History and exam

Key diagnostic factors

common

edema

Typically generalized, including the lower extremities and periorbital regions.

elevated BP

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

Other diagnostic factors

common

incidental proteinuria or abnormal renal function

Patients may present after being referred with the incidental finding of proteinuria or abnormal renal function.

xanthelasma

Commonly seen owing to resulting hypercholesterolemia.

foamy urine

May be caused by increased protein in the urine.

uncommon

fatigue/malaise

Nonspecific symptom that may indicate an underlying secondary cause.

anorexia

Nonspecific symptom that may indicate an underlying secondary cause.

Muehrcke lines

White lines of the nails due to hypoalbuminemia.

Risk factors

strong

male sex

Male to female ratio is 2:1.[4]​ ​​

age >40 years

Primary MN is more common after 40 years of age.[2]​ The mean age at diagnosis is between 50 to 60 years.[4]​ ​​

HLA-DR3

Associated with a higher risk of MN.[11]

autoimmune disease

About 10% to 20% of patients with lupus nephritis have MN.​[12]​ Sjogren syndrome, rheumatoid arthritis, and mixed connective tissue disease are examples of other autoimmune diseases that are associated with secondary MN.​​​[1]

hepatitis B and C

Circulating antigen-antibody complexes can deposit in the subepithelial space, leading to MN. These infections can also lead to membranoproliferative glomerulonephritis.[13]​​[14]​​

syphilis

Now a rare cause, but circulating antigen-antibody complexes can be deposited in the subepithelial space, leading to MN.

solid organ carcinoma

Lung and colorectal (most common) carcinomas may lead to tumor antigen deposition on the subepithelial surface and complement activation.​[15]​​

medications

Uses of nonsteroidal anti-inflammatory drugs (NSAIDs), gold, penicillamine, lithium, and captopril have been implicated as causes.​​​[1][16]​​ The mechanism associated with drug-induced MN is not clear. Proteinuria generally develops within the first 6 to 12 months of drug treatment but can occur as late as 3 to 4 years. Discontinuation of the drug leads to resolution of the proteinuria in virtually all cases.​​​​​​​​​

weak

sarcoidosis

In one study, MN was the most frequent glomerular disease occurring in sarcoidosis.[17]​​​

postrenal transplantation

Both recurrent and de novo MN have been reported after renal transplantation.​[18]​​​

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