Review History


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Summary

  • The initial submission of this article was received on November 28th, 2024 and was peer-reviewed by 2 reviewers and the Academic Editor.
  • The Academic Editor made their initial decision on January 21st, 2025.
  • The first revision was submitted on January 31st, 2025 and was reviewed by 1 reviewer and the Academic Editor.
  • The article was Accepted by the Academic Editor on February 3rd, 2025.

Version 0.2 (accepted)

· Feb 3, 2025 · Academic Editor

Accept

Thank you for addressing all the reviewers comments. At this time, this version of your article does not require further changes,

Reviewer 2 ·

Basic reporting

no comment

Experimental design

no comment

Validity of the findings

no comment

Additional comments

no comment

Version 0.1 (original submission)

· Jan 21, 2025 · Academic Editor

Minor Revisions

This is a well-designed, well-executed, and well-written research paper.
However, there are some reviewer comments that need to be revised, please make these changes to improve the quality of your article.

Reviewer 1 ·

Basic reporting

It is a clear, concise, and well-written manuscript. However, the authors need to incorporate and revise certain aspects of their manuscript:
• Lines 79-81: It is suggested that reference 1 be replaced with the most recent one. “The global diabetes prevalence in 20-79-year old in 2021 was estimated to be 10.5% (536.6 million people), rising to 12.2% (783.2 million) in 2045” by Sun H, Saeedi P, Karuranga S, Pinkepank M, Ogurtsova K, Duncan BB, Stein C, Basit A, Chan JCN, Mbanya JC, Pavkov ME, Ramachandaran A, Wild SH, James S, Herman WH, Zhang P, Bommer C, Kuo S, Boyko EJ, Magliano DJ. IDF Diabetes Atlas: Global, regional and country-level diabetes prevalence estimates for 2021 and projections for 2045. Diabetes Res Clin Pract. 2022 Jan;183:109119. doi: 10.1016/j.diabres.2021.109119. Epub 2021 Dec 6. Erratum in: Diabetes Res Clin Pract. 2023 Oct;204:110945. doi: 10.1016/j.diabres.2023.110945. PMID: 34879977; PMCID: PMC11057359.
• Lines 99-100: A brief description of CVAI is needed.
• Lines104-106: the aims of this study need to be clarified.
• Lines 111-112: Most recent publications used type 2 diabetes (T2D) instead of type 2 diabetes mellitus (T2DM).
• Lines 136-137: A reference for the “Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation” is needed

Experimental design

Exclusion criteria

• Lines 113-117: Did you exclude diabetic patients who have hypertension and are taking antihypertensive drugs, which might increase serum uric acid, such as thiazide-type diuretics, β blockers, ACE, and ARBs?

Validity of the findings

• Line 195: It is advisable to mention that age and estimated glomerular filtration rate (eGFR) had a significant negative correlation with hyperuricemia.
• Lines 239-240: Can you please mention the cutoff point for the basic model and +CVAI in Table 4
• It is advisable to add a paragraph about hypertension and HUA, especially the medication used for the treatment of hypertension

Reviewer 2 ·

Basic reporting

No comment

Experimental design

No comment

Validity of the findings

No comment

Additional comments

In Figure 3, instead of HDL, there should be HDL-C and instead of LDL - LDL-C.

I do not see the need for the authors to explain the abbreviations that have already been explained once constantly; this mainly concerns laboratory parameters and the studied index (CVAI). I suggest the authors read the papers in this regard and catch these errors.

I believe that as a risk factor associated with HUA, the authors should add urolithiasis in the introduction. Studies are showing the relationship between uric acid-metabolic syndrome-HUA.

I also believe that the authors should look at the articles on HUA ghrelin and adiponectin - because their results are interesting in the context of metabolic syndrome and they could refer to this in the discussion.

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