Peer Review History

Original SubmissionFebruary 6, 2024
Decision Letter - Melissa Orlandin Premaor, Editor

PONE-D-24-04602Pharmacological prevention of bone loss and fractures following solid organ transplantations: Protocol for a systematic review and network meta-analysisPLOS ONE

Dear Dr. Deng,

Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

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We look forward to receiving your revised manuscript.

Kind regards,

Melissa Orlandin Premaor, M.D., Ph.D

Academic Editor

PLOS ONE

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Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. Does the manuscript provide a valid rationale for the proposed study, with clearly identified and justified research questions?

The research question outlined is expected to address a valid academic problem or topic and contribute to the base of knowledge in the field.

Reviewer #1: Yes

Reviewer #2: Yes

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2. Is the protocol technically sound and planned in a manner that will lead to a meaningful outcome and allow testing the stated hypotheses?

The manuscript should describe the methods in sufficient detail to prevent undisclosed flexibility in the experimental procedure or analysis pipeline, including sufficient outcome-neutral conditions (e.g. necessary controls, absence of floor or ceiling effects) to test the proposed hypotheses and a statistical power analysis where applicable. As there may be aspects of the methodology and analysis which can only be refined once the work is undertaken, authors should outline potential assumptions and explicitly describe what aspects of the proposed analyses, if any, are exploratory.

Reviewer #1: Yes

Reviewer #2: Yes

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3. Is the methodology feasible and described in sufficient detail to allow the work to be replicable?

Descriptions of methods and materials in the protocol should be reported in sufficient detail for another researcher to reproduce all experiments and analyses. The protocol should describe the appropriate controls, sample size calculations, and replication needed to ensure that the data are robust and reproducible.

Reviewer #1: Yes

Reviewer #2: Yes

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4. Have the authors described where all data underlying the findings will be made available when the study is complete?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception, at the time of publication. The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: No

Reviewer #2: No

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5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

Reviewer #2: Yes

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6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above and, if applicable, provide comments about issues authors must address before this protocol can be accepted for publication. You may also include additional comments for the author, including concerns about research or publication ethics.

You may also provide optional suggestions and comments to authors that they might find helpful in planning their study.

(Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: How do you plan to address potential confounding factors in your study, such as differences in patient demographics, comorbidities, and medication histories across the included trials?

Could you elaborate on the rationale behind your choice of outcome measures, particularly in terms of their clinical relevance and sensitivity to detecting differences between treatment groups?

How will your study account for potential changes in clinical practice and the availability of new evidence during the analysis phase?

In your discussion, you mentioned the importance of incorporating Chinese RCTs into your analysis. Could you discuss any challenges you anticipate in accessing and interpreting data from these studies, particularly in terms of language barriers and cultural differences in clinical practice?

Could you discuss the potential limitations of your study?

The study protocol does not explicitly mention where all data underlying the findings will be made available when the study is complete. To ensure transparency and facilitate reproducibility, it would be advisable for the authors to explicitly state their plans for data sharing and accessibility in the final publication or in subsequent updates to the study protocol.

Reviewer #2: Minor suggestions:

- It is preferable to mention which are your primary outcome(s) and which ones are your secondary outcomes.

- There is no mention of how articles published in languages other than English will be handled. This is particularly relevant for your study since you are searching a Chinese database.

- I suggest the addition of network graphs to visualize the overall structure of the comparisons in your network.

- I am not familiar with this field of research, but I am wondering if treatment retention would be important information to extract and report.

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Reviewer #1: Yes: Daniela A. Rodrigues

Reviewer #2: No

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Revision 1

Please see the uploaded "Response to Reviewer Comment" document.

Attachments
Attachment
Submitted filename: Response to Reviewers.docx
Decision Letter - Melissa Orlandin Premaor, Editor

Pharmacological prevention of bone loss and fractures following solid organ transplantations: Protocol for a systematic review and network meta-analysis

PONE-D-24-04602R1

Dear Dr. Deng,

We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements.

Within one week, you’ll receive an e-mail detailing the required amendments. When these have been addressed, you’ll receive a formal acceptance letter and your manuscript will be scheduled for publication.

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Kind regards,

Melissa Orlandin Premaor, M.D., Ph.D

Academic Editor

PLOS ONE

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