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COVID-19 / SPECIALTY RESEARCH

EndocrinologyIn perspective.

The key COVID-19 findings in endocrinology, distilled into a clear, readable brief. The evidence is here whenever you want to go deeper.

INSIDE THIS MONITOR
29cited sources
13available findings

Study findings updated

AI-assisted evidence summary. For general information. These findings are not individual medical advice or a clinician endorsement.

THE SHORT VERSION

What’s worth knowing.

The key findings, what they mean, and the context that matters.

THE HEADLINE TAKEAWAY41%higher relative risk

COVID-19 survivors had higher new-onset diabetes risk

In a systematic review and meta-analysis, COVID-19 survivors had a 41% higher relative risk of new-onset diabetes than non-infected individuals.

This pooled post-acute result is relative, not absolute. Follow-up, population details, and underlying study designs are not available in this summary, so it should not be read as causal.

See the evidence

41% higher relative risk, calculated from RR 1.41. This is not an absolute percentage-point difference.

41% increased risk of new-onset diabetes in COVID-19 survivors compared to non-infected individuals

RR 1.41
95% CI: 1.38-1.44

Lawal, Bukola et al.. Post-acute metabolic changes and risk of new-onset diabetes following COVID-19: a systematic review and meta-analysis.. Frontiers in endocrinology. 2026.

Increased insulin resistance measured by HOMA-IR

SMD 0.96
95% CI: 0.33-1.58

Lawal, Bukola et al.. Post-acute metabolic changes and risk of new-onset diabetes following COVID-19: a systematic review and meta-analysis.. Frontiers in endocrinology. 2026.

Elevated HbA1c levels indicating impaired glycemic control

SMD 1.44
95% CI: 0.36-2.52

Lawal, Bukola et al.. Post-acute metabolic changes and risk of new-onset diabetes following COVID-19: a systematic review and meta-analysis.. Frontiers in endocrinology. 2026.

02

HbA1c showed no clear change at 12 months

Among adults without preexisting diabetes, HbA1c was 5.39% before infection and 5.40% at 12 months after COVID-19, with no established difference.

This is a longitudinal within-group comparison. The same study reported metabolic-syndrome incidence and increased estimated cardiovascular risk, so HbA1c does not represent every metabolic outcome.

See the evidence

HbA1c from pre-infection to 12 months after COVID-19 among adults without preexisting diabetes

5.39% vs 5.40%; P = .435

Daher, Joviane et al.. Glucose metabolism across COVID-19 and long COVID: a longitudinal study.. Journal of the Endocrine Society. 2026.

Added

New-onset metabolic syndrome incidence across long COVID categories; persistent metabolic syndrome was more frequent with more severe long COVID

18%-20%

Daher, Joviane et al.. Glucose metabolism across COVID-19 and long COVID: a longitudinal study.. Journal of the Endocrine Society. 2026.

Added

Change in estimated 10-year ASCVD risk after COVID-19

6.7% to 7.3%; P < .001

Daher, Joviane et al.. Glucose metabolism across COVID-19 and long COVID: a longitudinal study.. Journal of the Endocrine Society. 2026.

Added

03

Glucose variability was linked to short-term hospital mortality

A meta-analysis found that high glucose variability was associated with short-term all-cause mortality among hospitalized COVID-19 patients.

The reference glucose-variability group is not available in this summary, so the pooled relative-risk estimate is not featured. The association does not establish that variability caused death.

See the evidence

High glucose variability associated with increased short-term all-cause mortality in hospitalized COVID-19 patients

RR 2.10
95% CI: 1.69-2.59

Wang, Zixuan et al.. Glycemic variability and the short-term mortality of hospitalized patients with COVID-19: a meta-analysis.. Frontiers in endocrinology. 2026.

Association in younger patients (mean age <62 years)

RR 1.78

Wang, Zixuan et al.. Glycemic variability and the short-term mortality of hospitalized patients with COVID-19: a meta-analysis.. Frontiers in endocrinology. 2026.

Stronger association in older patients (mean age ≥62 years)

RR 2.79

Wang, Zixuan et al.. Glycemic variability and the short-term mortality of hospitalized patients with COVID-19: a meta-analysis.. Frontiers in endocrinology. 2026.

Study-specific findings. Different populations, treatments and follow-up periods can produce different results.

THE RESEARCH, AS IT ARRIVES

Latest studies.

The newest findings added to this collection.
The learning from each, already distilled.

  1. STUDY 01Findings added
    TL;DR

    Stable HbA1c coexisted with other metabolic findings

    Among adults without preexisting diabetes, HbA1c was 5.39% before infection and 5.40% at 12 months, with no established change.

    The study also reported new-onset metabolic syndrome in 18%-20% across long-COVID categories, with persistence more frequent at greater severity, and estimated 10-year cardiovascular risk rising from 6.7% to 7.3%. The latter is not an observed event rate.

    Study details & original results

    Daher, Joviane et al.. Glucose metabolism across COVID-19 and long COVID: a longitudinal study.. Journal of the Endocrine Society. 2026.

    HbA1c from pre-infection to 12 months after COVID-19 among adults without preexisting diabetes

    5.39% vs 5.40%; P = .435

    New-onset metabolic syndrome incidence across long COVID categories; persistent metabolic syndrome was more frequent with more severe long COVID

    18%-20%

    Change in estimated 10-year ASCVD risk after COVID-19

    6.7% to 7.3%; P < .001

    Citation in Endocrinology
1 of 1 study updates

Dates show when findings were added here, not when papers were published. Study populations and comparisons differ.

WHEN YOU WANT TO GO DEEPER
See all 13 findingsOriginal results, comparisons and study details.
5 of 5 source groupsFindings stay together with their study.
SOURCE 293 findings

Daher, Joviane et al.. Glucose metabolism across COVID-19 and long COVID: a longitudinal study.. Journal of the Endocrine Society. 2026.

HbA1c from pre-infection to 12 months after COVID-19 among adults without preexisting diabetes

Added
5.39% vs 5.40%; P = .435Source [29]

Change in estimated 10-year ASCVD risk after COVID-19

Added
6.7% to 7.3%; P < .001Source [29]
All 3 findings from this source

New-onset metabolic syndrome incidence across long COVID categories; persistent metabolic syndrome was more frequent with more severe long COVID

Added
SOURCE 263 findings

Qian, Jiahui et al.. New-onset diabetes following SARS-CoV-2 infection in the Omicron era: a matched cohort study.. International journal of epidemiology. 2026.

New-onset diabetes treatment initiation after SARS-CoV-2 infection in Omicron era

HR 1.1495% CI: 1.12-1.17Source [26]

Risk of initiating diabetes treatment after COVID-19 during Omicron-dominant period

HR 1.1495% CI: 1.12-1.17Source [26]
All 3 findings from this source

Diabetes risk for those with booster within 90 days

HR 1.0895% CI: 1.04-1.12Source [26]
SOURCE 273 findings

Lawal, Bukola et al.. Post-acute metabolic changes and risk of new-onset diabetes following COVID-19: a systematic review and meta-analysis.. Frontiers in endocrinology. 2026.

41% increased risk of new-onset diabetes in COVID-19 survivors compared to non-infected individuals

RR 1.4195% CI: 1.38-1.44Source [27]

Elevated HbA1c levels indicating impaired glycemic control

SMD 1.4495% CI: 0.36-2.52Source [27]
All 3 findings from this source

Increased insulin resistance measured by HOMA-IR

SMD 0.9695% CI: 0.33-1.58Source [27]
SOURCE 283 findings

Wang, Zixuan et al.. Glycemic variability and the short-term mortality of hospitalized patients with COVID-19: a meta-analysis.. Frontiers in endocrinology. 2026.

High glucose variability associated with increased short-term all-cause mortality in hospitalized COVID-19 patients

RR 2.1095% CI: 1.69-2.59Source [28]

Stronger association in older patients (mean age ≥62 years)

All 3 findings from this source

Association in younger patients (mean age <62 years)

Browse the 29 original sourcesThe complete bibliography behind this monitor.
  1. [1]

    Xie Y, Al-Aly Z. Risks and burdens of incident diabetes in long COVID: a cohort study. Lancet Diabetes Endocrinol. 2022;10(5):311-321.

    Open original source in a new tab
  2. [2]

    Rathmann W, Kuss O, Kostev K. Incidence of newly diagnosed diabetes after COVID-19. Diabetologia. 2022;65(6):949-954.

    Open original source in a new tab
  3. [3]

    Bowe B, Xie Y, Al-Aly Z. Acute and postacute sequelae associated with SARS-CoV-2 reinfection. Nat Med. 2022;28(11):2398-2405.

    Open original source in a new tab
  4. [4]

    Rubino F, Amiel SA, Zimmet P, et al. New-onset diabetes in COVID-19. N Engl J Med. 2020;383(8):789-790.

    Open original source in a new tab
  5. [5]

    Muller JA, Gross R, Conzelmann C, et al. SARS-CoV-2 infects and replicates in cells of the human endocrine and exocrine pancreas. Nat Metab. 2021;3(2):149-165.

    Open original source in a new tab
  6. [6]

    Tang X, Uhl S, Zhang T, et al. SARS-CoV-2 infection induces beta cell transdifferentiation. Cell Metab. 2021;33(8):1577-1591.

    Open original source in a new tab
  7. [7]

    Wu CT, Lidsky PV, Xiao Y, et al. SARS-CoV-2 infects human pancreatic beta cells and elicits beta cell impairment. Cell Metab. 2021;33(8):1565-1576.

    Open original source in a new tab
  8. [8]

    Lania A, Sandri MT, Cellini M, et al. Thyrotoxicosis in patients with COVID-19: the THYRCOV study. Eur J Endocrinol. 2020;183(4):381-387.

    Open original source in a new tab
  9. [9]

    Chen M, Zhou W, Xu W. Thyroid function analysis in 50 patients with COVID-19: a retrospective study. Thyroid. 2021;31(1):8-11.

    Open original source in a new tab
  10. [10]

    Brancatella A, Ricci D, Viola N, et al. Subacute thyroiditis after SARS-CoV-2 infection. J Clin Endocrinol Metab. 2020;105(7):dgaa276.

    Open original source in a new tab
  11. [11]

    Tan T, Khoo B, Mills EG, et al. Association between high serum total cortisol concentrations and mortality from COVID-19. Lancet Diabetes Endocrinol. 2020;8(8):659-660.

    Open original source in a new tab
  12. [12]

    Hashim M, Athar S, Gaba WH. New onset adrenal insufficiency in a patient with COVID-19. BMJ Case Rep. 2021;14(1):e237690.

    Open original source in a new tab
  13. [13]

    Leow MK, Kwek DS, Ng AW, et al. Hypocortisolism in survivors of severe acute respiratory syndrome (SARS). Clin Endocrinol (Oxf). 2005;63(2):197-202.

    Open original source in a new tab
  14. [14]

    Kamrath C, Rosenbauer J, Eckert AJ, et al. Incidence of type 1 diabetes in children and adolescents during the COVID-19 pandemic in Germany. JAMA. 2022;328(8):790-792.

    Open original source in a new tab
  15. [15]

    Barrett CE, Koyama AK, Alvarez P, et al. Risk for newly diagnosed diabetes >30 days after SARS-CoV-2 infection among persons aged <18 years. MMWR Morb Mortal Wkly Rep. 2022;71(2):59-65.

    Open original source in a new tab
  16. [16]

    Ssentongo P, Zhang Y, Witmer L, et al. Association of COVID-19 with diabetes: a systematic review and meta-analysis. Sci Rep. 2022;12(1):20191.

    Open original source in a new tab
  17. [17]

    Lui DTW, Lee CH, Chow WS, et al. Thyroid dysfunction in relation to immune profile, disease status, and outcome in 191 patients with COVID-19. J Clin Endocrinol Metab. 2021;106(2):e926-e935.

    Open original source in a new tab
  18. [18]

    American Diabetes Association. Standards of Care in Diabetes - 2024. Diabetes Care. 2024;47(Suppl 1):S1-S321.

    Open original source in a new tab
  19. [19]

    CoviDIAB Project. International registry for new-onset diabetes in COVID-19. www.covidiab.e-dendrite.com

    Original source link unavailable
  20. [20]

    Al-Aly Z, Xie Y, Bowe B. High-dimensional characterization of post-acute sequelae of COVID-19. Nature. 2021;594(7862):259-264.

    Open original source in a new tab
  21. [21]

    Ayoubkhani D, Khunti K, Nafilyan V, et al. Post-covid syndrome in individuals admitted to hospital with COVID-19. BMJ. 2021;372:n693.

    Open original source in a new tab
  22. [22]

    Clarke SA, Abbara A, Dhillo WS. Impact of COVID-19 on the endocrine system: a mini-review. Endocrinology. 2022;163(1):bqab203.

    Open original source in a new tab
  23. [23]

    Montefusco L, Ben Nasr M, D'Addio F, et al. Acute and long-term disruption of glycometabolic control after SARS-CoV-2 infection. Nat Metab. 2021;3(6):774-785.

    Open original source in a new tab
  24. [24]

    Sathish T, Kapoor N, Cao Y, et al. Proportion of newly diagnosed diabetes in COVID-19 patients: a systematic review and meta-analysis. Diabetes Obes Metab. 2021;23(3):870-874.

    Open original source in a new tab
  25. [25]

    Wroblewski I, et al. Type 1 diabetes risk in children following COVID-19 infection - Norwegian cohort study. 2024.

    Original source link unavailable
  26. [26]

    Qian, Jiahui et al.. New-onset diabetes following SARS-CoV-2 infection in the Omicron era: a matched cohort study.. International journal of epidemiology. 2026.

    Open original source in a new tab
  27. [27]

    Lawal, Bukola et al.. Post-acute metabolic changes and risk of new-onset diabetes following COVID-19: a systematic review and meta-analysis.. Frontiers in endocrinology. 2026.

    Open original source in a new tab
  28. [28]

    Wang, Zixuan et al.. Glycemic variability and the short-term mortality of hospitalized patients with COVID-19: a meta-analysis.. Frontiers in endocrinology. 2026.

    Open original source in a new tab
  29. [29]

    Daher, Joviane et al.. Glucose metabolism across COVID-19 and long COVID: a longitudinal study.. Journal of the Endocrine Society. 2026.

    Open original source in a new tab
ABOUT THIS MONITOR

Understanding includes the limits.

This is an AI-assisted evidence summary, not a clinician endorsement. Read each original paper for its complete methods, population and limitations. Different studies can ask different questions and report different kinds of results.

Dates marked “added” describe when a finding entered this monitor, not when the study was published or clinically reviewed. Personal health and treatment decisions belong in a conversation with a qualified clinician.

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