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- Publisher Website: 10.1016/0021-9150(93)90189-2
- Scopus: eid_2-s2.0-0027741436
- PMID: 8141841
- WOS: WOS:A1993MR22600019
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Article: Serum apolipoprotein(a) correlates with growth hormone levels in Chinese patients with acromegaly
Title | Serum apolipoprotein(a) correlates with growth hormone levels in Chinese patients with acromegaly |
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Authors | |
Keywords | acromegaly apolipoprotein(a) growth hormone lipoproteins octreotide |
Issue Date | 1993 |
Publisher | Elsevier Ireland Ltd. The Journal's web site is located at http://www.elsevier.com/locate/atherosclerosis |
Citation | Atherosclerosis, 1993, v. 104 n. 1-2, p. 183-188 How to Cite? |
Abstract | Untreated acromegaly is associated with an increased cardiovascular morbidity and mortality. The contribution of altered lipid metabolism remains unclear. We investigated the relationship between serum apolipoprotein(a) (apo(a)) and growth hormone (GH) levels in 15 patients with acromegaly before and during treatment with octreotide, a long-acting somatostatin analogue, 288-600 μg/day s.c., for 6 months. Before treatment serum apo(a) was significantly elevated in acromegalic patients (geometric mean being 323 U/l vs. 142 U/l in controls (n = 92; P < 0.01)). Octreotide treatment resulted in significant reductions in serum apo(a) concentration (F = 7.22; P < 0.01; geometric mean being 232 U/l and 248 U/l at 3 months and 6 months respectively) and apo(a) concentrations on treatment were not significantly different from control values. There were significant reductions in serum GH (F = 7.30; P < 0.01), insulin growth factor 1 (IGF1) (F = 31.4, P < 0.001) and insulin (F = 4.57; P < 0.05) concentrations. Plasma glycosylated haemoglobin levels were unchanged. Apo(a) levels correlated with serum GH (r = 0.450; P < 0.01) but showed no correlation with basal insulin concentrations. Serum HDL cholesterol increased on treatment (F = 4.29; P < 0.05). Triglycerides were reduced only in the 12 patients without diabetes mellitus (P = 4.75; P < 0.05). No significant change in LDL cholesterol occurred. Our findings suggest that apo(a) may constitute another cardiovascular risk factor in untreated acromegaly and that GH may be involved in the regulation of circulating apo(a) concentration. |
Persistent Identifier | http://hdl.handle.net/10722/162018 |
ISSN | 2023 Impact Factor: 4.9 2023 SCImago Journal Rankings: 1.461 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lam, KSL | en_HK |
dc.contributor.author | Pang, RWC | en_HK |
dc.contributor.author | Janus, ED | en_HK |
dc.contributor.author | Kung, AWC | en_HK |
dc.contributor.author | Wang, CCL | en_HK |
dc.date.accessioned | 2012-09-05T05:16:42Z | - |
dc.date.available | 2012-09-05T05:16:42Z | - |
dc.date.issued | 1993 | en_HK |
dc.identifier.citation | Atherosclerosis, 1993, v. 104 n. 1-2, p. 183-188 | en_HK |
dc.identifier.issn | 0021-9150 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/162018 | - |
dc.description.abstract | Untreated acromegaly is associated with an increased cardiovascular morbidity and mortality. The contribution of altered lipid metabolism remains unclear. We investigated the relationship between serum apolipoprotein(a) (apo(a)) and growth hormone (GH) levels in 15 patients with acromegaly before and during treatment with octreotide, a long-acting somatostatin analogue, 288-600 μg/day s.c., for 6 months. Before treatment serum apo(a) was significantly elevated in acromegalic patients (geometric mean being 323 U/l vs. 142 U/l in controls (n = 92; P < 0.01)). Octreotide treatment resulted in significant reductions in serum apo(a) concentration (F = 7.22; P < 0.01; geometric mean being 232 U/l and 248 U/l at 3 months and 6 months respectively) and apo(a) concentrations on treatment were not significantly different from control values. There were significant reductions in serum GH (F = 7.30; P < 0.01), insulin growth factor 1 (IGF1) (F = 31.4, P < 0.001) and insulin (F = 4.57; P < 0.05) concentrations. Plasma glycosylated haemoglobin levels were unchanged. Apo(a) levels correlated with serum GH (r = 0.450; P < 0.01) but showed no correlation with basal insulin concentrations. Serum HDL cholesterol increased on treatment (F = 4.29; P < 0.05). Triglycerides were reduced only in the 12 patients without diabetes mellitus (P = 4.75; P < 0.05). No significant change in LDL cholesterol occurred. Our findings suggest that apo(a) may constitute another cardiovascular risk factor in untreated acromegaly and that GH may be involved in the regulation of circulating apo(a) concentration. | en_HK |
dc.language | eng | en_US |
dc.publisher | Elsevier Ireland Ltd. The Journal's web site is located at http://www.elsevier.com/locate/atherosclerosis | en_HK |
dc.relation.ispartof | Atherosclerosis | en_HK |
dc.subject | acromegaly | en_HK |
dc.subject | apolipoprotein(a) | en_HK |
dc.subject | growth hormone | en_HK |
dc.subject | lipoproteins | en_HK |
dc.subject | octreotide | en_HK |
dc.subject.mesh | Acromegaly - Blood - Drug Therapy | en_US |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Apolipoproteins A - Analysis | en_US |
dc.subject.mesh | Cholesterol, Hdl - Blood | en_US |
dc.subject.mesh | Cholesterol, Ldl - Blood | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Growth Hormone - Blood | en_US |
dc.subject.mesh | Hemoglobin A, Glycosylated - Analysis | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Insulin - Blood | en_US |
dc.subject.mesh | Insulin-Like Growth Factor I - Analysis | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Octreotide - Therapeutic Use | en_US |
dc.subject.mesh | Prospective Studies | en_US |
dc.subject.mesh | Triglycerides - Blood | en_US |
dc.title | Serum apolipoprotein(a) correlates with growth hormone levels in Chinese patients with acromegaly | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Lam, KSL: ksllam@hku.hk | en_HK |
dc.identifier.email | Pang, RWC: robertap@hkucc.hku.hk | en_HK |
dc.identifier.email | Kung, AWC: awckung@hku.hk | en_HK |
dc.identifier.authority | Lam, KSL=rp00343 | en_HK |
dc.identifier.authority | Pang, RWC=rp00274 | en_HK |
dc.identifier.authority | Kung, AWC=rp00368 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1016/0021-9150(93)90189-2 | - |
dc.identifier.pmid | 8141841 | - |
dc.identifier.scopus | eid_2-s2.0-0027741436 | en_HK |
dc.identifier.volume | 104 | en_HK |
dc.identifier.issue | 1-2 | en_HK |
dc.identifier.spage | 183 | en_HK |
dc.identifier.epage | 188 | en_HK |
dc.identifier.isi | WOS:A1993MR22600019 | - |
dc.publisher.place | Ireland | en_HK |
dc.identifier.scopusauthorid | Lam, KSL=8082870600 | en_HK |
dc.identifier.scopusauthorid | Pang, RWC=7004376659 | en_HK |
dc.identifier.scopusauthorid | Janus, ED=7006936536 | en_HK |
dc.identifier.scopusauthorid | Kung, AWC=7102322339 | en_HK |
dc.identifier.scopusauthorid | Wang, CCL=7501631357 | en_HK |
dc.identifier.issnl | 0021-9150 | - |