Obesity, Body Image Dissatisfaction, and Sexual Dysfunction: A Narrative Review
Abstract
:1. Introduction
2. Methods
3. The Pathophysiology of Obesity
3.1. Obesity and Adipose Tissue Dysregulation
3.2. Obesity and Systemic Inflammation
3.3. Obesity and Metabolic Inflexibility
4. Obesity and Sexual Dysfunction
5. Obesity, Social Stereotypes, and Body Image Dissatisfaction
6. The Human Sexual Response Cycle
7. The Interplay of Obesity, Body Image Dissatisfaction, and Sexual Functioning
8. Alternative Perspectives on Obesity: Body Positivity and Size Acceptance
9. Discussion and Conclusions
9.1. Interpretation of Results
9.2. Limitations
9.3. Implications for Future Research and Practice
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Acknowledgments
Conflicts of Interest
Appendix A
Section/Topic in Manuscript | References Cited | Number of References |
---|---|---|
Introduction: Prevalence, Economic, and Health Consequences of Obesity | [1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20] | n = 20 |
Methods of the Literature Review | [21,22,23] | n = 3 |
Pathophysiological Mechanisms of Obesity and Lifestyle Interventions | [24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59] | n = 36 |
Obesity and Sexual Dysfunction | [24,29,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77] | n = 20 |
Obesity, Social Stigma, Body Image, and Bariatric Surgery | [78,79,80,81,82,83,84,85,86,87,88,89,90,91,92,93,94,95,96,97,98,99,100,101,102] | n = 25 |
The Human Sexual Response Cycle | [103,104,105,106,107,108,109,110,111,112,113,114,115,116,117] | n = 15 |
Interplay of Obesity, Body Image, and Sexual Dysfunction | [118,119,120,121,122] | n = 5 |
Body Positivity and Size Acceptance | [123,124,125,126,127,128,129,130,131,132,133,134,135] | n = 13 |
Discussion and Conclusions | [121,136,137,138,139,140,141] | n = 7 |
References
- Hales, C.M.; Fryar, C.D.; Carroll, M.D.; Freedman, D.S.; Ogden, C.L. Trends in Obesity and Severe Obesity Prevalence in US Youth and Adults by Sex and Age, 2007–2008 to 2015–2016. JAMA 2018, 319, 1723–1725. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Hales, C.M.; Carroll, M.D.; Fryar, C.D.; Ogden, C.L. Prevalence of Obesity and Severe Obesity Among Adults: United States, 2017–2018. NCHS Data Brief 2020, 360, 1–8. [Google Scholar]
- Fryar, C.D.; Carroll, M.D.; Afful, J. Prevalence of Overweight, Obesity, and Severe Obesity among Adults Aged 20 and over: United States, 1960–1962 through 2017–2018. National Center for Health Statistics, 2020. Available online: https://www.cdc.gov/nchs/data/hestat/obesity-adult-17-18/overweight-obesity-adults-H.pdf (accessed on 5 January 2022).
- Finkelstein, E.A.; Khavjou, O.A.; Thompson, H.; Trogdon, J.G.; Pan, L.; Sherry, B.; Dietz, W. Obesity and Severe Obesity Forecasts Through 2030. Am. J. Prev. Med. 2012, 42, 563–570. [Google Scholar] [CrossRef] [PubMed]
- Chooi, Y.C.; Ding, C.; Magkos, F. The epidemiology of obesity. Metabolism 2019, 92, 6–10. [Google Scholar] [CrossRef] [Green Version]
- Withrow, D.; Alter, D.A. The economic burden of obesity worldwide: A systematic review of the direct costs of obesity. Obes. Rev. 2011, 12, 131–141. [Google Scholar] [CrossRef]
- Min, J.; Zhao, Y.; Slivka, L.; Wang, Y. Double burden of diseases worldwide: Coexistence of undernutrition and overnutrition-related non-communicable chronic diseases. Obes. Rev. 2018, 19, 49–61. [Google Scholar] [CrossRef]
- Drewnowski, A. Obesity, diets, and social inequalities. Nutr. Rev. 2009, 67 (Suppl. 1), S36–S39. [Google Scholar] [CrossRef]
- Ogden, C.L.; Fryar, C.D.; Hales, C.M.; Carroll, M.D.; Aoki, Y.; Freedman, D.S. Differences in Obesity Prevalence by Demographics and Urbanization in US Children and Adolescents, 2013–2016. JAMA 2018, 319, 2410–2418. [Google Scholar] [CrossRef]
- Janssen, I.; Katzmarzyk, P.T.; Boyce, W.F.; Vereecken, C.; Mulvihill, C.; Roberts, C.; Currie, C.; Pickett, W. Comparison of overweight and obesity prevalence in school-aged youth from 34 countries and their relationships with physical activity and dietary patterns. Obes. Rev. 2005, 6, 123–132. [Google Scholar] [CrossRef]
- Singh, A.S.; Mulder, C.; Twisk, J.W.; van Mechelen, W.; Chinapaw, M.J. Tracking of childhood overweight into adulthood: A systematic review of the literature. Obes. Rev. 2008, 9, 474–488. [Google Scholar] [CrossRef]
- Linder, B.L.; Fradkin, J.E.; Rodgers, G.P. The TODAY Study: An NIH Perspective on Its Implications for Research. Diabetes Care 2013, 36, 1775. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- TODAY Study Group. Effects of Metformin, Metformin Plus Rosiglitazone, and Metformin Plus Lifestyle on Insulin Sensitivity and β-Cell Function in TODAY. Diabetes Care 2013, 36, 1749. [Google Scholar] [CrossRef] [Green Version]
- Esfahani, S.B.; Pal, S. Does Metabolic Syndrome Impair Sexual Functioning in Adults With Overweight and Obesity? Int. J. Sex. Health 2019, 31, 170–185. [Google Scholar] [CrossRef]
- Kim, D.; Hou, W.; Wang, F.; Arcan, C. Factors Affecting Obesity and Waist Circumference Among US Adults. Prev. Chronic Dis. 2019, 16, E02. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Abdullah, A.; Peeters, A.; de Courten, M.; Stoelwinder, J. The magnitude of association between overweight and obesity and the risk of diabetes: A meta-analysis of prospective cohort studies. Diabetes Res. Clin. Pract. 2010, 89, 309–319. [Google Scholar] [CrossRef] [PubMed]
- Patel, S.A.; Deepa, M.; Shivashankar, R.; Ali, M.K.; Kapoor, D.; Gupta, R.; Lall, D.; Tandon, N.; Mohan, V.; Kadir, M.M.; et al. Comparison of multiple obesity indices for cardiovascular disease risk classification in South Asian adults: The CARRS Study. PLoS ONE 2017, 12, e0174251. [Google Scholar] [CrossRef] [Green Version]
- Maiorino, M.I.; Bellastella, G.; Giugliano, D.; Esposito, K. From inflammation to sexual dysfunctions: A journey through diabetes, obesity, and metabolic syndrome. J. Endocrinol. Investig. 2018, 41, 1249–1258. [Google Scholar] [CrossRef]
- Esposito, K.; Giugliano, F.; Ciotola, M.; De Sio, M.; D’Armiento, M.; Giugliano, D. Obesity and sexual dysfunction, male and female. Int. J. Impot. Res. 2008, 20, 358–365. [Google Scholar] [CrossRef] [Green Version]
- Larsen, S.H.; Wagner, G.; Heitmann, B.L. Sexual function and obesity. Int. J. Obes. 2007, 31, 1189–1198. [Google Scholar] [CrossRef] [Green Version]
- Rosen, R.; Brown, C.; Heiman, J.; Leiblum, S.; Meston, C.; Shabsigh, R.; Ferguson, D.; D’Agostino, R., Jr. The Female Sexual Function Index (FSFI): A multidimensional self-report instrument for the assessment of female sexual function. J. Sex Marital Ther. 2000, 26, 191–208. [Google Scholar] [CrossRef] [PubMed]
- Wiegel, M.; Meston, C.; Rosen, R. The female sexual function index (FSFI): Cross-validation and development of clinical cutoff scores. J. Sex Marital Ther. 2005, 31, 1–20. [Google Scholar] [CrossRef]
- Rosen, R.C.; Riley, A.; Wagner, G.; Osterloh, I.H.; Kirkpatrick, J.; Mishra, A. The international index of erectile function (IIEF): A multidimensional scale for assessment of erectile dysfunction. Urology 1997, 49, 822–830. [Google Scholar] [CrossRef] [Green Version]
- Rowland, D.L.; McNabney, S.M.; Mann, A.R. Sexual Function, Obesity, and Weight Loss in Men and Women. Sex. Med. Rev. 2017, 5, 323–338. [Google Scholar] [CrossRef] [PubMed]
- Harvey, I.; Boudreau, A.; Stephens, J.M. Adipose tissue in health and disease. Open Biol. 2020, 10, 200291. [Google Scholar] [CrossRef] [PubMed]
- Da Silva Rosa, S.C.; Nayak, N.; Caymo, A.M.; Gordon, J.W. Mechanisms of muscle insulin resistance and the cross-talk with liver and adipose tissue. Physiol. Rep. 2020, 8, e14607. [Google Scholar] [CrossRef] [PubMed]
- Petersen, M.C.; Shulman, G.I. Mechanisms of Insulin Action and Insulin Resistance. Physiol. Rev. 2018, 98, 2133–2223. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Samuel, V.T.; Shulman, G.I. The pathogenesis of insulin resistance: Integrating signaling pathways and substrate flux. J. Clin. Investig. 2016, 126, 12–22. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Frayn, K.N. Metabolic Regulation: A Human Perspective, 3rd ed.; Wiley-Blackwell: Malden, MA, USA, 2010. [Google Scholar]
- Coen, P.M.; Goodpaster, B.H. Role of intramyocelluar lipids in human health. Trends Endocrinol. Metab. 2012, 23, 391–398. [Google Scholar] [CrossRef] [Green Version]
- Goodpaster, B.H.; Sparks, L.M. Metabolic Flexibility in Health and Disease. Cell Metab. 2017, 25, 1027–1036. [Google Scholar] [CrossRef] [Green Version]
- Muoio, D.M. Metabolic inflexibility: When mitochondrial indecision leads to metabolic gridlock. Cell 2014, 159, 1253–1262. [Google Scholar] [CrossRef] [Green Version]
- Sangwung, P.; Petersen, K.F.; Shulman, G.I.; Knowles, J.W. Mitochondrial Dysfunction, Insulin Resistance, and Potential Genetic Implications. Endocrinology 2020, 161, bqaa017. [Google Scholar] [CrossRef] [PubMed]
- Bäck, M.; Yurdagul, A., Jr.; Tabas, I.; Öörni, K.; Kovanen, P.T. Inflammation and its resolution in atherosclerosis: Mediators and therapeutic opportunities. Nat. Rev. Cardiol. 2019, 16, 389–406. [Google Scholar] [CrossRef] [PubMed]
- Netea, M.G.; Balkwill, F.; Chonchol, M.; Cominelli, F.; Donath, M.Y.; Giamarellos-Bourboulis, E.J.; Golenbock, D.; Gresnigt, M.S.; Heneka, M.T.; Hoffman, H.M.; et al. A guiding map for inflammation. Nat. Immunol. 2017, 18, 826–831. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Poznyak, A.; Grechko, A.V.; Poggio, P.; Myasoedova, V.A.; Alfieri, V.; Orekhov, A.N. The Diabetes Mellitus-Atherosclerosis Connection: The Role of Lipid and Glucose Metabolism and Chronic Inflammation. Int. J. Mol. Sci. 2020, 21, 1835. [Google Scholar] [CrossRef] [Green Version]
- Floyd, Z.E.; Stephens, J.M. Controlling a master switch of adipocyte development and insulin sensitivity: Covalent modifications of PPARγ. Biochim. Biophys. Acta 2012, 1822, 1090–1095. [Google Scholar] [CrossRef] [Green Version]
- Cao, Y. Adipose tissue angiogenesis as a therapeutic target for obesity and metabolic diseases. Nat. Rev. Drug Discov. 2010, 9, 107–115. [Google Scholar] [CrossRef]
- Murano, I.; Barbatelli, G.; Parisani, V.; Latini, C.; Muzzonigro, G.; Castellucci, M.; Cinti, S. Dead adipocytes, detected as crown-like structures, are prevalent in visceral fat depots of genetically obese mice. J. Lipid Res. 2008, 49, 1562–1568. [Google Scholar] [CrossRef] [Green Version]
- Altintas, M.M.; Azad, A.; Nayer, B.; Contreras, G.; Zaias, J.; Faul, C.; Reiser, J.; Nayer, A. Mast cells, macrophages, and crown-like structures distinguish subcutaneous from visceral fat in mice. J. Lipid Res. 2011, 52, 480–488. [Google Scholar] [CrossRef] [Green Version]
- Lin, D.; Chun, T.H.; Kang, L. Adipose extracellular matrix remodelling in obesity and insulin resistance. Biochem. Pharmacol. 2016, 119, 8–16. [Google Scholar] [CrossRef] [Green Version]
- Kenđel Jovanović, G.; Mrakovcic-Sutic, I.; Pavičić Žeželj, S.; Šuša, B.; Rahelić, D.; Klobučar Majanović, S. The Efficacy of an Energy-Restricted Anti-Inflammatory Diet for the Management of Obesity in Younger Adults. Nutrients 2020, 12, 3583. [Google Scholar] [CrossRef]
- Ruiz-Canela, M.; Zazpe, I.; Shivappa, N.; Hébert, J.R.; Sánchez-Tainta, A.; Corella, D.; Salas-Salvadó, J.; Fitó, M.; Lamuela-Raventós, R.M.; Rekondo, J.; et al. Dietary inflammatory index and anthropometric measures of obesity in a population sample at high cardiovascular risk from the PREDIMED (PREvención con DIeta MEDiterránea) trial. Br. J. Nutr. 2015, 113, 984–995. [Google Scholar] [CrossRef] [Green Version]
- Fuentes, G.C.; Castañer, O.; Warnberg, J.; Subirana, I.; Buil-Cosiales, P.; Salas-Salvadó, J.; Corella, D.; Serra-Majem, L.; Romaguera, D.; Estruch, R.; et al. Prospective association of physical activity and inflammatory biomarkers in older adults from the PREDIMED-Plus study with overweight or obesity and metabolic syndrome. Clin. Nutr. 2020, 39, 3092–3098. [Google Scholar] [CrossRef] [PubMed]
- McLeod, A.; Schiffer, L.; Castellanos, K.; DeMott, A.; Olender, S.; Fitzgibbon, M.; Hughes, S.; Fantuzzi, G.; Tussing-Humphreys, L. Impact of Physical Activity and Weight Loss on Fat Mass, Glucose Metabolism, and Inflammation in Older African Americans with Osteoarthritis. Nutrients 2020, 12, 3299. [Google Scholar] [CrossRef] [PubMed]
- Hasson, R.E.; Adam, T.C.; Davis, J.N.; Kelly, L.A.; Ventura, E.E.; Byrd-Williams, C.E.; Toledo-Corral, C.M.; Roberts, C.K.; Lane, C.J.; Azen, S.P.; et al. Randomized controlled trial to improve adiposity, inflammation, and insulin resistance in obese African-American and Latino youth. Obesity 2012, 20, 811–818. [Google Scholar] [CrossRef]
- Lee, S.; Libman, I.; Hughan, K.; Kuk, J.L.; Jeong, J.H.; Zhang, D.; Arslanian, S. Effects of Exercise Modality on Insulin Resistance and Ectopic Fat in Adolescents with Overweight and Obesity: A Randomized Clinical Trial. J. Pediatr. 2019, 206, 91–98.e91. [Google Scholar] [CrossRef]
- Freitas, W.R., Jr.; Oliveira, L.V.F.; Perez, E.A.; Ilias, E.J.; Lottenberg, C.P.; Silva, A.S.; Urbano, J.J.; Oliveira, M.C., Jr.; Vieira, R.P.; Ribeiro-Alves, M.; et al. Systemic Inflammation in Severe Obese Patients Undergoing Surgery for Obesity and Weight-Related Diseases. Obes. Surg. 2018, 28, 1931–1942. [Google Scholar] [CrossRef] [Green Version]
- Devarshi, P.P.; McNabney, S.M.; Henagan, T.M. Skeletal Muscle Nucleo-Mitochondrial Crosstalk in Obesity and Type 2 Diabetes. Int. J. Mol. Sci. 2017, 18, 831. [Google Scholar] [CrossRef] [Green Version]
- Koves, T.R.; Ussher, J.R.; Noland, R.C.; Slentz, D.; Mosedale, M.; Ilkayeva, O.; Bain, J.; Stevens, R.; Dyck, J.R.; Newgard, C.B.; et al. Mitochondrial overload and incomplete fatty acid oxidation contribute to skeletal muscle insulin resistance. Cell Metab. 2008, 7, 45–56. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Ruegsegger, G.N.; Creo, A.L.; Cortes, T.M.; Dasari, S.; Nair, K.S. Altered mitochondrial function in insulin-deficient and insulin-resistant states. J. Clin. Investig. 2018, 128, 3671–3681. [Google Scholar] [CrossRef] [Green Version]
- Townsend, L.K.; Brunetta, H.S.; Mori, M.A.S. Mitochondria-associated ER membranes in glucose homeostasis and insulin resistance. Am. J. Physiol. Endocrinol. Metab. 2020, 319, E1053–E1060. [Google Scholar] [CrossRef]
- Gao, Z.; Yin, J.; Zhang, J.; Ward, R.E.; Martin, R.J.; Lefevre, M.; Cefalu, W.T.; Ye, J. Butyrate Improves Insulin Sensitivity and Increases Energy Expenditure in Mice. Diabetes 2009, 58, 1509. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Vidrine, K.; Ye, J.; Martin, R.J.; McCutcheon, K.L.; Raggio, A.M.; Pelkman, C.; Durham, H.A.; Zhou, J.; Senevirathne, R.N.; Williams, C.; et al. Resistant starch from high amylose maize (HAM-RS2) and dietary butyrate reduce abdominal fat by a different apparent mechanism. Obesity 2014, 22, 344–348. [Google Scholar] [CrossRef]
- McNabney, S.M.; Henagan, T.M. Short Chain Fatty Acids in the Colon and Peripheral Tissues: A Focus on Butyrate, Colon Cancer, Obesity and Insulin Resistance. Nutrients 2017, 9, 1348. [Google Scholar] [CrossRef] [Green Version]
- Robertson, M.D.; Wright, J.W.; Loizon, E.; Debard, C.; Vidal, H.; Shojaee-Moradie, F.; Russell-Jones, D.; Umpleby, A.M. Insulin-sensitizing effects on muscle and adipose tissue after dietary fiber intake in men and women with metabolic syndrome. J. Clin. Endocrinol. Metab. 2012, 97, 3326–3332. [Google Scholar] [CrossRef] [Green Version]
- Mukaida, S.; Evans, B.A.; Bengtsson, T.; Hutchinson, D.S.; Sato, M. Adrenoceptors promote glucose uptake into adipocytes and muscle by an insulin-independent signaling pathway involving mechanistic target of rapamycin complex 2. Pharmacol. Res. 2017, 116, 87–92. [Google Scholar] [CrossRef] [PubMed]
- Krishnapuram, R.; Kirk-Ballard, H.; Dhurandhar, E.J.; Dubuisson, O.; Messier, V.; Rabasa-Lhoret, R.; Hegde, V.; Aggarwal, S.; Dhurandhar, N.V. Insulin receptor-independent upregulation of cellular glucose uptake. Int. J. Obes. 2013, 37, 146–153. [Google Scholar] [CrossRef] [Green Version]
- Di Meo, S.; Iossa, S.; Venditti, P. Improvement of obesity-linked skeletal muscle insulin resistance by strength and endurance training. J. Endocrinol. 2017, 234, R159–R181. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Badoud, F.; Lam, K.P.; Perreault, M.; Zulyniak, M.A.; Britz-McKibbin, P.; Mutch, D.M. Metabolomics Reveals Metabolically Healthy and Unhealthy Obese Individuals Differ in their Response to a Caloric Challenge. PLoS ONE 2015, 10, e0134613. [Google Scholar] [CrossRef] [Green Version]
- Mongraw-Chaffin, M.; Foster, M.C.; Kalyani, R.R.; Vaidya, D.; Burke, G.L.; Woodward, M.; Anderson, C.A.M. Obesity Severity and Duration Are Associated With Incident Metabolic Syndrome: Evidence Against Metabolically Healthy Obesity From the Multi-Ethnic Study of Atherosclerosis. J. Clin. Endocrinol. Metab. 2016, 101, 4117–4124. [Google Scholar] [CrossRef]
- Torres, J.M.; Cox, N.J.; Philipson, L.H. Genome wide association studies for diabetes: Perspective on results and challenges. Pediatr. Diabetes 2013, 14, 90–96. [Google Scholar] [CrossRef] [PubMed]
- Kronenberg, F. Genome-wide association studies in aging-related processes such as diabetes mellitus, atherosclerosis and cancer. Exp. Gerontol. 2008, 43, 39–43. [Google Scholar] [CrossRef]
- Langenberg, C.; Lotta, L.A. Genomic insights into the causes of type 2 diabetes. Lancet 2018, 391, 2463–2474. [Google Scholar] [CrossRef]
- Zahid, H.; Simpson, E.R.; Brown, K.A. Inflammation, dysregulated metabolism and aromatase in obesity and breast cancer. Curr. Opin. Pharmacol. 2016, 31, 90–96. [Google Scholar] [CrossRef]
- Bhardwaj, P.; Au, C.C.; Benito-Martin, A.; Ladumor, H.; Oshchepkova, S.; Moges, R.; Brown, K.A. Estrogens and breast cancer: Mechanisms involved in obesity-related development, growth and progression. J. Steroid Biochem. Mol. Biol. 2019, 189, 161–170. [Google Scholar] [CrossRef] [PubMed]
- Kim, S.O.; Lee, H.S.; Ahn, K.; Park, K. Effect of estrogen deprivation on the expression of aquaporins and nitric oxide synthases in rat vagina. J. Sex. Med. 2009, 6, 1579–1586. [Google Scholar] [CrossRef]
- Benetti-Pinto, C.L.; Ferreira, S.R.; Antunes, A., Jr.; Yela, D.A. The influence of body weight on sexual function and quality of life in women with polycystic ovary syndrome. Arch. Gynecol. Obstet. 2015, 291, 451–455. [Google Scholar] [CrossRef] [PubMed]
- Cushman, T.T.; Kim, N.; Hoyt, R.; Traish, A.M. Estradiol ameliorates diabetes-induced changes in vaginal structure of db/db mouse model. J. Sex. Med. 2009, 6, 2467–2479. [Google Scholar] [CrossRef]
- Lee, H.S.; Li, Z.; Kim, S.O.; Ahn, K.; Kim, N.N.; Park, K. Effect of hyperglycemia on expression of aquaporins in the rat vagina. Urology 2012, 80, 737.e7. [Google Scholar] [CrossRef]
- Pei, L.; Jiang, J.; Jiang, R.; Ouyang, F.; Yang, H.; Cheng, Y.; Fan, Z. Expression of aquaporin proteins in vagina of diabetes mellitus rats. J. Sex. Med. 2013, 10, 342–349. [Google Scholar] [CrossRef]
- Bijlsma-Rutte, A.; Braamse, A.M.J.; van Oppen, P.; Snoek, F.J.; Enzlin, P.; Leusink, P.; Nijpels, G.; Elders, P.J.M. Screening for sexual dissatisfaction among people with type 2 diabetes in primary care. J. Diabetes Complicat. 2017, 31, 1614–1619. [Google Scholar] [CrossRef]
- Pei, L.; Yang, G.; Jiang, J.; Jiang, R.; Deng, Q.; Chen, B.; Gan, X. Expression of aquaporins in prostate and seminal vesicles of diabetic rats. J. Sex. Med. 2013, 10, 2975–2985. [Google Scholar] [CrossRef] [PubMed]
- Corbin, J.D.; Francis, S.H. Cyclic GMP phosphodiesterase-5: Target of sildenafil. J. Biol. Chem. 1999, 274, 13729–13732. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Allahdadi, K.J.; Hannan, J.L.; Tostes, R.C.; Webb, R.C. Endothelin-1 induces contraction of female rat internal pudendal and clitoral arteries through ET(A) receptor and rho-kinase activation. J. Sex. Med. 2010, 7, 2096–2103. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Allahdadi, K.J.; Hannan, J.L.; Ergul, A.; Tostes, R.C.; Webb, R.C. Internal pudendal artery from type 2 diabetic female rats demonstrate elevated endothelin-1-mediated constriction. J. Sex. Med. 2011, 8, 2472–2483. [Google Scholar] [CrossRef] [Green Version]
- Sánchez, A.; Martínez, P.; Muñoz, M.; Benedito, S.; García-Sacristán, A.; Hernández, M.; Prieto, D. Endothelin-1 contributes to endothelial dysfunction and enhanced vasoconstriction through augmented superoxide production in penile arteries from insulin-resistant obese rats: Role of ET(A) and ET(B) receptors. Br. J. Pharmacol. 2014, 171, 5682–5695. [Google Scholar] [CrossRef] [Green Version]
- Frederick, D.A.; Reynolds, T.A. The Value of Integrating Evolutionary and Sociocultural Perspectives on Body Image. Arch. Sex. Behav. 2021, 1–10. [Google Scholar] [CrossRef]
- Subramanian, S.V.; Perkins, J.M.; Khan, K.T. Do burdens of underweight and overweight coexist among lower socioeconomic groups in India? Am. J. Clin. Nutr. 2009, 90, 369–376. [Google Scholar] [CrossRef] [Green Version]
- Neuman, M.; Finlay, J.E.; Davey Smith, G.; Subramanian, S.V. The poor stay thinner: Stable socioeconomic gradients in BMI among women in lower- and middle-income countries. Am. J. Clin. Nutr. 2011, 94, 1348–1357. [Google Scholar] [CrossRef] [Green Version]
- Templin, T.; Cravo Oliveira Hashiguchi, T.; Thomson, B.; Dieleman, J.; Bendavid, E. The overweight and obesity transition from the wealthy to the poor in low- and middle-income countries: A survey of household data from 103 countries. PLoS Med. 2019, 16, e1002968. [Google Scholar] [CrossRef] [Green Version]
- Jones-Smith, J.C.; Gordon-Larsen, P.; Siddiqi, A.; Popkin, B.M. Is the burden of overweight shifting to the poor across the globe? Time trends among women in 39 low- and middle-income countries (1991–2008). Int. J. Obes. 2012, 36, 1114–1120. [Google Scholar] [CrossRef] [Green Version]
- Chen, D.; Jaenicke, E.C.; Volpe, R.J. Food Environments and Obesity: Household Diet Expenditure Versus Food Deserts. Am. J. Public Health 2016, 106, 881–888. [Google Scholar] [CrossRef]
- Parker, S.; Keim, K.S. Emic perspectives of body weight in overweight and obese white women with limited income. J. Nutr. Educ. Behav. 2004, 36, 282–289. [Google Scholar] [CrossRef]
- Panza, E.; Olson, K.; Goldstein, C.M.; Selby, E.A.; Lillis, J. Characterizing Lifetime and Daily Experiences of Weight Stigma among Sexual Minority Women with Overweight and Obesity: A Descriptive Study. Int. J. Environ. Res. Public Health 2020, 17, 4892. [Google Scholar] [CrossRef] [PubMed]
- Jensen, J.F.; Petersen, M.H.; Larsen, T.B.; Jørgensen, D.G.; Grønbaek, H.N.; Midtgaard, J. Young adult women’s experiences of body image after bariatric surgery: A descriptive phenomenological study. J. Adv. Nurs. 2014, 70, 1138–1149. [Google Scholar] [CrossRef]
- Song, P.; Patel, N.B.; Gunther, S.; Li, C.S.; Liu, Y.; Lee, C.Y.; Kludt, N.A.; Patel, K.B.; Ali, M.R.; Wong, M.S. Body Image & Quality of Life: Changes With Gastric Bypass and Body Contouring. Ann. Plast. Surg. 2016, 76 (Suppl. 3), S216–S221. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Jumbe, S.; Hamlet, C.; Meyrick, J. Psychological Aspects of Bariatric Surgery as a Treatment for Obesity. Curr. Obes. Rep. 2017, 6, 71–78. [Google Scholar] [CrossRef] [Green Version]
- Hameed, S.; Salem, V.; Tan, T.M.; Collins, A.; Shah, K.; Scholtz, S.; Ahmed, A.R.; Chahal, H. Beyond Weight Loss: Establishing a Postbariatric Surgery Patient Support Group-What Do Patients Want? J. Obes. 2018, 2018, 8419120. [Google Scholar] [CrossRef] [PubMed]
- Biörserud, C.; Shams, K.; Elander, A.; Fagevik Olsén, M. Self-image after bariatric surgery and its relationship to gender, excess skin and health-related quality of life. J. Plast. Surg. Hand Surg. 2018, 52, 288–293. [Google Scholar] [CrossRef]
- Masheb, R.M.; Grilo, C.M.; Burke-Martindale, C.H.; Rothschild, B.S. Evaluating oneself by shape and weight is not the same as being dissatisfied about shape and weight: A longitudinal examination in severely obese gastric bypass patients. Int. J. Eat Disord. 2006, 39, 716–720. [Google Scholar] [CrossRef] [PubMed]
- Frederick, D.A.; Garcia, J.R.; Gesselman, A.N.; Mark, K.P.; Hatfield, E.; Bohrnstedt, G. The Happy American Body 2.0: Predictors of affective body satisfaction in two U.S. national internet panel surveys. Body Image 2020, 32, 70–84. [Google Scholar] [CrossRef] [PubMed]
- Karazsia, B.T.; Murnen, S.K.; Tylka, T.L. Is body dissatisfaction changing across time? A cross-temporal meta-analysis. Psychol. Bull. 2017, 143, 293–320. [Google Scholar] [CrossRef] [PubMed]
- Frederick, D.A.; Buchanan, G.M.; Sadehgi-Azar, L.; Peplau, L.A.; Haselton, M.G.; Berezovskaya, A.; Lipinski, R.E. Desiring the muscular ideal: Men’s body satisfaction in the United States, Ukraine, and Ghana. Psychol. Men Masc. 2007, 8, 103–117. [Google Scholar] [CrossRef] [Green Version]
- Swenson, A.R.; Allen, K.R. My shape: Young men’s perceptions of their relationship to their bodies. Psychol. Men Masc. 2019, 20, 585–593. [Google Scholar] [CrossRef]
- Tylka, T.L. No harm in looking, right? Men’s pornography consumption, body image, and well-being. Psychol. Men Masc. 2015, 16, 97–107. [Google Scholar] [CrossRef] [Green Version]
- Richard, A.; Rohrmann, S.; Lohse, T.; Eichholzer, M. Is body weight dissatisfaction a predictor of depression independent of body mass index, sex and age? Results of a cross-sectional study. BMC Public Health 2016, 16, 863. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Gall, K.; van Zutven, K.; Lindstrom, J.; Bentley, C.; Gratwick-Sarll, K.; Harrison, C.; Lewis, V.; Mond, J. Obesity and emotional well-being in adolescents: Roles of body dissatisfaction, loss of control eating, and self-rated health. Obesity 2016, 24, 837–842. [Google Scholar] [CrossRef]
- Schvey, N.A.; Sbrocco, T.; Bakalar, J.L.; Ress, R.; Barmine, M.; Gorlick, J.; Pine, A.; Stephens, M.; Tanofsky-Kraff, M. The experience of weight stigma among gym members with overweight and obesity. Stigma Health 2017, 2, 292–306. [Google Scholar] [CrossRef]
- Puhl, R.M.; Himmelstein, M.S.; Pearl, R.L. Weight stigma as a psychosocial contributor to obesity. Am. Psychol. 2020, 75, 274–289. [Google Scholar] [CrossRef]
- Tylka, T.L.; Annunziato, R.A.; Burgard, D.; Daníelsdóttir, S.; Shuman, E.; Davis, C.; Calogero, R.M. The Weight-Inclusive versus Weight-Normative Approach to Health: Evaluating the Evidence for Prioritizing Well-Being over Weight Loss. J. Obes. 2014, 2014, 983495. [Google Scholar] [CrossRef]
- Cox, A.E.; Ullrich-French, S.; Tylka, T.L.; McMahon, A.K. The roles of self-compassion, body surveillance, and body appreciation in predicting intrinsic motivation for physical activity: Cross-sectional associations, and prospective changes within a yoga context. Body Image 2019, 29, 110–117. [Google Scholar] [CrossRef]
- Masters, W.H.; Johnson, V.E. Human Sexual Response; Little, Brown: Boston, MA, USA, 1966. [Google Scholar]
- Meana, M. Sexual Dysfunction in Women; Hogrefe Publishing: Cambridge, MA, USA, 2012. [Google Scholar]
- Kaplan, H.S. Disorders of Sexual Desire and Other New Concepts and Techniques in Sex Therapy; Brunner/Mazel: New York, NY, USA, 1979; Volume 2. [Google Scholar]
- Kaplan, H.S. Sexual Desire Disorders: Dysfunctional Regulation of Sexual Motivation; Routledge: New York, NY, USA, 1995. [Google Scholar]
- Basson, R. The female sexual response: A different model. J. Sex Marital Ther. 2000, 26, 51–65. [Google Scholar] [CrossRef] [PubMed]
- Basson, R.; Brotto, L.A.; Laan, E.; Redmond, G.; Utian, W.H. Assessment and Management of Women’s Sexual Dysfunctions: Problematic Desire and Arousal. J. Sex. Med. 2005, 2, 291–300. [Google Scholar] [CrossRef]
- Bancroft, J.; Graham, C.A. The varied nature of women’s sexuality: Unresolved issues and a theoretical approach. Horm. Behav. 2011, 59, 717–729. [Google Scholar] [CrossRef] [PubMed]
- Bancroft, J.; Janssen, E. The dual control model of male sexual response: A theoretical approach to centrally mediated erectile dysfunction. Neurosci. Biobehav. Rev. 2000, 24, 571–579. [Google Scholar] [CrossRef]
- Janssen, E.; Vorst, H.; Finn, P.; Bancroft, J. The Sexual Inhibition (SIS) and Sexual Excitation (SES) Scales: I. Measuring sexual inhibition and excitation proneness in men. J. Sex Res. 2002, 39, 114–126. [Google Scholar] [CrossRef] [PubMed]
- Bancroft, J.; Graham, C.A.; Janssen, E.; Sanders, S.A. The dual control model: Current status and future directions. J. Sex Res. 2009, 46, 121–142. [Google Scholar] [CrossRef]
- Milhausen, R.R.; Graham, C.A.; Sanders, S.A.; Yarber, W.L.; Maitland, S.B. Validation of the Sexual Excitation/Sexual Inhibition Inventory for Women and Men. Arch. Sex. Behav. 2010, 39, 1091–1104. [Google Scholar] [CrossRef] [Green Version]
- Busby, D.M.; Leonhardt, N.D.; Leavitt, C.E.; Hanna-Walker, V. Challenging the standard model of sexual response: Evidence of a variable male sexual response cycle. J. Sex Res. 2020, 57, 848–859. [Google Scholar] [CrossRef]
- Leavitt, C.E.; Leonhardt, N.D.; Busby, D.M. Different ways to get there: Evidence of a variable female sexual response cycle. J. Sex Res. 2019, 56, 899–912. [Google Scholar] [CrossRef]
- Ghane, A.; Sweeny, K. Embodied health: A guiding perspective for research in health psychology. Health Psychol. Rev. 2013, 7, S159–S184. [Google Scholar] [CrossRef]
- Rowland, D.L.; Motofei, I. Cross Cultural Research: Opportunities and Strategies for Discovery. In Cultural Differences and the Practice of Sexual Medicine: A Guide for Sexual Health Practitioners; Rowland, D.L., Jannini, E.A., Eds.; Springer International Publishing: Cham, Switzerland, 2020. [Google Scholar]
- Çaynak, S.; Boyacıoğlu, N.E.; Temel, M. Body perception and sexuality of bariatric surgery patients. Perspect. Psychiatr. Care 2021, 57, 1266–1272. [Google Scholar] [CrossRef]
- Nilsson-Condori, E.; Järvholm, S.; Thurin-Kjellberg, A.; Hedenbro, J.; Friberg, B. A New Beginning: Young Women’s Experiences and Sexual Function 18 Months After Bariatric Surgery. Sex. Med. 2020, 8, 730–739. [Google Scholar] [CrossRef]
- Kinzl, J.F.; Trefalt, E.; Fiala, M.; Hotter, A.; Biebl, W.; Aigner, F. Partnership, sexuality, and sexual disorders in morbidly obese women: Consequences of weight loss after gastric banding. Obes. Surg. 2001, 11, 455–458. [Google Scholar] [CrossRef]
- Kolotkin, R.L.; Binks, M.; Crosby, R.D.; Østbye, T.; Gress, R.E.; Adams, T.D. Obesity and sexual quality of life. Obesity 2006, 14, 472–479. [Google Scholar] [CrossRef] [PubMed]
- Morotti, E.; Battaglia, B.; Paradisi, R.; Persico, N.; Zampieri, M.; Venturoli, S.; Battaglia, C. Body mass index, Stunkard Figure Rating Scale, and sexuality in young Italian women: A pilot study. J. Sex. Med. 2013, 10, 1034–1043. [Google Scholar] [CrossRef]
- McHugh, M.; Kasardo, A. Anti-fat Prejudice: The Role of Psychology in Explication, Education and Eradication. Sex Roles 2012, 66, 617–627. [Google Scholar] [CrossRef]
- Dickins, M.; Thomas, S.L.; King, B.; Lewis, S.; Holland, K. The role of the fatosphere in fat adults’ responses to obesity stigma: A model of empowerment without a focus on weight loss. Qual. Health Res. 2011, 21, 1679–1691. [Google Scholar] [CrossRef] [PubMed]
- Dickins, M.; Browning, C.; Feldman, S.; Thomas, S. Social inclusion and the Fatosphere: The role of an online weblogging community in fostering social inclusion. Sociol. Health Illn. 2016, 38, 797–811. [Google Scholar] [CrossRef] [Green Version]
- O’Hara, L.; Ahmed, H.; Elashie, S. Evaluating the impact of a brief Health at Every Size®-informed health promotion activity on body positivity and internalized weight-based oppression. Body Image 2021, 37, 225–237. [Google Scholar] [CrossRef]
- Neumark-Sztainer, D. The weight dilemma: A range of philosophical perspectives. Int. J. Obes. Relat. Metab. Disord. J. Int. Assoc. Study Obes. 1999, 23 (Suppl. 2), S31–S37. [Google Scholar] [CrossRef] [PubMed]
- Penney, T.L.; Kirk, S.F.L. The Health at Every Size paradigm and obesity: Missing empirical evidence may help push the reframing obesity debate forward. Am. J. Public Health 2015, 105, e38–e42. [Google Scholar] [CrossRef] [PubMed]
- Sabatini, F.; Ulian, M.D.; Perez, I.; Pinto, A.J.; Vessoni, A.; Aburad, L.; Benatti, F.B.; Lopes de Campos-Ferraz, P.; Coelho, D.; de Morais Sato, P.; et al. Eating Pleasure in a Sample of Obese Brazilian Women: A Qualitative Report of an Interdisciplinary Intervention Based on the Health at Every Size Approach. J. Acad. Nutr. Diet. 2019, 119, 1470–1482. [Google Scholar] [CrossRef] [PubMed]
- Provencher, V.; Bégin, C.; Tremblay, A.; Mongeau, L.; Corneau, L.; Dodin, S.; Boivin, S.; Lemieux, S. Health-At-Every-Size and eating behaviors: 1-year follow-up results of a size acceptance intervention. J. Am. Diet. Assoc. 2009, 109, 1854–1861. [Google Scholar] [CrossRef]
- Forman, E.M.; Butryn, M.L.; Manasse, S.M.; Crosby, R.D.; Goldstein, S.P.; Wyckoff, E.P.; Thomas, J.G. Acceptance-based versus standard behavioral treatment for obesity: Results from the mind your health randomized controlled trial. Obesity 2016, 24, 2050–2056. [Google Scholar] [CrossRef]
- Berman, M.; Morton, S.; Hegel, M. Health at Every Size and Acceptance and Commitment Therapy for Obese, Depressed Women: Treatment Development and Clinical Application. Clin. Soc. Work J. 2016, 44, 265–278. [Google Scholar] [CrossRef]
- Yilmaz, F.T.; Kumsar, A.K.; Demirel, G. The effect of body image on sexual quality of life in obese married women. Health Care Women Int. 2019, 40, 479–492. [Google Scholar] [CrossRef]
- Parchomiuk, M.; Kirenko, J. Sexual Satisfaction in Obese People. Sex. Cult. 2021, 25, 1588–1604. [Google Scholar] [CrossRef]
- Satinsky, S.; Dennis, B.; Reece, M.; Sanders, S.; Bardzell, S. My ‘Fat Girl Complex’: A preliminary investigation of sexual health and body image in women of size. Cult. Health Sex. 2013, 15, 710–725. [Google Scholar] [CrossRef]
- Kvalem, I.L.; Træen, B.; Markovic, A.; von Soest, T. Body Image Development and Sexual Satisfaction: A Prospective Study From Adolescence to Adulthood. J. Sex Res. 2019, 56, 791–801. [Google Scholar] [CrossRef] [PubMed]
- Sarwer, D.B.; Steffen, K.J. Quality of Life, Body Image and Sexual Functioning in Bariatric Surgery Patients. Eur. Eat. Disord. Rev. 2015, 23, 504–508. [Google Scholar] [CrossRef] [PubMed]
- Szymanski, D.M.; Moffitt, L.B.; Carr, E.R. Sexual Objectification of Women: Advances to Theory and Research 1ψ7. Couns. Psychol. 2010, 39, 6–38. [Google Scholar] [CrossRef]
- Steer, A.; Tiggemann, M. The Role of Self-Objectification in Women’s Sexual Functioning. J. Soc. Clin. Psychol. 2008, 27, 205–225. [Google Scholar] [CrossRef] [Green Version]
- Gillen, M.M.; Markey, C.H. A review of research linking body image and sexual well-being. Body Image 2019, 31, 294–301. [Google Scholar] [CrossRef] [PubMed]
- Carels, R.A.; Miller, J.C.; Hlavka, R.; Selensky, J.; Shonrock, A.M.T.; Ellis, J.M. Associations between husbands’ weight bias and related concerns and husbands’ and wives’ psychological and relationship outcomes. Body Image 2020, 35, 11–21. [Google Scholar] [CrossRef]
Research Questions |
---|
(1) What are the general pathophysiological effects and mechanisms of action for obesity? |
(2) How do obesity-mediated mechanisms impact sexual function specifically? |
(3) To what extent does obesity influence body image satisfaction and appraisal? |
(4) To what extent have obesity, body image, and sexual function been studied in tandem? |
(5) How have social movements (e.g., body positivity) characterized obesity and sexuality? |
Obesity/Health Terms | Subject Terms | Sexual Health Terms | Body Image Terms |
---|---|---|---|
Overweight | Human(s) | (Sexual) desire | Body image |
Obese | Women | (Sexual) arousal | Body (dis)satisfaction |
Obesity | Female | Orgasm | Body appreciation |
Diabetes (mellitus) | Men | Ejaculation | (Body image) appraisal |
Insulin resistance | Male | (Vaginal) lubrication | Weight stigma |
Adipose (tissue) | Rodent | Erection | Anxiety |
Adipocyte(s) | Murine | Sexual satisfaction | Depression |
Inflammation | (Sexual) pleasure | Fat acceptance | |
Glycemia | (Sexual) pain | Body positivity | |
Health at every size |
Pathophysiological Mechanism | Effects on Sexual Functioning/Response |
---|---|
Adipose Tissue Dysregulation | * Estrogen–androgen imbalance |
* Secretion of pro-inflammatory mediators | |
* Increased expression of aromatase (T → E2) | |
Poor Glycemic Control | * Alterations to vaginal epithelial tissue |
* Reduced expression of aquaporin proteins | |
* Insufficient vaginal lubrication | |
* Reduced production of prostatic and seminal fluid | |
Chronic, Systemic Inflammation | * Damage of penile and clitoral blood vessels |
* Reduced expression of nitric oxide (NO) | |
* Increased expression of pro-contractile molecules | |
* Reduced blood flow to genital tissues |
Factors Influencing Body Image | Effects on Psychosocial Well-Being |
---|---|
Weight Stigma | * May include workplace discrimination and disparaging comments [84] |
* Discrimination for weight can intersect with marginalized identities [85] | |
* Some women viewed excess weight as helpful during financial hardship [84] | |
* Stigma at the gym associated with unhealthy/rapid weight loss methods [99] | |
* Stigma increases maladaptive/binge eating and odds of weight gain [99,100] | |
Body Weight and Depression | * Body dissatisfaction predicts depression for all weight categories [97,98] |
* Weight not significant predictor when body dissatisfaction controlled [97,98] | |
Bariatric Surgery | * Some patients show improved body confidence after surgery [86,87] |
* Body weight preoccupation may not improve with weight loss [87] | |
* Suboptimal outcomes may be attributable to excess skin (ptosis) [90] | |
* Limitation: Longitudinal data are often not available beyond 6–12 months [88] | |
Appearance Evaluation | * Women experience pressures for thinness and stereotyped beauty [84,86,91] |
* Weight loss can reduce need for external validation or fears of judgment [86] | |
* Men pressured to increase muscularity by diet and weight training [93,94,95] | |
* For men, pornography use increases stereotyped body image ideals/goals [96] |
Research Findings |
---|
* Health at Every Size (HAES) programs improve mindfulness while eating [129,132] |
* HAES modalities reduce emotional eating and increase guiltless eating [129,130,131] |
* Body satisfaction predicts higher sexual quality of life for all weight classes [133] |
* Sexual satisfaction for obese women/men affected by sex behavior discrepancies [134] |
* Sexual pleasure higher for overweight women with internalized body confidence [135] |
* Weight loss may increase sex frequency/pleasure, but results are inconsistent [119,120] |
* Negative obesity effects on sexual function more likely for highest obese classes [121] |
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. |
© 2022 by the author. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Share and Cite
McNabney, S.M. Obesity, Body Image Dissatisfaction, and Sexual Dysfunction: A Narrative Review. Sexes 2022, 3, 20-39. https://doi.org/10.3390/sexes3010002
McNabney SM. Obesity, Body Image Dissatisfaction, and Sexual Dysfunction: A Narrative Review. Sexes. 2022; 3(1):20-39. https://doi.org/10.3390/sexes3010002
Chicago/Turabian StyleMcNabney, Sean M. 2022. "Obesity, Body Image Dissatisfaction, and Sexual Dysfunction: A Narrative Review" Sexes 3, no. 1: 20-39. https://doi.org/10.3390/sexes3010002
APA StyleMcNabney, S. M. (2022). Obesity, Body Image Dissatisfaction, and Sexual Dysfunction: A Narrative Review. Sexes, 3(1), 20-39. https://doi.org/10.3390/sexes3010002