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Regional adiposity and insulin sensitivity—interactions with menopause and HIV in middle-aged black African women

Regional adiposity and insulin sensitivity—interactions with menopause and HIV in middle-aged black African women
Regional adiposity and insulin sensitivity—interactions with menopause and HIV in middle-aged black African women
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, ERα, and PPARγ, 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.
beta-cell function, adipokines, inflammation, estrogen receptors, body composition, tissue biology, subcutaneous adipose tissue
0021-972X
16-29
Masemola, Maphoko
ac19dd6b-c441-4ed9-9093-2f7816deb97a
Mendham, Amy E.
63f08952-baa4-42cc-b472-02462cd3026d
Micklesfield, Lisa K.
e73dd95b-ce79-4dc4-b0be-a8935eb069c8
Pheiffer, Carmen
c68acf9c-b588-4291-9d04-e9bc04aac409
Hawley, James
456633c6-4e8e-40c7-94e2-b8244f6b4996
Kengne, Andre Pascal
1cbc23a3-c104-4f2c-b804-323ce91b856a
Chikowore, Tinashe
b53b1cb9-8363-4e2c-9d62-dc3a8627a7b5
Kufe, Clement Nyuyki
eddc38c9-9992-4726-80c8-4ea6367f0c2d
Crowther, Nigel J.
ca4aa5ba-4f92-4c4d-9736-1dcf303dee40
Norris, Shane
1d346f1b-6d5f-4bca-ac87-7589851b75a4
Storbeck, Karl-Heinz
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Olsson, Tommy
b471ee17-d479-4f76-bd3e-ee88a308de10
Karpe, Fredrik
05abcb32-83b7-44eb-ab12-7c360f4f9c12
Goedecke, Julia H.
27db2aa1-04c2-44e8-9c0e-e9bbe98f2e25
Masemola, Maphoko
ac19dd6b-c441-4ed9-9093-2f7816deb97a
Mendham, Amy E.
63f08952-baa4-42cc-b472-02462cd3026d
Micklesfield, Lisa K.
e73dd95b-ce79-4dc4-b0be-a8935eb069c8
Pheiffer, Carmen
c68acf9c-b588-4291-9d04-e9bc04aac409
Hawley, James
456633c6-4e8e-40c7-94e2-b8244f6b4996
Kengne, Andre Pascal
1cbc23a3-c104-4f2c-b804-323ce91b856a
Chikowore, Tinashe
b53b1cb9-8363-4e2c-9d62-dc3a8627a7b5
Kufe, Clement Nyuyki
eddc38c9-9992-4726-80c8-4ea6367f0c2d
Crowther, Nigel J.
ca4aa5ba-4f92-4c4d-9736-1dcf303dee40
Norris, Shane
1d346f1b-6d5f-4bca-ac87-7589851b75a4
Storbeck, Karl-Heinz
23505057-d47e-4e98-92d3-e0496ceb74f8
Olsson, Tommy
b471ee17-d479-4f76-bd3e-ee88a308de10
Karpe, Fredrik
05abcb32-83b7-44eb-ab12-7c360f4f9c12
Goedecke, Julia H.
27db2aa1-04c2-44e8-9c0e-e9bbe98f2e25

Masemola, Maphoko, Mendham, Amy E., Micklesfield, Lisa K., Pheiffer, Carmen, Hawley, James, Kengne, Andre Pascal, Chikowore, Tinashe, Kufe, Clement Nyuyki, Crowther, Nigel J., Norris, Shane, Storbeck, Karl-Heinz, Olsson, Tommy, Karpe, Fredrik and Goedecke, Julia H. (2024) Regional adiposity and insulin sensitivity—interactions with menopause and HIV in middle-aged black African women. The Journal of Clinical Endocrinology & Metabolism, 110 (1), 16-29. (doi:10.1210/clinem/dgae447).

Record type: Article

Abstract

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, ERα, and PPARγ, 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.

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More information

Submitted date: 14 March 2024
Accepted/In Press date: 27 June 2024
e-pub ahead of print date: 1 July 2024
Published date: 16 July 2024
Keywords: beta-cell function, adipokines, inflammation, estrogen receptors, body composition, tissue biology, subcutaneous adipose tissue

Identifiers

Local EPrints ID: 504787
URI: http://eprints.soton.ac.uk/id/eprint/504787
ISSN: 0021-972X
PURE UUID: 3da537c4-8f0f-415b-9246-3e5244990e5b
ORCID for Shane Norris: ORCID iD orcid.org/0000-0001-7124-3788

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Date deposited: 18 Sep 2025 17:08
Last modified: 19 Sep 2025 02:02

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Contributors

Author: Maphoko Masemola
Author: Amy E. Mendham
Author: Lisa K. Micklesfield
Author: Carmen Pheiffer
Author: James Hawley
Author: Andre Pascal Kengne
Author: Tinashe Chikowore
Author: Clement Nyuyki Kufe
Author: Nigel J. Crowther
Author: Shane Norris ORCID iD
Author: Karl-Heinz Storbeck
Author: Tommy Olsson
Author: Fredrik Karpe
Author: Julia H. Goedecke

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