Ub. Berg et al., KIDNEY MORPHOLOGICAL-CHANGES IN RELATION TO LONG-TERM RENAL-FUNCTION AND METABOLIC CONTROL IN ADOLESCENTS WITH IDDM, Diabetologia, 41(9), 1998, pp. 1047-1056
For the past 10-15 years all the children at our unit with insulin-dep
endent diabetes mellitus have been repeatedly followed-up with renal f
unction tests. Renal biopsy, examined by light and electron microscopy
, was included in the follow-up of 36 adolescents and young adults, ag
ed 13-25 years, with a disease duration of 7-19 years. All subjects ha
d undergone at least three renal function tests before biopsy and none
had persistent microalbuminuria. Renal function was evaluated as glom
erular filtration rate and effective renal plasma flow determined by c
learances of inulin and para-amino hippuric acid. Glomerular filtratio
n rate and filtration fraction were increased before and at the time o
f the biopsy. Glomerular basement membrane thickness (331-858 nm) and
mesangial matrix volume fraction (7.4-17.1%) were increased. Long-term
hyperfiltration and hyperperfusion before biopsy correlated inversely
with mean glomerular volume. Increased filtration fraction before the
biopsy correlated directly with mean of all HbA(1c) (r = 0.485, p < 0
.01) and both variables correlated directly with mesangial matrix volu
me fraction, basement membrane thickness and structural index (r = 0.4
33, p < 0.01 and r = 0.626, p < 0.001, respectively). Urinary albumin
excretion rate correlated directly with foot process width (r = 0.645,
p < 0.001). By multiple regression analysis the most important variab
le for the increase in basal membrane thickness was the metabolic cont
rol while the mean of previous filtration fraction was most important
for the increase in mesangial matrix volume. In conclusion, although n
one of the patients showed constant microalbuminuria, early diabetic s
tructural changes were evident with basal membrane thickening and incr
eased mesangial matrix volume. The structural changes related to long-
standing hyperfiltration and poor metabolic control.