History and exam

Key diagnostic factors

common

presence of risk factors

Key risk factors include male sex, black race, family history of FSGS, heroin abuse, use of known causative medications, chronic viral infection, a solitary kidney, and obesity.

oedema

Patients may present acutely with overt nephrotic syndrome with oedema. [Figure caption and citation for the preceding image starts]: Facial oedema in a child with nephrotic syndromeFrom the collection of Dr M. Dixit, Medical Director, Florida Children's Kidney Centre; Dr R. Mathias, Chief, Pediatric Nephrology, Nemours Children's Clinic, Orlando, FL [Citation ends].com.bmj.content.model.Caption@cba5fbc

More commonly seen in primary FSGS.

foamy urine

Due to high levels of protein in the urine.

hypertension

Can occur due to increased salt retention and volume overload, or renal dysfunction with decreased glomerular filtration rate.

uncommon

Muehrcke's lines

White banding on the nails due to hypoalbuminaemia. [Figure caption and citation for the preceding image starts]: Muehrcke's lines in a patient with hypoalbuminaemia due to nephrotic syndromeFrom Muehrcke RC. The finger-nails in chronic hypoalbuminaemia: a new physical sign. Br Med J. 1956 Jun 9;1(4979):1327-8 [Citation ends].com.bmj.content.model.Caption@1ab38505

xanthelasma and xanthomata

Cholesterol deposits in the skin due to hypercholesterolaemia. [Figure caption and citation for the preceding image starts]: Xanthomata in a patient with severe hyperlipidaemiaFrom Watkins PJ. Cardiovascular disease, hypertension, and lipids. BMJ. 2003 Apr 19;326(7394):874-6 [Citation ends].com.bmj.content.model.Caption@29802a7a

Other diagnostic factors

common

body mass index 95th percentile or greater

Indicates obesity, a known element in the development of secondary FSGS, probably due to associated pathophysiological factors (e.g., hyperfiltration, insulin resistance) and not just weight per se.[25][32]

uncommon

lymphadenopathy

Generalised lymphadenopathy in HIV patients.

Peripheral lymphadenopathy in patients with systemic lupus erythematosus, which causes non-FSGS nephrotic syndrome.

skin rash

HIV-positive patients may have rashes or post-infective scars, especially shingles.

A photosensitive skin rash may indicate systemic lupus erythematosus, which causes non-FSGS nephrotic syndrome.

oral lesions

Ulcers, angular cheilitis, thrush, oral hairy leukoplakia, oral Kaposi's sarcoma in HIV-positive patients.

nephrectomy scar

A solitary or transplanted kidney is at increased risk of secondary FSGS.

Risk factors

strong

male sex

Males have 1.5- to 2-fold greater risk than females of developing FSGS-induced end-stage renal failure.[16]

black race

A 4- to 7-fold greater risk than white or Asian people of developing FSGS-induced end-stage renal failure.[16] This may be partly explained by mutations in non-muscle myosin heavy chain 9 (MYH9), which are associated with primary and HIV-induced FSGS and are more common in black patients.[19]​Apolipoprotein L1 (APOL1) gene polymorphisms are also associated with FSGS in black patients and appear to be expressed almost exclusively in individuals of African descent.[28][29]

family history of FSGS

Some forms of FSGS are inherited and a positive family history may suggest a genetic cause.

The majority of genetic causes of FSGS in children follow an autosomal recessive pattern with mutations in the genes nephrin (NPHS1), podocin (NPHS2), and phospholipase C epsilon 1( PLCE1) being the most common.[26]​ Autosomal dominant causes of FSGS are more common in adolescents and adults. Major genes implicated in autosomal dominant FSGS include alpha-actinin 4 (ACTN4), inverted formin 2 (INF2), or the transient receptor potential cation 6 channel (TRPC6).[25] MYO1E mutations have been associated with childhood-onset, glucocorticoid-resistant FSGS.​[27]

heroin abuse

Presumed mechanism is a direct toxic effect on the podocyte.

use of known causative medications

Interferon alfa, lithium, sirolimus, and pamidronate.[4] The presumed mechanism is a direct toxic effect on the podocyte.

chronic viral infection

HIV is the most common cause. Rarer causes include persistent parvovirus B19 infection, cytomegalovirus, hepatitis B and C, and SARS-CoV-2.[4]

weak

solitary kidney

Usually due to nephrectomy or congenital.

Produces compensatory glomerular hyperfiltration in the remaining kidney, which predisposes to FSGS.

pre-existing renal disease

Reflux nephropathy and renal dysplasia may cause secondary FSGS.

kidney transplant

Chronic allograft nephropathy can cause secondary FSGS.

acute renal ischaemia

Renal thromboembolism is a rare cause of secondary FSGS.

obesity

A known factor, possibly related to hyperfiltration, insulin resistance leading to increased glomerular capillary wall tension, podocyte stress, growth factors promoting glomerular hypertrophy, and elevated levels of leptin.[25][32]

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