidney disease, including fatigue, swelling, and changes in urine output. The condition is also associated with an increased risk of cardiovascular disease and mortality.

Diagnosis[edit | edit source]

The diagnosis of shrunken pore syndrome is typically made through the measurement of both creatinine and cystatin C levels in the blood. A significant discrepancy between these two markers, with a higher cystatin C-based GFR compared to creatinine-based GFR, suggests the presence of shrunken pore syndrome.

Management[edit | edit source]

Management of shrunken pore syndrome involves addressing the underlying kidney dysfunction and monitoring for complications. Treatment may include lifestyle modifications, medications to control blood pressure and blood sugar levels, and interventions to reduce cardiovascular risk.

Related Pages[edit | edit source]

Diagram illustrating shrunken pore syndrome

See Also[edit | edit source]

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Contributors: Prab R. Tumpati, MD