Skip to main content

GENERAL COMMENTARY article

Front. Endocrinol., 10 September 2024
Sec. Clinical Diabetes
This article is part of the Research Topic Strategies to Overcome Metabolic Syndrome and Related Diseases View all 16 articles

Commentary: A rapid action plan to improve diagnosis and management of lipodystrophy syndromes

  • 1Department of Inflammation and Immunity, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, United States
  • 2Center for Microbiome and Human Health, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, United States
  • 3Department of Medicine, Division of Diabetes, Endocrinology and Metabolism, Vanderbilt University Medical Center, Nashville, TN, United States

A commentary on
A rapid action plan to improve diagnosis and management of lipodystrophy syndromes

By Fourman LT, Lima JG, Simha V, Cappa M, Alyaarubi S, Montenegro Jr. R, Akinci B and Santini F (2024). Front. Endocrinol. 15:1383318. doi: 10.3389/fendo.2024.1383318

1 Introduction

Fourman et al. have recently published a clinically-oriented rapid action plan for the diagnosis and management of lipodystrophy syndromes (1). Lipodystrophy syndromes may be characterized by two factors: the pattern of fat loss which may occur across the whole body (generalized) or in specific body parts (partial) and whether the condition is genetic (congenital/familial) or acquired (2, 3). Unlike their clinical antithesis, obesity, lipodystrophy syndromes are rare, has heterogeneous clinical presentation, and are challenging to diagnose, yet the metabolic complications and end-organ damage that result from these two conditions can be similar. It took an average of 3.1 years in generalized lipodystrophy and 9.0 years in partial lipodystrophy for physicians to diagnose them accurately (4). Fourman et al. developed the quick action plan based on a large-scale study of comprehensive and long-term data across multiple countries (1, 4). An international panel of clinical experts were invited to discuss the key priorities for clinicians in the first 100 days after seeing a patient with clinical suspicion for the diagnosis (1). In comparison to the previous version of “step-by-step approach to diagnosis and treatment of lipodystrophy” (5), the rapid action plan has been updated with more detailed guidance for early diagnosis including the criteria for the skin thickness in men and women, which is considered important for early screening and can be precisely measured with dual-energy x-ray absorptiometry (1). Although the lack of adipose tissue is required for diagnosis of a lipodystrophy syndrome, common indicators that healthcare providers should watch for in their routine assessment of patients include features of metabolic syndrome such as insulin resistance, hypertriglyceridemia, fatty liver disease, and polycystic ovarian syndrome (PCOS) that is disproportionate to body size (i.e., in the absence of increased adiposity).

Treatment of lipodystrophies generally includes addressing the body’s inability to properly store lipid by limiting dietary fat, supplementation of adipokines, and common treatments for affected organs. The ultimate goal of the rapid action plan proposed by Fourman et al. is to improve the diagnosis for lipodystrophy syndromes to enable earlier and more consistent treatment for patients.

A prompt action in diagnosis and treatment for lipodystrophy can provide clinical data of the disease in its early stages, which is currently scarce due to its rarity and heterogeneity. Clinical data for lipodystrophy at its early stages are important to explore therapeutic strategies not only for lipodystrophy syndromes but also for diabetic obesity. The metabolic reflection of the lack of adipose tissue is similar in diabetic obesity, in line with the concept that the functional capacity of adipose tissue in diabetic obesity has been overwhelmed by nutrition. Lipodystrophies and diabetic obesity together highlight the critical roles of adipose tissue in metabolism. Research in lipodystrophy syndromes may provide critical information to explore novel therapeutic strategies for diabetic obesity. For example, metabolic disorders are reduced by leptin replacement therapy in generalized lipodystrophy patients (6, 7), which makes strategies of increasing signaling sensitivity to adipokines appealing to improve metabolic complications in diabetic obesity because adipokine levels are generally high in those patients.

2 Relevance to other concomitant diseases

While the Fourman et al. rapid action plan focuses on the clinical diagnosis and management of the metabolic consequences of lipodystrophy syndromes, it is important to note that other concomitant disease states may also contribute to lipodystrophy. These states include neurological diseases, autoimmune disorders, and inflammatory bowel diseases (IBD). Given the numerous insights lipodystrophy syndromes have provided in the metabolic disease space, further consideration should be given to lipodystrophies’ mechanistic relationships to other disease processes.

There have been reports of concomitant neurological diseases with lipodystrophy syndromes including a case report where a patient with congenital partial lipodystrophy and cataracts presented with paresthesia in the lower limbs and abnormal gait (8). Upon further investigation, the authors concluded that based on family history, the syndrome was likely autosomal dominant, but could not identify the underlying genetics. Subsequently, a study of six children carrying the c.985C>T mutation in the BSCL2 (Seipin) gene lead to the association of the mutation with fatal neurodegeneration in homozygous carriers and this mutation was linked to exon 7-skipping transcripts of this gene (9). Most recently, a case series describing patients with a form of congenital generalized lipodystrophy presented with progressive myoclonus epilepsy was reported and attributed to novel mutations in the BSCL2 (Seipin) gene (10). Importantly, none of these reports sought to understand the mechanistic basis of these neurological conditions with the lipodystrophy syndrome.

With respect to autoimmunity, it has been described that acquired generalized lipodystrophy can co-occur with type 1 diabetes. In a report of two such cases, the patients developed both conditions in prepubescence and exhibited poor glycemic control on insulin alone; however following a year of metreleptin treatment, both children had marked improvements in glycemic control with lower insulin requirements (7). Generalized lipodystrophy has also been acquired in pediatric patients with Hashimoto’s thyroiditis, rheumatoid arthritis, hemolytic anemia, and chronic hepatitis (6). In these cases, metreleptin therapy improved metabolic parameters, but did not affect the clinical course of the autoimmune conditions. The best described relationship between autoimmunity and lipodystrophies involves the C3 nephritic factor and acquired partial lipodystrophy. In these cases it was observed that autoimmune conditions such as systemic lupus erythematosus, dermatomyositis, and membranoproliferative glomerulonephritis consequently occurred with upper body partial lipodystrophy (11, 12). In three cases of chronic hepatitis with features of autoimmunity where patients developed generalized lipodystrophy, the mechanism of the observed low C4 complement factor levels was investigated. These studies showed that while the few patients had differing etiologies of autoimmunity constitutive activation of the alternative complement pathway appeared to be common between these cases (13). Collectively these reports indicate that both partial and general lipodystrophy syndromes do co-occur with numerous autoimmune conditions and therefore may influence one another.

There is a known relationship between adipose tissue and Crohn’s disease, one of the two main types of IBD. In Crohn’s disease there is an expansion of mesenteric adipose tissue that wraps around the diseased bowel wall, termed “creeping fat” (14, 15). Notably, there were two case reports in 2019 related to generalized lipodystrophy syndromes and Crohn’s disease. In the first case a pediatric patient with congenital generalized lipodystrophy experienced bowel perforation, which was associated with smooth muscle hypertrophy (16). The other report discussed a patient that experienced TNFα-dependent inflammation as a result of recombinant leptin therapy (17). Given the studies that have shown the contribution of adipose tissue to Crohn’s disease further work is warranted to clarify the molecular basis underpinning the role of lipodystrophy in Crohn’s disease pathology.

3 Conclusions

While Fourman et al. provide an up-to-date action plan for the clinical diagnosis and management of lipodystrophy syndromes’ numerous adverse metabolic consequences, there remains little work done in basic and translational research to understand the relationship between lipodystrophy syndromes and other concomitant conditions. Given the burden described in the studies cited above, especially in pediatric patients, and the tremendous insights that lipodystrophy syndromes have provided in the context of metabolic disease as well as adipose and lipid biology, greater consideration should be given to the role of adipose tissue cross talk with other organs involved in these concomitant conditions. Importantly, there are animal models available for lipodystrophies (1820), which can facilitate such studies.

Author contributions

WM: Conceptualization, Visualization, Writing – original draft, Writing – review & editing. LZ: Conceptualization, Funding acquisition, Visualization, Writing – review & editing.

Funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. WM is supported by a Cleveland Clinic Global Center for Pathogen and Human Health Research Postdoctoral Fellowship. LZ is supported by NIA (K01AG077038).

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. Fourman LT, Lima JG, Simha V, Cappa M, Alyaarubi S, Montenegro R Jr., et al. A rapid action plan to improve diagnosis and management of lipodystrophy syndromes. Front Endocrinol (Lausanne). (2024) 15:1383318. doi: 10.3389/fendo.2024.1383318

PubMed Abstract | Crossref Full Text | Google Scholar

2. Garg A. Acquired and inherited lipodystrophies. New Engl J Med. (2004) 350:1220–34. doi: 10.1056/NEJMra025261

PubMed Abstract | Crossref Full Text | Google Scholar

3. Simha V, Garg A. Lipodystrophy: lessons in lipid and energy metabolism. Curr Opin Lipidol. (2006) 17:162–9. doi: 10.1097/01.mol.0000217898.52197.18

PubMed Abstract | Crossref Full Text | Google Scholar

4. Akinci B, Oral EA, Neidert A, Rus D, Cheng WY, Thompson-Leduc P, et al. Comorbidities and survival in patients with lipodystrophy: an international chart review study. J Clin Endocrinol Metab. (2019) 104:5120–35. doi: 10.1210/jc.2018-02730

PubMed Abstract | Crossref Full Text | Google Scholar

5. Araújo-Vilar D, Santini F. Diagnosis and treatment of lipodystrophy: a step-by-step approach. J Endocrinol Invest. (2019) 42:61–73. doi: 10.1007/s40618-018-0887-z

PubMed Abstract | Crossref Full Text | Google Scholar

6. Lebastchi J, Ajluni N, Neidert A, Oral EA. A report of three cases with acquired generalized lipodystrophy with distinct autoimmune conditions treated with metreleptin. J Clin Endocrinol Metab. (2015) 100:3967–70. doi: 10.1210/jc.2015-2589

PubMed Abstract | Crossref Full Text | Google Scholar

7. Park JY, Chong AY, Cochran EK, Kleiner DE, Haller MJ, Schatz DA, et al. Type 1 diabetes associated with acquired generalized lipodystrophy and insulin resistance: the effect of long-term leptin therapy. J Clin Endocrinol Metab. (2008) 93:26–31. doi: 10.1210/jc.2007-1856

PubMed Abstract | Crossref Full Text | Google Scholar

8. Berger JR, Arioglu Oral E, Taylor SI. Familial lipodystrophy associated with neurodegeneration and congenital cataracts. Neurology. (2002) 58:43–7. doi: 10.1212/WNL.58.1.43

PubMed Abstract | Crossref Full Text | Google Scholar

9. Guillén-Navarro E, Sánchez-Iglesias S, Domingo-Jiménez R, Victoria B, Ruiz-Riquelme A, Rábano A, et al. A new seipin-associated neurodegenerative syndrome. J Med Genet. (2013) 50:401–9. doi: 10.1136/jmedgenet-2013-101525

PubMed Abstract | Crossref Full Text | Google Scholar

10. Opri R, Fabrizi GM, Cantalupo G, Ferrarini M, Simonati A, Dalla Bernardina B, et al. Progressive Myoclonus Epilepsy in Congenital Generalized Lipodystrophy type 2: Report of 3 cases and literature review. Seizure. (2016) 42:1–6. doi: 10.1016/j.seizure.2016.08.008

PubMed Abstract | Crossref Full Text | Google Scholar

11. Misra A, Peethambaram A, Garg A. Clinical features and metabolic and autoimmune derangements in acquired partial lipodystrophy: report of 35 cases and review of the literature. Medicine. (2004) 83:18–34. doi: 10.1097/01.md.0000111061.69212.59

PubMed Abstract | Crossref Full Text | Google Scholar

12. Sissons JGP, West RJ, Fallows J, Williams DG, Boucher BJ, Amos N, et al. The complement abnormalities of lipodystrophy. New Engl J Med. (1976) 294:461–5. doi: 10.1056/NEJM197602262940902

PubMed Abstract | Crossref Full Text | Google Scholar

13. Savage DB, Semple RK, Clatworthy MR, Lyons PA, Morgan BP, Cochran EK, et al. Complement abnormalities in acquired lipodystrophy revisited. J Clin Endocrinol Metab. (2009) 94:10–6. doi: 10.1210/jc.2008-1703

PubMed Abstract | Crossref Full Text | Google Scholar

14. Kredel LI, Siegmund B. Adipose-tissue and intestinal inflammation – visceral obesity and creeping fat. Front Immunol. (2014) 5:462. doi: 10.3389/fimmu.2014.00462

PubMed Abstract | Crossref Full Text | Google Scholar

15. Sheehan AL, Warren BF, Gear MWL, Shepherd NA. Fat-wrapping in Crohn’s disease: Pathological basis and relevance to surgical practice. Br J Surg. (2005) 79:955–8. doi: 10.1002/bjs.1800790934

Crossref Full Text | Google Scholar

16. Muñoz A, Radulescu A, Baerg J, Mendez Y, Khan FA. Bowel perforation in a pediatric patient with congenital generalized lipodystrophy type 4. J Pediatr Surg Case Rep. (2019) 48:101257. doi: 10.1016/j.epsc.2019.101257

Crossref Full Text | Google Scholar

17. Ziegler JF, Böttcher C, Letizia M, Yerinde C, Wu H, Freise I, et al. Leptin induces TNFα-dependent inflammation in acquired generalized lipodystrophy and combined Crohn’s disease. Nat Commun. (2019) 10:5629. doi: 10.1038/s41467-019-13559-7

PubMed Abstract | Crossref Full Text | Google Scholar

18. Kim S, Huang L-W, Snow KJ, Ablamunits V, Hasham MG, Young TH, et al. A mouse model of conditional lipodystrophy. Proc Natl Acad Sci. (2007) 104:16627–32. doi: 10.1073/pnas.0707797104

PubMed Abstract | Crossref Full Text | Google Scholar

19. Le Lay S, Magré J, Prieur X. Not enough fat: mouse models of inherited lipodystrophy. Front Endocrinol. (2022) 13:785819. doi: 10.3389/fendo.2022.785819

Crossref Full Text | Google Scholar

20. Pajvani UB, Trujillo ME, Combs TP, Iyengar P, Jelicks L, Roth KA, et al. Fat apoptosis through targeted activation of caspase 8: a new mouse model of inducible and reversible lipoatrophy. Nat Med. (2005) 11:797–803. doi: 10.1038/nm1262

PubMed Abstract | Crossref Full Text | Google Scholar

Keywords: lipodystrophy syndromes, adipose tissue, concomitant disease, rare endocrine disorders, metabolic disease, diabetic obesity

Citation: Massey WJ and Zhu L (2024) Commentary: A rapid action plan to improve diagnosis and management of lipodystrophy syndromes. Front. Endocrinol. 15:1445226. doi: 10.3389/fendo.2024.1445226

Received: 07 June 2024; Accepted: 26 August 2024;
Published: 10 September 2024.

Edited by:

Habib Yaribeygi, Semnan University of Medical Sciences, Iran

Reviewed by:

Flavia Prodam, University of Eastern Piedmont, Italy
Phiwayinkosi V. Dludla, South African Medical Research Council, South Africa

Copyright © 2024 Massey and Zhu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: William J. Massey, masseyw2@ccf.org; Lin Zhu, lin.zhu@vumc.org

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.