IGF-I, osteocalcin, and bone change in pregnant normotensive and pre-eclamptic women

被引:23
作者
Sowers, M
Scholl, T
Grewal, J
Chen, XH
Jannausch, M
机构
[1] Univ Michigan, Dept Epidemiol, Ann Arbor, MI 48109 USA
[2] Univ Med & Dent New Jersey, Piscataway, NJ 08855 USA
关键词
D O I
10.1210/jc.86.12.5898
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Pre-eclampsia is a pregnancy disorder of uncertain etiology that affects 5-10% of all pregnancies, with symptoms typically presenting around or after 20 wk gestation. We hypothesized that IGF-I, osteocalcin, and bone loss would be different among women with pre-eclampsia compared with normotensive pregnant women. There were 962 pregnant healthy women, aged 12-35, who were assessed at entry to care, at 28 wk, and at delivery for osteocalcin and IGF-I concentrations. Bone ultrasound was measured at entry to care and at 6 wk postpartum, whereas bone mineral density was measured by dual x-ray densitometry at delivery. There were 64 women (6.7%) am ng the women being followed who developed pre-eclampsia. In women with preeclampsia, IGF-I concentrations were 74% greater in the third trimester compared with the first trimester, whereas there was little change in osteocalcin concentrations. In contrast, normotensive women had an average increase of 43% in IGF-I concentrations accompanied by a 63% decline in osteocalcin concentrations. In women with pre-eclampsia, IGF-I and osteocalcin concentrations were significantly correlated (r = 0.48 and 0.43) at both the first and third trimester time points, but only in the third trimester among normotensive women (r = 0.27). The bone change difference between the two groups was not statistically significant. Women with pre-eclampsia appear to have an exaggerated IGF-I responsiveness compared with women who are normotensive; however, the strong correlation between IGF-I and osteocalcin in women with pre-eclampsia suggests that the IGF-I is able to retain its role as a local regulator of bone remodeling, as indicated by the osteocalcin concentrations.
引用
收藏
页码:5898 / 5903
页数:6
相关论文
共 23 条
[1]   Insulin resistance and preeclampsia [J].
Berkowitz, KM .
CLINICS IN PERINATOLOGY, 1998, 25 (04) :873-+
[2]  
BRIXEN K, 1990, J BONE MINER RES, V5, P609
[3]   INSULIN-LIKE GROWTH FACTOR-I MEDIATES SELECTIVE ANABOLIC EFFECTS OF PARATHYROID-HORMONE IN BONE CULTURES [J].
CANALIS, E ;
CENTRELLA, M ;
BURCH, W ;
MCCARTHY, TL .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 83 (01) :60-65
[4]   Insulin-like growth factor-I and bone mineral density [J].
Collins, D ;
Woods, A ;
Herd, R ;
Blake, G ;
Fogelman, I ;
Wheeler, M ;
Swaminathan, R .
BONE, 1998, 23 (01) :13-16
[5]   SHORT-TERM EFFECTS OF RECOMBINANT HUMAN INSULIN-LIKE GROWTH-FACTOR-I ON BONE TURNOVER IN NORMAL WOMEN [J].
EBELING, PR ;
JONES, JD ;
OFALLON, WM ;
JANES, CH ;
RIGGS, BL .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1993, 77 (05) :1384-1387
[6]  
EBELING PR, 1993, J CLIN ENDOCR METAB, V77, P1884
[7]   CIRCULATING LEVELS OF INSULIN-LIKE GROWTH-FACTORS INCREASE AND MOLECULAR-FORMS OF THEIR SERUM BINDING-PROTEINS CHANGE WITH HUMAN-PREGNANCY [J].
GARGOSKY, SE ;
MOYSE, KJ ;
WALTON, PE ;
OWENS, JA ;
WALLACE, JC ;
ROBINSON, JS ;
OWENS, PC .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 170 (03) :1157-1163
[8]   Insulin-like growth factor binding protein-1 at the maternal-fetal interface and insulin-like growth factor-I, insulin-like growth factor-II, and insulin-like growth factor binding protein-1 in the circulation of women with severe preeclampsia [J].
Giudice, LC ;
Martina, NA ;
Crystal, RA ;
Tazuke, S ;
Druzin, M .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1997, 176 (04) :751-757
[9]   Preeclampsia is associated with low circulating levels of insulin-like growth factor I and 1,25-dihydroxyvitamin D in maternal and umbilical cord compartments [J].
Halhali, A ;
Tovar, AR ;
Torres, N ;
Bourges, H ;
Garabedian, M ;
Larrea, F .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (05) :1828-1833
[10]   INSULIN-LIKE GROWTH FACTOR-I HAS INDEPENDENT EFFECTS ON BONE-MATRIX FORMATION AND CELL REPLICATION [J].
HOCK, JM ;
CENTRELLA, M ;
CANALIS, E .
ENDOCRINOLOGY, 1988, 122 (01) :254-260