PMID- 1701370 OWN - NLM STAT- MEDLINE DCOM- 19910124 LR - 20190813 IS - 0300-0664 (Print) IS - 0300-0664 (Linking) VI - 33 IP - 3 DP - 1990 Sep TI - Decreased sex hormone binding globulin (SHBG) and insulin-like growth factor binding protein (IGFBP-1) in extreme obesity. PG - 415-22 AB - Obesity may be characterized by abnormal sex steroid secretion and reduced sex hormone binding globulin (SHBG) which in turn is related to fat distribution and insulin secretion. Recent in-vitro and in-vivo evidence suggests that insulin is the common mechanism regulating the secretion of SHBG and insulin-like growth factor small binding protein (IGFBP-1). IGFBP-1 appears not only to be a carrier for insulin growth factors (IGFs) but also to play an active role in growth processes, independent of growth hormone secretion. We have examined the possible relationship between fasting insulin, SHBG, testosterone, IGF-1, IGFBP-1 and fat distribution in 25 extremely obese, menstruating women (mean weight 107 +/- 3 kg) with normal glucose tolerance. Fat distribution was assessed from measurements of the waist to hip ratio (W/H). The obese women showed an elevated fasting insulin (mean +/- SEM; 21 +/- 2 mumol/l), a normal IGF-1, but reduced IGFBP-1 (14.6 +/- 2 micrograms/l); in 15 women IGFBP-1 levels were undetectable by the present assay. In addition, SHBG levels were reduced in the obese women (24 +/- 2 nmol/l) but total testosterone values (1.9 +/- 0.1 nmol/l) were normal. The elevated fasting insulin levels were positively correlated with increasing upper segment obesity as expressed by a rising W/H ratio (P less than 0.01, r2 = 0.306) and inversely correlated with SHBG (P less than 0.01, r2 = 0.483). Similarly, reduced SHBG values showed an inverse correlation with increasing W/H ratio (P less than 0.001, r2 = 0.383). No correlation was found between IGFBP-1 and W/H ratio but a strong positive correlation was seen between IGFBP-1 and SHBG (P less than 0.001, r2 = 0.466). Furthermore, an equally significant inverse correlation was found between IGFBP-1 and insulin levels (P less than 0.001, r2 = 0.474).(ABSTRACT TRUNCATED AT 250 WORDS) FAU - Weaver, J U AU - Weaver JU AD - Medical Unit, London Hospital, UK. FAU - Holly, J M AU - Holly JM FAU - Kopelman, P G AU - Kopelman PG FAU - Noonan, K AU - Noonan K FAU - Giadom, C G AU - Giadom CG FAU - White, N AU - White N FAU - Virdee, S AU - Virdee S FAU - Wass, J A AU - Wass JA LA - eng PT - Journal Article PL - England TA - Clin Endocrinol (Oxf) JT - Clinical endocrinology JID - 0346653 RN - 0 (Carrier Proteins) RN - 0 (Insulin) RN - 0 (Insulin-Like Growth Factor Binding Proteins) RN - 0 (Sex Hormone-Binding Globulin) RN - 0 (Somatomedins) RN - 3XMK78S47O (Testosterone) RN - 67763-96-6 (Insulin-Like Growth Factor I) SB - IM MH - Adipose Tissue/metabolism MH - Adult MH - Carrier Proteins/*blood MH - Female MH - Humans MH - Insulin/blood/*physiology MH - Insulin-Like Growth Factor Binding Proteins MH - Insulin-Like Growth Factor I/analysis MH - Obesity/*blood MH - Sex Hormone-Binding Globulin/*metabolism MH - Somatomedins/*analysis MH - Testosterone/blood EDAT- 1990/09/01 00:00 MHDA- 1990/09/01 00:01 CRDT- 1990/09/01 00:00 PHST- 1990/09/01 00:00 [pubmed] PHST- 1990/09/01 00:01 [medline] PHST- 1990/09/01 00:00 [entrez] AID - 10.1111/j.1365-2265.1990.tb00507.x [doi] PST - ppublish SO - Clin Endocrinol (Oxf). 1990 Sep;33(3):415-22. doi: 10.1111/j.1365-2265.1990.tb00507.x.