Regional Adiposity and Insulin Sensitivity-Interactions With Menopause and HIV in Middle-Aged Black African Women

被引:1
作者
Masemola, Maphoko [1 ]
Mendham, Amy E. [1 ,2 ,3 ]
Micklesfield, Lisa K. [1 ]
Pheiffer, Carmen [4 ,5 ,6 ]
Hawley, James [7 ]
Kengne, Andre Pascal [8 ]
Chikowore, Tinashe [1 ]
Kufe, Clement Nyuyki [1 ,9 ]
Crowther, Nigel J. [10 ,11 ]
Norris, Shane [1 ]
Storbeck, Karl-Heinz [12 ]
Olsson, Tommy [13 ]
Karpe, Fredrik [14 ,15 ]
Goedecke, Julia H. [1 ,4 ]
机构
[1] Univ Witwatersrand, Fac Hlth Sci, South African Med Res Council, WITS Dev Pathways Hlth Res Unit DPHRU,Dept Paedia, Johannesburg, South Africa
[2] South Australia Hlth, Riverland Acad Clin Excellence, Riverland Mallee Coorong Local Hlth Network, Berri, SA 5343, Australia
[3] Univ Cape Town, Hlth Phys Act Lifestyle & Sport Res Ctr HPALS, FIMS Int Collaborating Ctr Sports Med, Dept Human Biol,Fac Hlth Sci,Div Physiol Sci, ZA-7700 Cape Town, South Africa
[4] South African Med Res Council, Biomed Res & Innovat Platform, ZA-7505 Cape Town, South Africa
[5] Stellenbosch Univ, Fac Med & Hlth Sci, Ctr Cardiometab Res Afr CARMA, Div Med Physiol, ZA-7505 Cape Town, South Africa
[6] Univ Pretoria, Fac Hlth Sci, Dept Obstet & Gynaecol, ZA-0002 Pretoria, South Africa
[7] Univ Manchester, NHS Fdn Trust, Dept Biochem, Manchester M13 9WL, England
[8] South African Med Res Council, Noncommunicable Dis Res Unit, ZA-7505 Cape Town, South Africa
[9] Univ Witwatersrand, Fac Hlth Sci, Sch Clin Med, Dept Anaesthesiol, ZA-2050 Johannesburg, South Africa
[10] Natl Hlth Lab Serv, Dept Chem Pathol, ZA-2192 Johannesburg, South Africa
[11] Univ Witwatersrand, Fac Hlth Sci, ZA-2192 Johannesburg, South Africa
[12] Stellenbosch Univ, Dept Biochem, ZA-7600 Stellenbosch, South Africa
[13] Umea Univ, Dept Publ Hlth & Clin Med, S-90187 Umea, Sweden
[14] Univ Oxford, Oxford Ctr Diabet Endocrinol & Metab, Oxford OX3 7LE, England
[15] Oxford Univ Hosp Trust, Natl Inst Hlth Res, Oxford Biomed Res Ctr, Oxford OX3 7LE, England
基金
英国医学研究理事会; 新加坡国家研究基金会;
关键词
beta-cell function; adipokines; inflammation; estrogen receptors; body composition; tissue biology; subcutaneous adipose tissue; HORMONE-BINDING GLOBULIN; ESTROGEN-RECEPTOR-ALPHA; ANTIRETROVIRAL THERAPY; TISSUE; OBESITY; RESISTANCE; INFLAMMATION; EXPRESSION; BETA; FAT;
D O I
10.1210/clinem/dgae447
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective To explore depot-specific functional aspects of adipose tissue, examining the putative role for menopause and HIV status on insulin sensitivity (SI) and beta-cell function in Black South African women. Methods Women (n = 92) from the Middle-Aged Soweto Cohort, including premenopausal HIV-negative women (n = 21); premenopausal women living with HIV (LWH; n = 11); postmenopausal HIV-negative women (n = 42); and postmenopausal women LWH (n = 18) underwent the following tests: body composition (dual-energy x-ray absorptiometry); fasting bloods for sex hormones, inflammation, and adipokines; frequently sampled intravenous glucose tolerance test for SI and beta-cell function (disposition index, DI); abdominal (aSAT) and gluteal subcutaneous adipose tissue (gSAT) biopsies for cell size, and mRNA expression of adipokines, inflammation, and estrogen receptors (ER). Results Depot-specific associations between gene expression and insulin parameters did not differ by HIV or menopause status. Pooled analysis showed significant models for SI (P = .002) and DI (P = .003). Higher SI was associated with lower leptin and CD11c expression in aSAT and higher adiponectin in gSAT. Higher DI was associated with higher aSAT and gSAT expression of adiponectin, lipoprotein lipase, ER alpha, and PPAR gamma, and lower leptin in aSAT. Women LWH had higher expression of adiponectin and lower expression of leptin in both aSAT (P = .002 and P = .005) and gSAT (P = .004 and P = .002), respectively, and a larger proportion of smaller cells in aSAT (P < .001). Conclusion Insulin sensitivity and beta-cell function were distinctively associated with aSAT and gSAT. While menopause did not influence these relationships, HIV had a significant effect on adipose tissue, characterized by variations in cell size distribution and transcript levels within the depots.
引用
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页码:16 / 29
页数:14
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