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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Pharmacol.</journal-id>
<journal-title>Frontiers in Pharmacology</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Pharmacol.</abbrev-journal-title>
<issn pub-type="epub">1663-9812</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">1622974</article-id>
<article-id pub-id-type="doi">10.3389/fphar.2025.1622974</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Pharmacology</subject>
<subj-group>
<subject>Review</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Efficacy of platelet-rich plasma injection with percutaneous endoscopic lumbar discectomy for lumbar disc herniation: a systematic review and meta-analysis</article-title>
<alt-title alt-title-type="left-running-head">Zhang et al.</alt-title>
<alt-title alt-title-type="right-running-head">
<ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fphar.2025.1622974">10.3389/fphar.2025.1622974</ext-link>
</alt-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Zhang</surname>
<given-names>Yu</given-names>
</name>
<xref ref-type="author-notes" rid="fn1">
<sup>&#x2020;</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/2270072/overview"/>
<role content-type="https://credit.niso.org/contributor-roles/Writing - review &#x26; editing/"/>
<role content-type="https://credit.niso.org/contributor-roles/writing-original-draft/"/>
<role content-type="https://credit.niso.org/contributor-roles/data-curation/"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Ju</surname>
<given-names>Jidong</given-names>
</name>
<uri xlink:href="https://loop.frontiersin.org/people/3055951/overview"/>
<role content-type="https://credit.niso.org/contributor-roles/conceptualization/"/>
<role content-type="https://credit.niso.org/contributor-roles/writing-original-draft/"/>
<role content-type="https://credit.niso.org/contributor-roles/software/"/>
<role content-type="https://credit.niso.org/contributor-roles/data-curation/"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Wu</surname>
<given-names>Jinchun</given-names>
</name>
<xref ref-type="corresp" rid="c001">&#x2a;</xref>
<xref ref-type="author-notes" rid="fn1">
<sup>&#x2020;</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/3055611/overview"/>
<role content-type="https://credit.niso.org/contributor-roles/conceptualization/"/>
<role content-type="https://credit.niso.org/contributor-roles/Writing - review &#x26; editing/"/>
<role content-type="https://credit.niso.org/contributor-roles/formal-analysis/"/>
<role content-type="https://credit.niso.org/contributor-roles/data-curation/"/>
</contrib>
</contrib-group>
<aff>
<institution>Department of Orthopaedics, Jingjiang People&#x2019;s Hospital Affiliated to Yangzhou University</institution>, <addr-line>Taizhou</addr-line>, <addr-line>Jiangsu</addr-line>, <country>China</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>
<bold>Edited by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/1126158/overview">Jinlong Ma</ext-link>, Shandong Second Medical University, China</p>
</fn>
<fn fn-type="edited-by">
<p>
<bold>Reviewed by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/770300/overview">Alexandros Moschovas</ext-link>, University Hospital Jena, Germany</p>
<p>
<ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/1678293/overview">Sherwan Hamawandi</ext-link>, Hawler Medical University, Iraq</p>
</fn>
<corresp id="c001">&#x2a;Correspondence: Jinchun Wu, <email>13961032255@yzu.edu.cn</email>
</corresp>
<fn fn-type="other" id="fn1">
<label>
<sup>&#x2020;</sup>
</label>
<p>
<bold>ORCID:</bold> Yu Zhang, <ext-link ext-link-type="uri" xlink:href="https://orcid.org/0000-0003-0397-8955">orcid.org/0000-0003-0397-8955</ext-link>; Jinchun Wu, <ext-link ext-link-type="uri" xlink:href="https://orcid.org/0009-0006-4646-5374">orcid.org/0009-0006-4646-5374</ext-link>
</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>03</day>
<month>09</month>
<year>2025</year>
</pub-date>
<pub-date pub-type="collection">
<year>2025</year>
</pub-date>
<volume>16</volume>
<elocation-id>1622974</elocation-id>
<history>
<date date-type="received">
<day>05</day>
<month>05</month>
<year>2025</year>
</date>
<date date-type="accepted">
<day>15</day>
<month>08</month>
<year>2025</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2025 Zhang, Ju and Wu.</copyright-statement>
<copyright-year>2025</copyright-year>
<copyright-holder>Zhang, Ju and Wu</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>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.</p>
</license>
</permissions>
<abstract>
<sec>
<title>Objective</title>
<p>Our aim was to compare the efficacy of percutaneous endoscopic lumbar discectomy (PELD) with or without platelet-rich plasma (PRP) injections for the treatment of lumbar disc herniation (LDH).</p>
</sec>
<sec>
<title>Methods</title>
<p>Literature was searched in six databases from inception to 2 May 2025. Meta-analysis was performed using stata17 software.</p>
</sec>
<sec>
<title>Results</title>
<p>Eight studies were included, comprising a total of 717 patients (349 in the treatment group and 368 in the control group). At the final follow-up, the treatment group significantly provided lower visual analogue scale, intervertebral disc protrusion, recurrence rates, Oswestry disability index and higher intervertebral disc height, Japanese Orthopaedic Association scores, spinal canal cross-sectional area and ratio value of disc grey scale, compared to the control group (<italic>p</italic> &#x3c; 0.05).</p>
</sec>
<sec>
<title>Conclusion</title>
<p>Our findings indicate that for the treatment of LDH, PELD combined with PRP injection markedly enhances clinical efficacy while reducing recurrence rates compared to PELD alone. Moving forward, larger multicenter randomized controlled trials with extended follow-up periods are necessary to confirm the long-term efficacy and safety of this combination therapy.</p>
</sec>
<sec>
<title>Systematic Review Registration</title>
<p>Identifier CRD420251044871.</p>
</sec>
</abstract>
<kwd-group>
<kwd>percutaneous endoscopic lumbar discectomy</kwd>
<kwd>platelet-rich plasma injection</kwd>
<kwd>lumbar disc herniation</kwd>
<kwd>efficacy</kwd>
<kwd>meta-analysis</kwd>
</kwd-group>
<counts>
<page-count count="11"/>
</counts>
</article-meta>
</front>
<body>
<sec id="s1">
<title>Introduction</title>
<p>Lumbar disc herniation (LDH) was a widespread and prevalent spine disorder among medical clinics, which seriously affected people&#x2019;s normal work and life, and imposed a heavy burden on global health and socio-economics (<xref ref-type="bibr" rid="B19">Kong et al., 2020</xref>; <xref ref-type="bibr" rid="B7">Chen et al., 2024</xref>; <xref ref-type="bibr" rid="B39">Yang et al., 2024</xref>). LDH was mainly manifested as nerve root pains in the lower legs, sensory disturbances of skin around the distribution of the nerve roots, and limitation of limb movement (<xref ref-type="bibr" rid="B13">Huang et al., 2025</xref>; <xref ref-type="bibr" rid="B15">Jin et al., 2025</xref>). Effective treatments for LDH mainly included conservative and surgical treatments. For patients with incipient LDH, conservative treatments such as medication and physical function exercises were often preferred (<xref ref-type="bibr" rid="B9">Du et al., 2025</xref>; <xref ref-type="bibr" rid="B4">Brotis et al., 2025a</xref>; <xref ref-type="bibr" rid="B5">Brotis et al., 2025b</xref>). 90% of LDH patients could have their symptoms relieved after conservative treatments. However, surgical intervention was required when conservative treatment was ineffective or when neurological function was further aggravated (<xref ref-type="bibr" rid="B28">Mendieta et al., 2025</xref>; <xref ref-type="bibr" rid="B36">Wang et al., 2025</xref>).</p>
<p>Surgical treatment included minimally invasive and traditional open surgery. Conventional open operation was the classical procedure in treating LDH. However, it required extensive stripping of paraspinal muscle and large-scale resection of vertebral plate and facet joints, and resulted in complications such as spinal instability and chronic pain after surgery (<xref ref-type="bibr" rid="B2">Berg et al., 2024</xref>). Recently, thanks to the advancement of minimally invasive technology, spinal endoscopy had gradually become the mainstream clinical treatment of lumbar degenerative diseases for the merits of low trauma, fast rehabilitation and short hospital stay (<xref ref-type="bibr" rid="B37">Xiao et al., 2025</xref>; <xref ref-type="bibr" rid="B18">Ke et al., 2025</xref>; <xref ref-type="bibr" rid="B6">Cai et al., 2025</xref>). At present, percutaneous endoscopic lumbar discectomy (PELD) had been widespread applied for LDH management and obtained satisfactory efficacy. Proper resection of the intervertebral disc could alleviate the pains, but it would inevitably damage the structural integrity of discs and aggravate disc degeneration, and at the same time, the damaged annulus fibrosus would increase the chance of recurrence (<xref ref-type="bibr" rid="B20">Li and Wang, 2025</xref>; <xref ref-type="bibr" rid="B42">Zhao et al., 2025</xref>). Neither conservative nor surgical treatment could fundamentally address the underlying disc degeneration process in LDH. As a consequence, the enhancement of intervertebral disc reconstruction following discectomy was a key issue to improve the operative prognosis. Developments in regenerative medicine promoted the progress of experiments intended to restore and reconstruct healthy intervertebral discs, in particular growth factor therapies, cellular therapies and genetic therapies (<xref ref-type="bibr" rid="B11">Haro et al., 2025</xref>; <xref ref-type="bibr" rid="B1">Anitua et al., 2025</xref>).</p>
<p>As a biological therapy with good biosafety, simple preparation and easy source, platelet-rich plasma (PRP) had been shown to promote intervertebral disc cell proliferation and extracellular matrix synthesis, downregulate the expression of inflammatory factors, and inhibit apoptosis, which was expected to slow down or even reverse the pathological process of intervertebral disc degeneration (<xref ref-type="bibr" rid="B24">Lian et al., 2025</xref>; <xref ref-type="bibr" rid="B41">Zhang et al., 2024</xref>; <xref ref-type="bibr" rid="B33">Tao et al., 2024</xref>). Currently, PRP was widely used in the treatment of lumbar disc diseases and could achieve satisfactory efficacy (<xref ref-type="bibr" rid="B17">Kawabata et al., 2024</xref>; <xref ref-type="bibr" rid="B31">Singh et al., 2023</xref>). Minimally invasive spinal endoscopic removal of herniated intervertebral tissues could alleviate the symptoms of LDH patients, and PRP promoted the repair and regeneration of intervertebral disc tissues and restored the biomechanical function of the intervertebral discs, and the combination of the two techniques could play the effect of &#x201c;1 &#x2b; 1 &#x3e; 2&#x201d;.</p>
<p>PRP injection for treating low back pain <italic>in vitro</italic> had achieved encouraging outcomes. However, there was a paucity of evidence regarding the efficacy and security of PELD combined with PRP in treating LDH. The aim of this meta-analysis was to comprehensively evaluate the effectiveness and security of intraoperative PRP injections during PELD and to determine whether PRP injections might achieve favorable outcomes, enhance disc remodeling and reduce recurrence.</p>
</sec>
<sec sec-type="methods" id="s2">
<title>Methods</title>
<p>This review was carried out according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement (<xref ref-type="bibr" rid="B30">Page et al., 2021</xref>).</p>
<sec id="s2-1">
<title>Eligibility</title>
<sec id="s2-1-1">
<title>Inclusion criteria</title>
<p>Participants: patients with a clinically and radiologically confirmed diagnosis of LDH requiring surgery.</p>
<p>Intervention: PELD combined with PRP as the treatment group.</p>
<p>Comparison: PELD only as the control group.</p>
<p>Outcomes: visual analogue score (VAS) for back pain and leg pain, intervertebral disc height (IDH), intervertebral disc protrusion (IDP), Oswestry disability index (ODI), Japanese Orthopaedic Association (JOA) score, spinal canal cross-sectional area (SCSA), recurrence, ratio value of disc grey scales (RVG). Studies included at least one of the above outcomes. The definitions and measurements of the outcome indicators were detailed in the <xref ref-type="sec" rid="s13">Supplementary File 1</xref>.</p>
<p>Study design: observational studies, randomized controlled trials. Follow-up time was at least 1 year.</p>
</sec>
<sec id="s2-1-2">
<title>Exclusion criteria</title>
<p>
<list list-type="simple">
<list-item>
<p>1. Researches including patients with other lumbar spine conditions (e.g., fractures, infections, tumors) or with documented lumbar spine surgery.</p>
</list-item>
<list-item>
<p>2. Duplicate reports, case reports, reviews, meta-analyses, animal studies, biomechanical studies, letters, and conference abstracts.</p>
</list-item>
<list-item>
<p>3. Incomplete or unanalyzable raw information.</p>
</list-item>
</list>
</p>
</sec>
</sec>
<sec id="s2-2">
<title>Search strategy</title>
<p>A comprehensive literature search was carried out in 6 databases such as PubMed, Embase, Web of Science, Cochrane Library, Wanfang and China National Knowledge Infrastructure from the beginning of databases to 2 May 2025. The search formula was as follows (platelet rich plasma) AND (discectomy). Only English and Chinese publications were included.</p>
</sec>
<sec id="s2-3">
<title>Data extraction</title>
<p>Two investigators separately extracted the following data from these eligible papers.<list list-type="simple">
<list-item>
<p>1. Study information: author name, publication year, country and study type.</p>
</list-item>
<list-item>
<p>2. Baseline characteristics: sample size, age, length of observation.</p>
</list-item>
<list-item>
<p>3. Endpoints to be investigated.</p>
</list-item>
</list>
</p>
</sec>
<sec id="s2-4">
<title>Quality evaluation</title>
<p>Newcastle-Ottawa Scale (NOS) was used to determine the quality of observational researches. The total score was 9, with &#x2265;6 considered high quality.</p>
</sec>
<sec id="s2-5">
<title>Statistical analyses</title>
<p>Meta-analyses were performed using Stata 17.0. Heterogeneity of included researches was determined via I<sup>2</sup> statistic. Effect sizes were pooled using a random-effects model when I<sup>2</sup> &#x3e;50% indicated significant heterogeneity between included studies. For continuous outcomes, effect sizes were expressed as weighted mean difference (WMD) and 95% confidence intervals (CI). For dichotomous outcomes, effect sizes were estimated as odds ratios (ORs) and 95% CIs. Sensitivity analyses were performed by stepwise deletion of each individual trial to determine the robustness of the combined results. Egger test was employed to objectively investigate publication bias. <italic>P</italic> &#x3c; 0.05 was used to demonstrate statistical significance.</p>
</sec>
</sec>
<sec sec-type="results" id="s3">
<title>Results</title>
<sec id="s3-1">
<title>Search process and results</title>
<p>Initially, 70 relevant articles were selected through a comprehensive review of 6 electronic databases. Ultimately, eight papers were considered for inclusion in our analysis (<xref ref-type="bibr" rid="B14">Jiang et al., 2022</xref>; <xref ref-type="bibr" rid="B22">Li et al., 2024a</xref>; <xref ref-type="bibr" rid="B40">Zhang et al., 2023</xref>; <xref ref-type="bibr" rid="B8">Du et al., 2020</xref>; <xref ref-type="bibr" rid="B23">Li et al., 2024b</xref>; <xref ref-type="bibr" rid="B25">Lin et al., 2022</xref>; <xref ref-type="bibr" rid="B32">Su, 2024</xref>; <xref ref-type="bibr" rid="B34">Tusheng et al., 2024</xref>) (<xref ref-type="fig" rid="F1">Figure 1</xref>).</p>
<fig id="F1" position="float">
<label>FIGURE 1</label>
<caption>
<p>Flow chart of literature search.</p>
</caption>
<graphic xlink:href="fphar-16-1622974-g001.tif">
<alt-text content-type="machine-generated">>Flowchart illustrating the process of study identification for meta-analysis. Starting with 70 records from databases, 30 duplicates were removed. After screening 40 records, 10 were excluded. Of 30 reports sought, none were not retrieved, but 22 were excluded, leaving 8 studies included in the meta-analysis.</alt-text>
</graphic>
</fig>
</sec>
<sec id="s3-2">
<title>Study characteristics</title>
<p>All eligible studies were observational and conducted in China. A total of 717 participants received LDH between 2020 and 2024, including 349 cases in the treatment group and 368 cases in the control group (<xref ref-type="table" rid="T1">Table 1</xref>).</p>
<table-wrap id="T1" position="float">
<label>TABLE 1</label>
<caption>
<p>Study characteristics.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th rowspan="2" align="left">Author</th>
<th rowspan="2" align="left">Publication year</th>
<th rowspan="2" align="left">Country</th>
<th rowspan="2" align="left">Study design</th>
<th colspan="2" align="left">Sample size</th>
<th colspan="2" align="left">Age (years)</th>
<th colspan="2" align="left">Follow-up (months)</th>
</tr>
<tr>
<th align="left">Treatment</th>
<th align="left">Control</th>
<th align="left">Treatment</th>
<th align="left">Control</th>
<th align="left">Treatment</th>
<th align="left">Control</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">Du</td>
<td align="left">2020</td>
<td align="left">China</td>
<td align="left">OS</td>
<td align="left">20</td>
<td align="left">20</td>
<td align="left">47.80 &#xb1; 13.46</td>
<td align="left">45.85 &#xb1; 10.45</td>
<td align="left">24.2 &#xb1; 1.9</td>
<td align="left">24.2 &#xb1; 1.9</td>
</tr>
<tr>
<td align="left">Jiang</td>
<td align="left">2022</td>
<td align="left">China</td>
<td align="left">OS</td>
<td align="left">51</td>
<td align="left">57</td>
<td align="left">48.1 &#xb1; 10.25</td>
<td align="left">45.9 &#xb1; 9.83</td>
<td align="left">12</td>
<td align="left">12</td>
</tr>
<tr>
<td align="left">Lin</td>
<td align="left">2022</td>
<td align="left">China</td>
<td align="left">OS</td>
<td align="left">36</td>
<td align="left">37</td>
<td align="left">48.36 &#xb1; 9.53</td>
<td align="left">49.12 &#xb1; 8.72</td>
<td align="left">15.37 &#xb1; 1.92</td>
<td align="left">15.37 &#xb1; 1.92</td>
</tr>
<tr>
<td align="left">Li</td>
<td align="left">2023</td>
<td align="left">China</td>
<td align="left">OS</td>
<td align="left">38</td>
<td align="left">47</td>
<td align="left">43.84 &#xb1; 13.15</td>
<td align="left">41.79 &#xb1; 12.05</td>
<td align="left">28.16 &#xb1; 2.59</td>
<td align="left">27.96 &#xb1; 2.40</td>
</tr>
<tr>
<td align="left">Zhang</td>
<td align="left">2023</td>
<td align="left">China</td>
<td align="left">OS</td>
<td align="left">50</td>
<td align="left">48</td>
<td align="left">41.5 &#xb1; 9.8</td>
<td align="left">45.8 &#xb1; 11.0</td>
<td align="left">18</td>
<td align="left">18</td>
</tr>
<tr>
<td align="left">Li</td>
<td align="left">2024</td>
<td align="left">China</td>
<td align="left">OS</td>
<td align="left">75</td>
<td align="left">80</td>
<td align="left">43.61 &#xb1; 11.72</td>
<td align="left">44.25 &#xb1; 11.56</td>
<td align="left">12</td>
<td align="left">12</td>
</tr>
<tr>
<td align="left">Li</td>
<td align="left">2024</td>
<td align="left">China</td>
<td align="left">OS</td>
<td align="left">30</td>
<td align="left">30</td>
<td align="left">37.1 &#xb1; 11.0</td>
<td align="left">36.9 &#xb1; 10.7</td>
<td align="left">27.2 &#xb1; 2.0</td>
<td align="left">27.2 &#xb1; 2.0</td>
</tr>
<tr>
<td align="left">Su</td>
<td align="left">2024</td>
<td align="left">China</td>
<td align="left">OS</td>
<td align="left">49</td>
<td align="left">49</td>
<td align="left">46.18 &#xb1; 8.92</td>
<td align="left">46.85 &#xb1; 9.28</td>
<td align="left">12</td>
<td align="left">12</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>OS, observational study.</p>
</fn>
</table-wrap-foot>
</table-wrap>
</sec>
<sec id="s3-3">
<title>Quality assessment</title>
<p>Information on the quality evaluation was shown in <xref ref-type="table" rid="T2">Table 2</xref>. Each article scored at least 7 and was categorized as high quality.</p>
<table-wrap id="T2" position="float">
<label>TABLE 2</label>
<caption>
<p>Newcastle-Ottawa Scale of included observational studies.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="left">Study</th>
<th align="center">Selection</th>
<th align="center">Comparability</th>
<th align="center">Outcome</th>
<th align="center">Total score</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">Du 2020</td>
<td align="center">3</td>
<td align="center">1</td>
<td align="center">3</td>
<td align="center">7</td>
</tr>
<tr>
<td align="left">Jiang 2022</td>
<td align="center">4</td>
<td align="center">1</td>
<td align="center">3</td>
<td align="center">8</td>
</tr>
<tr>
<td align="left">Lin 2022</td>
<td align="center">4</td>
<td align="center">1</td>
<td align="center">3</td>
<td align="center">8</td>
</tr>
<tr>
<td align="left">Li 2023</td>
<td align="center">4</td>
<td align="center">1</td>
<td align="center">3</td>
<td align="center">8</td>
</tr>
<tr>
<td align="left">Zhang 2023</td>
<td align="center">4</td>
<td align="center">1</td>
<td align="center">3</td>
<td align="center">8</td>
</tr>
<tr>
<td align="left">Li 2024A</td>
<td align="center">4</td>
<td align="center">1</td>
<td align="center">3</td>
<td align="center">8</td>
</tr>
<tr>
<td align="left">Li 2024B</td>
<td align="center">4</td>
<td align="center">1</td>
<td align="center">3</td>
<td align="center">8</td>
</tr>
<tr>
<td align="left">Su 2024</td>
<td align="center">3</td>
<td align="center">1</td>
<td align="center">3</td>
<td align="center">7</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
<sec id="s3-4">
<title>Meta-analysis results</title>
<sec id="s3-4-1">
<title>VAS</title>
<p>Eight studies reported VAS for back pain and leg pain separately, including 717 patients (349 in the treatment group and 368 in the control group). Ultimately, the results of the meta-analysis showed that at the final follow-up, the treatment group had significantly less VAS for back pain [WMD &#x3d; &#x2212;0.32, 95% CI (&#x2212;0.49, &#x2212;0.15), <italic>p</italic> &#x3c; 0.01] (<xref ref-type="fig" rid="F2">Figure 2</xref>) and VAS for leg pain [WMD &#x3d; &#x2212;0.29, 95% CI (&#x2212;0.50, &#x2212;0.09), <italic>p</italic> &#x3c; 0.01] (<xref ref-type="fig" rid="F3">Figure 3</xref>) than the control group (<xref ref-type="table" rid="T3">Table 3</xref>).</p>
<fig id="F2" position="float">
<label>FIGURE 2</label>
<caption>
<p>Forest plot of visual analogue score for back pain.</p>
</caption>
<graphic xlink:href="fphar-16-1622974-g002.tif">
<alt-text content-type="machine-generated">Forest plot showing mean differences with 95% confidence intervals for multiple studies comparing treatment and control groups. Studies include Du 2020, Jiang 2022, Lin 2022, and others. The mean differences range from negative to positive values, with varying weights. The overall effect size is depicted as a diamond. Heterogeneity statistics are provided, including I-squared at 60.88%. The random-effects model is used.</alt-text>
</graphic>
</fig>
<fig id="F3" position="float">
<label>FIGURE 3</label>
<caption>
<p>Forest plot of visual analogue score for leg pain.</p>
</caption>
<graphic xlink:href="fphar-16-1622974-g003.tif">
<alt-text content-type="machine-generated">Forest plot showing a meta-analysis of eight studies comparing treatment and control groups. Each study is represented by a square, and horizontal lines show the 95% confidence intervals of the mean difference. The size of the squares indicates the weight of each study. Most studies favor the control group, with one study overlapping zero. The pooled estimate is represented by a diamond, indicating an overall mean difference of &#x2010;0.29, with a 95% confidence interval from &#x2010;0.50 to &#x2010;0.09. Heterogeneity metrics indicate variability across studies.</alt-text>
</graphic>
</fig>
<table-wrap id="T3" position="float">
<label>TABLE 3</label>
<caption>
<p>Findings of meta-analysis.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th rowspan="2" align="left">Outcomes</th>
<th align="center">Study</th>
<th align="center">Effect size</th>
<th colspan="2" align="center">95% CI</th>
<th rowspan="2" align="center">P-value</th>
<th colspan="2" align="center">Heterogeneity</th>
<th align="center">Effects</th>
<th align="center">Egger test</th>
</tr>
<tr>
<th align="center">Size</th>
<th align="center">WMD/OR</th>
<th align="center">Lower limit</th>
<th align="center">Upper limit</th>
<th align="center">I<sup>2</sup> (%)</th>
<th align="center">
<italic>P</italic>-value</th>
<th align="center">Model</th>
<th align="center">
<italic>P</italic>-value</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">VAS for back pain</td>
<td align="center">8</td>
<td align="center">&#x2212;0.32</td>
<td align="center">&#x2212;0.49</td>
<td align="center">&#x2212;0.15</td>
<td align="center">&#x3c;0.01</td>
<td align="center">60.88</td>
<td align="center">0.01</td>
<td align="center">Random</td>
<td align="center">0.28</td>
</tr>
<tr>
<td align="left">VAS for leg pain</td>
<td align="center">8</td>
<td align="center">&#x2212;0.29</td>
<td align="center">&#x2212;0.50</td>
<td align="center">&#x2212;0.09</td>
<td align="center">&#x3c;0.01</td>
<td align="center">67.68</td>
<td align="center">&#x3c;0.01</td>
<td align="center">Random</td>
<td align="center">0.67</td>
</tr>
<tr>
<td align="left">JOA scores</td>
<td align="center">5</td>
<td align="center">1.82</td>
<td align="center">0.09</td>
<td align="center">3.55</td>
<td align="center">0.04</td>
<td align="center">93.20</td>
<td align="center">&#x3c;0.01</td>
<td align="center">Random</td>
<td align="center">0.51</td>
</tr>
<tr>
<td align="left">ODI</td>
<td align="center">8</td>
<td align="center">&#x2212;2.46</td>
<td align="center">&#x2212;4.56</td>
<td align="center">&#x2212;0.36</td>
<td align="center">0.02</td>
<td align="center">90.10</td>
<td align="center">&#x3c;0.01</td>
<td align="center">Random</td>
<td align="center">0.82</td>
</tr>
<tr>
<td align="left">IDH</td>
<td align="center">5</td>
<td align="center">0.73</td>
<td align="center">0.50</td>
<td align="center">0.95</td>
<td align="center">&#x3c;0.01</td>
<td align="center">1.01</td>
<td align="center">0.40</td>
<td align="center">Fixed</td>
<td align="center">0.19</td>
</tr>
<tr>
<td align="left">IDP</td>
<td align="center">2</td>
<td align="center">&#x2212;0.13</td>
<td align="center">&#x2212;0.23</td>
<td align="center">&#x2212;0.04</td>
<td align="center">&#x3c;0.01</td>
<td align="center">47.47</td>
<td align="center">0.17</td>
<td align="center">Fixed</td>
<td align="center">0.17</td>
</tr>
<tr>
<td align="left">SCSA</td>
<td align="center">2</td>
<td align="center">9.85</td>
<td align="center">5.04</td>
<td align="center">14.66</td>
<td align="center">&#x3c;0.01</td>
<td align="center">46.28</td>
<td align="center">0.17</td>
<td align="center">Fixed</td>
<td align="center">0.17</td>
</tr>
<tr>
<td align="left">RVG</td>
<td align="center">3</td>
<td align="center">1.69</td>
<td align="center">0.82</td>
<td align="center">2.56</td>
<td align="center">&#x3c;0.01</td>
<td align="center">0.00</td>
<td align="center">0.37</td>
<td align="center">Fixed</td>
<td align="center">0.16</td>
</tr>
<tr>
<td align="left">Recurrence</td>
<td align="center">4</td>
<td align="center">0.27</td>
<td align="center">0.10</td>
<td align="center">0.70</td>
<td align="center">0.01</td>
<td align="center">0.00</td>
<td align="center">0.92</td>
<td align="center">Fixed</td>
<td align="center">0.91</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>VAS, visual analogue score; IDH, intervertebral disc height; IDP, intervertebral disc protrusion; ODI, oswestry disability index; JOA, japanese orthopaedic association; SCSA, spinal canal cross-sectional area; RVG, ratio value of disc grey scales; WMD, weighted mean difference; CI, confidence intervals; OR, odds ratio.</p>
</fn>
</table-wrap-foot>
</table-wrap>
</sec>
<sec id="s3-4-2">
<title>JOA scores</title>
<p>JOA scores were recorded in five papers, including 438 patients. At the final follow-up, the treatment group provided higher JOA scores than the control group [WMD &#x3d; 1.82, 95% CI (0.09, 3.55), <italic>p</italic> &#x3d; 0.04] (<xref ref-type="fig" rid="F4">Figure 4</xref>).</p>
<fig id="F4" position="float">
<label>FIGURE 4</label>
<caption>
<p>Forest plot of Japanese Orthopaedic Association scores.</p>
</caption>
<graphic xlink:href="fphar-16-1622974-g004.tif">
<alt-text content-type="machine-generated">Forest plot showing mean differences between treatment and control groups across five studies, each with confidence intervals and weight percentages. Overall mean difference is 1.82 with a 95% confidence interval of 0.09 to 3.55. Heterogeneity statistics are displayed, including I-squared at 93.20%. Random-effects REML model is used.</alt-text>
</graphic>
</fig>
</sec>
<sec id="s3-4-3">
<title>ODI</title>
<p>Eight studies analyzed ODI data. At the final follow-up, the treatment group had a significantly smaller ODI than the control group [WMD &#x3d; &#x2212;2.46, 95% CI (&#x2212;4.56, &#x2212;0.36), <italic>p</italic> &#x3d; 0.02] (<xref ref-type="fig" rid="F5">Figure 5</xref>).</p>
<fig id="F5" position="float">
<label>FIGURE 5</label>
<caption>
<p>Forest plot of Oswestry disability index.</p>
</caption>
<graphic xlink:href="fphar-16-1622974-g005.tif">
<alt-text content-type="machine-generated">Forest plot from a meta-analysis showing studies comparing treatment and control groups. The plot displays mean differences with 95% confidence intervals for each study and overall effect. Studies are listed with sample size, mean, standard deviation, mean difference, confidence intervals, and weights. Key statistics: heterogeneity and test results. Visual elements include blue squares for individual studies and a green diamond for the overall effect size, located at &#x2010;2.46 with a confidence interval of &#x2010;4.56 to &#x2010;0.36.</alt-text>
</graphic>
</fig>
</sec>
<sec id="s3-4-4">
<title>IDH</title>
<p>Five publications recorded information on IDH, including 208 in the treatment group and 221 in the control group. At the final follow-up, IDH was significantly greater in the treatment group than in the control group [WMD &#x3d; 0.73, 95% CI (0.50, 0.95), <italic>p</italic> &#x3c; 0.01] (<xref ref-type="fig" rid="F6">Figure 6</xref>).</p>
<fig id="F6" position="float">
<label>FIGURE 6</label>
<caption>
<p>Forest plot of intervertebral disc height.</p>
</caption>
<graphic xlink:href="fphar-16-1622974-g006.tif">
<alt-text content-type="machine-generated">Forest plot showing five studies comparing treatment and control groups. The studies listed are Du 2020, Jiang 2022, Li 2023, Zhang 2023, and Su 2024. Each study provides mean, standard deviation, mean difference with 95% confidence interval, and weight percentage. The overall effect is 0.73 with 95% confidence interval [0.50, 0.95]. The heterogeneity shown is low with I-squared at 1.01%. A fixed-effects inverse&#x2010;variance model is used.</alt-text>
</graphic>
</fig>
</sec>
<sec id="s3-4-5">
<title>IDP</title>
<p>A total of 263 participants in 2 studies were evaluated for IDP data. At the final follow-up, the control group showed more pronounced disc protrusion than the treatment group [WMD &#x3d; &#x2212;0.13, 95% CI (&#x2212;0.23, &#x2212;0.04), <italic>p</italic> &#x3c; 0.01] (<xref ref-type="fig" rid="F7">Figure 7</xref>).</p>
<fig id="F7" position="float">
<label>FIGURE 7</label>
<caption>
<p>Forest plot of intervertebral disc protrusion.</p>
</caption>
<graphic xlink:href="fphar-16-1622974-g007.tif">
<alt-text content-type="machine-generated">Forest plot comparing treatment and control groups in two studies, Jiang 2022 and Li 2024A. The mean difference with ninety-five percent confidence intervals is shown, with Jiang 2022 at negative 0.42 and Li 2024A at negative 0.12. Overall mean difference is negative 0.13. Heterogeneity is forty-seven point four seven percent. Fixed&#x2010;effects inverse-variance model is used.</alt-text>
</graphic>
</fig>
</sec>
<sec id="s3-4-6">
<title>SCSA</title>
<p>Two research studies contained information on SCSA, consisting of 126 in the treatment group and 137 in the control group. At the final follow-up, the treatment group obtained more SCSA than the control group [WMD &#x3d; 9.85, 95% CI (5.04, 14.66), <italic>p</italic> &#x3c; 0.01] (<xref ref-type="fig" rid="F8">Figure 8</xref>).</p>
<fig id="F8" position="float">
<label>FIGURE 8</label>
<caption>
<p>Forest plot of spinal canal cross-sectional area.</p>
</caption>
<graphic xlink:href="fphar-16-1622974-g008.tif">
<alt-text content-type="machine-generated">Forest plot comparing treatment and control groups from two studies, Jiang 2022 and Li 2024A. Treatment shows higher mean differences with 95% confidence intervals: 17.80 for Jiang 2022 and 8.44 for Li 2024A. Weights are 15.07% and 84.93%. Overall mean difference is 9.85. Heterogeneity measures include I-squared at 46.28%. Fixed&#x2010;effects inverse-variance model used.</alt-text>
</graphic>
</fig>
</sec>
<sec id="s3-4-7">
<title>RVG</title>
<p>Three studies recorded RVG. At the last follow-up, the treatment group had a significantly higher RVG than the control group [WMD &#x3d; 1.69, 95% CI (0.82, 2.56), <italic>p</italic> &#x3c; 0.01] (<xref ref-type="fig" rid="F9">Figure 9</xref>).</p>
<fig id="F9" position="float">
<label>FIGURE 9</label>
<caption>
<p>Forest plot of ratio value of disc grey scales.</p>
</caption>
<graphic xlink:href="fphar-16-1622974-g009.tif">
<alt-text content-type="machine-generated">Forest plot showing three studies (Li 2023, Li 2024A, Li 2024B) comparing treatment and control groups. Mean differences with 95% confidence intervals are displayed as horizontal lines with squares, and an overall pooled effect is shown as a diamond. Heterogeneity I&#x2010;squared is 0.00 percent. The fixed-effects inverse-variance model is used.</alt-text>
</graphic>
</fig>
</sec>
</sec>
<sec id="s3-5">
<title>Recurrence</title>
<p>Recurrence information was recorded in four papers comprising 446 patients (treatment group 214, control group 232). At the final follow-up, the recurrence rate was significantly lower in the treatment group than in the control group [OR &#x3d; 0.27, 95% CI (0.10, 0.70), <italic>p</italic> &#x3d; 0.01] (<xref ref-type="fig" rid="F10">Figure 10</xref>).</p>
<fig id="F10" position="float">
<label>FIGURE 10</label>
<caption>
<p>Forest plot of recurrence rate.</p>
</caption>
<graphic xlink:href="fphar-16-1622974-g010.tif">
<alt-text content-type="machine-generated">Forest plot showing risk ratios with 95% confidence intervals from studies Jiang 2022, Li 2023, Zhang 2023, and Li 2024A. Individual risk ratios range from 0.15 to 0.41. The combined overall risk ratio is 0.27 with a confidence interval of 0.10 to 0.70. Weights range from 13.86% to 35.00%. Heterogeneity measures include I&#x2010;squared at 0.00%, H&#x2010;squared at 1.00%. The statistical tests show p-values of 0.92 and 0.01 respectively.</alt-text>
</graphic>
</fig>
</sec>
<sec id="s3-6">
<title>Sensitivity analyses</title>
<p>Sensitivity analyses showed that the results of meta-analyses were robust for all outcome indicators except JOA scores and ODI (<xref ref-type="sec" rid="s13">Supplementary File 2</xref>).</p>
</sec>
<sec id="s3-7">
<title>Publication bias</title>
<p>Egger test was used to detect publication bias, and the findings demonstrated no publication bias within our study (<italic>p</italic> &#x3e; 0.05) (<xref ref-type="sec" rid="s13">Supplementary File 3</xref>).</p>
</sec>
</sec>
<sec sec-type="discussion" id="s4">
<title>Discussion</title>
<p>In recent years, the incidence of LDH increased with age, which seriously affected people&#x2019;s health and quality of life. Surgical intervention was a necessary treatment for patients with LDH who could not achieve satisfactory results with conservative treatment. Conventional open operation was the classical therapy in treating LDH, however, it required extensive resection of the vertebral laminas and facet joints, as well as extensive stripping of the paraspinal muscle, which could easily induce complications such as lumbar postoperative failure syndrome. With the popularity of minimally invasive concept, minimally invasive spinal endoscopy became one of the mainstream surgical procedures for the treatment of LDH. PELD was widespread applied for treating LDH, and could achieve satisfactory clinical efficacy. However, minimally invasive spinal endoscopy could not essentially delay disc degeneration and could lead to further aggravation of disc degeneration after surgery. In addition, the non-vascular nature of the intervertebral disc made the repair ability after disc degeneration poor. Therefore, how to slow down disc degeneration and enhance disc repair and regeneration was a key clinical problem that needed to be solved urgently.</p>
<p>With many scholars exploring the mechanism of intervertebral disc degeneration, PRP was gaining more and more attention as a new, green regenerative therapy. PRP was a platelet concentrate obtained from fresh whole blood after centrifugal separation, and platelets could release a variety of growth factors after activation, such as platelet-derived growth factor, vascular endothelial growth factor, insulin-like growth factor, transforming growth factor &#x3b2;, epidermal growth factor and so on, which had been confirmed to have the effects of promoting the remodeling and regeneration of intervertebral discs, angiogenesis, anti-inflammation and so on (<xref ref-type="bibr" rid="B26">Luan et al., 2025</xref>). At present, PRP had been extensively utilized for treating lumbar diseases, achieving favorable clinical efficacy (<xref ref-type="bibr" rid="B41">Zhang et al., 2024</xref>).</p>
<p>To date, there were few studies about PRP injections combined with PELD for the treatment of LDH. Nevertheless, some papers reported clinical findings after intradiscal PRP injection for treating lumbar diseases (<xref ref-type="bibr" rid="B41">Zhang et al., 2024</xref>; <xref ref-type="bibr" rid="B16">Kaux et al., 2024</xref>). A meta-analysis found intradiscal injections led to statistically significant improvements in the VAS, with lower incidence of complications and reinjections (<xref ref-type="bibr" rid="B12">Hirase et al., 2020</xref>). To the best of our knowledge, our study was the first meta-analysis to comprehensively compare the effectiveness of PELD combined with PRP injections for LDH. In this study, we found PELD combined with PRP could provide lower VAS, ODI, IDP, and recurrence rates, and higher JOA scores, IDH, SCSA, and DVG, compared with PELD alone. Our findings suggested that intraoperative PRP injection following PELD might benefit annulus fibrosus repair, delay intervertebral disc degeneration and improve clinical outcomes.</p>
<p>The main principle of PRP in repairing degenerated discs was to inject a high concentration of platelets directly into the disc to initiate a healing cascade. The fibronectin in PRP provided a scaffolding structure for cell proliferation and tissue repair, preventing cell loss while adhering to the annulus fibrosus cells to further seal the annulus fibrosus fracture. Previous animal experiments demonstrated PRP could significantly suppress inflammation mediated by inflammatory mediators and pro-degradative enzymes, thus hindering progressive intervertebral disc degeneration (<xref ref-type="bibr" rid="B33">Tao et al., 2024</xref>; <xref ref-type="bibr" rid="B26">Luan et al., 2025</xref>).</p>
<p>In 2011, Akeda et al. were the first to demonstrate autologous PRP applied within the intervertebral disc was a secure and beneficial biotherapy in treating lumbar degenerative diseases. Since then, PRP had been extensively employed for treating lumbar disc disease and achieved encouraging clinical results. In this study, VAS, ODI and JOA scores of LDH patients treated with PRP improved more significantly, indicating that PRP could help to relieve pain and improve the quality of life. The efficacy of PRP injections seemed to be associated not only with the interaction of local inflammatory factors, but also with the repairs of local damage. Those receiving PRP injections exhibited better performance in pain management, while PRP could reduce postsurgical pain and numbness. We suggested that injecting PRP around a lesion might release numerous factors, which might alleviate inflammation as well as relieve symptom. In our study, there were significant differences regarding ODI between both groups, which could be related to multiple factors released from PRP, playing a role in interference with scar formation surrounding neural tissue. The impact of PRP infiltration on extracellular matrix synthesis, anti-inflammatory mechanisms, analgesia and subchondral bone homeostasis might facilitate intervertebral disc repair. In summary, these might boost endogenous repair mechanisms and enhance recovery.</p>
<p>Discectomy unavoidably led to subsequent disc degeneration. IDH loss was a natural process of intervertebral disc degeneration following discectomy. A previous investigation showed PRP injections prevented the reduction of DH in a rabbit model (<xref ref-type="bibr" rid="B10">Gui et al., 2015</xref>). The results of this previous trial were comparable to our findings. At the last follow-up, LDH patients with PRP injection showed a smaller decrease in IDH, suggesting that PRP was able to delay disc degeneration to some extent.</p>
<p>Residual annulus noted by MRI was prevalent in the early postoperative period following PELD. Variations in DVG and IDP over time suggested the possibility of disc remodeling (<xref ref-type="bibr" rid="B27">Mahatthanatrakul et al., 2019</xref>). In our study, the PRP group had less disc protrusion and greater SCSA and DVG during the follow-up period, suggesting that PRP played an active role in annulus fibrosus remodeling. These changes led to enlargement in spinal canal space and reduction of nerve root compression and irritation, which explained the alleviation of clinical symptom in a different way.</p>
<p>In our study, the incidence of recurrence was significantly less in the treatment group, suggesting PRP could contribute to the prevention of recurrence. Ideal annulus fibrosus remodeling could effectively establish a mechanical barrier to protect against subsequent recurrence of disc protrusion, decrease the appearance of recompression, as well as extending the spinal canal, avoiding the formation of postoperative fibrotic scarring in the spinal canal, and minimizing the release of inflammation factors, thus achieving favorable effects and preventing the incidence of postsurgical pains and numbness. Following proper repair of the annulus fibrosus, the intervertebral disc could be regarded as a sealed area, which prevented the leakage of biological agents and provided the foundation for biologic therapy of the intervertebral disc. Also, homeostasis of discs was the rationale for avoidance of recurrence (<xref ref-type="bibr" rid="B21">Li et al., 2021</xref>).</p>
<p>Meanwhile, the safety of PRP was also a major concern. Because PRP was derived from autologous blood without immune rejection, it had limited potential for infection and allergic reaction (<xref ref-type="bibr" rid="B38">Xie et al., 2020</xref>). It was also reported that PRP had anti-microbial properties, which helped to reduce the risk of infection after surgery (<xref ref-type="bibr" rid="B29">Mohammed and Yu, 2018</xref>). Du et al. reported one patient in the observation group suffered from aggravation of radicular symptom on the next day after treatment, which was considered to be caused by increased disc pressure after the placement of PRP gel microspheres or irritation of the nerve root by a small amount of inflammatory factors such as leukocytes in the PRP, and the symptoms were relieved after symptomatic treatment, and there was no neurological damage such as decreased sensory muscle power in the lower extremities (<xref ref-type="bibr" rid="B8">Du et al., 2020</xref>).</p>
<p>There were still different opinions on the form of PRP to be used. Bhatia et al. injected 5&#xa0;mL of PRP solution into nerve root region around diseased segments by the epidural route, and the follow-up results showed a significant improvement in the patients&#x2019; VAS scores and straight leg raising test within 3 months (<xref ref-type="bibr" rid="B3">Bhatia and Chopra, 2016</xref>). In order to prevent spillage of PRP solution, Vadal&#xe0; et al. designed a new injectable hydrogel composed of PRP, hyaluronic acid and patulinase, and biological tests showed that this preparation improved the cell viability and proliferation of their MSCs (<xref ref-type="bibr" rid="B35">Vadala et al., 2017</xref>). Li et al. reported that PRP injection into the gel capsule enabled the slow release of high concentrations of growth factors in PRP and their sustained action on intervertebral disc cells, which greatly improved the therapeutic effect of PRP in repairing degenerated intervertebral discs (<xref ref-type="bibr" rid="B23">Li et al., 2024b</xref>).</p>
</sec>
<sec id="s5">
<title>Limitations</title>
<p>Our study had several limitations. Firstly, the limited sample size might impact the representativeness of the study results. Secondly, variations in PRP preparation techniques, as well as differences in injection dosage and composition, could introduce bias into the results. Thirdly, all eligible studies were conducted in China, which might impose geographic and healthcare system constraints on generalizability. Fourthly, incomplete reporting of complications in some studies might have led to an underestimation of risk. Finally, the follow-up period was insufficient to comprehensively assess the long-term benefits and risks associated with PRP application. Therefore, future research should aim to extend follow-up duration and increase sample sizes to further validate the long-term efficacy and safety of PRP therapy. Additionally, it is important to note that active components and concentrations of PRP extracted through different methods can vary significantly. Future investigations should focus on determining optimal PRP concentration and injection dosage for promoting intervertebral disc repair, as well as identifying implantation methods and treatment durations that maximize the therapeutic potential of PRP.</p>
</sec>
<sec sec-type="conclusion" id="s6">
<title>Conclusion</title>
<p>Our study demonstrated that compared with PELD alone, PELD combined with PRP significantly reduced VAS scores, ODI, IDP and recurrence rates while increasing JOA scores, IDH, SCSA and DVG. In conclusion, these findings indicate that for the treatment of LDH, PELD combined with PRP injection markedly enhances clinical efficacy while reducing recurrence rates compared to PELD alone. Moving forward, larger multicenter randomized controlled trials with extended follow-up periods are necessary to confirm the long-term efficacy and safety of this combination therapy.</p>
</sec>
</body>
<back>
<sec sec-type="author-contributions" id="s7">
<title>Author contributions</title>
<p>YZ: Writing &#x2013; review and editing, Writing &#x2013; original draft, Data curation. JJ: Conceptualization, Writing &#x2013; original draft, Software, Data curation. JW: Conceptualization, Writing &#x2013; review and editing, Formal Analysis, Data curation.</p>
</sec>
<sec sec-type="funding-information" id="s8">
<title>Funding</title>
<p>The author(s) declare that no financial support was received for the research and/or publication of this article.</p>
</sec>
<sec sec-type="COI-statement" id="s9">
<title>Conflict of interest</title>
<p>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.</p>
</sec>
<sec sec-type="ai-statement" id="s10">
<title>Generative AI statement</title>
<p>The author(s) declare that no Generative AI was used in the creation of this manuscript.</p>
<p>Any alternative text (alt text) provided alongside figures in this article has been generated by Frontiers with the support of artificial intelligence and reasonable efforts have been made to ensure accuracy, including review by the authors wherever possible. If you identify any issues, please contact us.</p>
</sec>
<sec sec-type="disclaimer" id="s11">
<title>Publisher&#x2019;s note</title>
<p>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.</p>
</sec>
<sec sec-type="supplementary-material" id="s12">
<title>Supplementary material</title>
<p>The Supplementary Material for this article can be found online at: <ext-link ext-link-type="uri" xlink:href="https://www.frontiersin.org/articles/10.3389/fphar.2025.1622974/full#supplementary-material">https://www.frontiersin.org/articles/10.3389/fphar.2025.1622974/full&#x23;supplementary-material</ext-link>
</p>
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<supplementary-material xlink:href="DataSheet1.pdf" id="SM3" mimetype="application/pdf" xmlns:xlink="http://www.w3.org/1999/xlink"/>
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<sec id="s13">
<title>Abbreviations</title>
<p>LDH, lumbar disc herniation; PRP, platelet-rich plasma; PELD, percutaneous endoscopic lumbar discectomy; VAS, visual analogue score; IDH, intervertebral disc height; IDP, intervertebral disc protrusion; ODI, Oswestry disability index; JOA, Japanese Orthopaedic Association; SCSA, spinal canal cross-sectional area; RVG, ratio value of disc grey scales; WMD, weighted mean difference; CI, confidence intervals; OR, odds ratio.</p>
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