Cj. Glueck et al., SEVERE HYPERTRIGLYCERIDEMIA AND PANCREATITIS WHEN ESTROGEN REPLACEMENT THERAPY IS GIVEN TO HYPERTRIGLYCERIDEMIC WOMEN, The Journal of laboratory and clinical medicine, 123(1), 1994, pp. 59-64
Citations number
30
Categorie Soggetti
Medical Laboratory Technology","Medicine, General & Internal
Our specific aim was to assess severe hypertriglyceridemia and pancrea
titis that occurred when postmenopausal estrogen replacement therapy (
ERT) or tamoxifen had been given by their physicians to women with pre
existing, usually covert, primary familial hypertriglyceridemia. We re
trospectively studied 31 women referred for diagnosis and therapy of h
ypertriglyceridemia over 2.75 years whose initial visit fasting plasma
triglyceride levels were >750 mg/dl. Of the 31 women with hypertrigly
ceridemia, 12 (39%) had been given exogenous estrogen by their physici
ans (II ERT, one tamoxifen). Ten of the 12 women, while undergoing ERT
, had triglyceride levels >1200 mg/dl. In triglyceride referral catego
ries 750 to 1000, 1000-1500, and >1500 mg/dl, 17% (2 of 12), 33% (3 of
9), and 70% (7 of 10), respectively, of the 31 women with hypertrigly
ceridemia were receiving ERT. The higher the triglycerides were at ref
erral, the greater was the likelihood that women were taking ERT (X(2)
= 6.6, p = 0.035). Four of the seven women with triglyceride levels >
1500 mg/dl while undergoing ERT were hospitalized with severe acute pa
ncreatitis; another two had severe abdominal pain thought to be pancre
atic in origin. To quickly lower dangerously high triglyceride levels,
ERT was stopped in all 12 women. Lopid (1.2 to 1.5 gm/day) was given
to the seven women not already taking it, and four were also given ome
ga-3 fatty acids (4 to 15 gm/day). Median plasma triglyceride level at
the initial visit in the 12 women undergoing ERT was 1665 mg/dl. At t
heir second visit, approximately 6 weeks later, when not undergoing ER
T, and with all 12 women receiving diet plus Lopid (gemfibrozil), and
with four also taking omega-3 fatty acids, triglyceride levels fell sh
arply to 293 mg/dl (p<0.0005). In women with pre-ERT triglyceride leve
ls >300 mg/dl, ERT is relatively contraindicated and should be absolut
ely contraindicated when triglyceride levels are >750 mg/dl, to avoid
hypertriglyceridemic pancreatitis and exacerbation of preexisting, cov
ert hypertriglyceridemia. Cessation of ERT and treatment with triglyce
ride-lowering regimens usually normalizes triglyceride levels in women
with hypertriglyceridemia, but if ERT is continued, triglyceride-lowe
ring therapy is usually ineffective.