Background. Lupus nephritis is one of the most serious complications in pat
ients with systemic lupus erythematosus (SLE). Both immunological and nonim
munological factors are known to be involved in the progression of this typ
e of glomerulopathy. The present study was designed to clarify the clinicop
athological significance of ACE (angiotensin converting enzyme) gene polymo
rphism in patients with lupus nephritis.
Methods. Genomic DNA was obtained from 25 biopsy-proven Japanese lupus neph
ritis patients. Insertion/deletion (ID) polymorphism of the ACE gene was de
termined using PCR (polymerase chain reaction). Association between ACE gen
e polymorphism and clinicopathological factors was evaluated in a cross-sec
tional study.
Results. The frequency of insertion/insertion (II)! ID and deletion/deletio
n (DD) in ACE genotypes was 44, 52, and 4%, respectively. Patients were div
ided into two groups according to the presence or absence of D allele, name
ly II and ID + DD. Serum ACE activities were significantly higher in the ID
+ DD group than in the II group (12.7 +/- 3.2 vs. 7.83 +/- 1.9 IU/l, p = 0
.002). There was no difference between the two groups in terms of associati
on with hypertension, or decreased renal function. ACE genotypes were not a
ssociated with the degree of proteinuria or incidence of nephrotic syndrome
. The frequency of the World Health Organization (WHO) class IV renal lesio
n, which is the most severe form of nephritis, was not associated with ACE
genotype.
Conclusions. These findings suggest that the D allele of the ACE gene may b
e related to higher levels of serum ACE activity in lupus nephritis, althou
gh its clinical significance still remains to be determined.